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N B Kiss
N B Kiss
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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J Geli
J Geli
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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F Lundberg
F Lundberg
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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C Avci
C Avci
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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D Velazquez-Fernandez
D Velazquez-Fernandez
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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J Hashemi
J Hashemi
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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G Weber
G Weber
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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A Höög
A Höög
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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T J Ekström
T J Ekström
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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M Bäckdahl
M Bäckdahl
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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C Larsson
C Larsson
Department of Molecular Medicine and Surgery, Department of Clinical Neuroscience, Laboratoire d'Etude des Parasites Génétiques (LEPG), Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital-Solna, CMM L8:01; SE-171 76 Stockholm, Sweden
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phaeochromocytomas . Clinical Endocrinology 45 93 – 96 . Amar L Bertherat J Baudin E Ajzenberg C Bressac-de Paillerets B Chabre O Chamontin B Delemer B Giraud S Murat A 2005 Genetic testing in pheochromocytoma or functional paraganglioma
Patricia L M Dahia
Patricia L M Dahia
Division of Hematology and Medical Oncology, Department of Medicine, Mays Cancer Center, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA
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Roderick Clifton-Bligh
Roderick Clifton-Bligh
Department of Endocrinology, Royal North Shore Hospital, Northern Clinical School, Kolling Institute of Medical Research, University of Sydney, Sydney, New South Wales, Australia
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Anne-Paule Gimenez-Roqueplo
Anne-Paule Gimenez-Roqueplo
AP-HP, Hôpital Européen Georges Pompidou, Genetics Department, Paris, France
Human Cancer Genetics Program, Spanish National Cancer Research Center, Madrid, Spain
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Human Cancer Genetics Program, Spanish National Cancer Research Center, Madrid, Spain
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Mercedes Robledo
Mercedes Robledo
AP-HP, Hôpital Européen Georges Pompidou, Genetics Department, Paris, France
Human Cancer Genetics Program, Spanish National Cancer Research Center, Madrid, Spain
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Human Cancer Genetics Program, Spanish National Cancer Research Center, Madrid, Spain
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Camilo Jimenez
Camilo Jimenez
Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain
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.07.016 ) Favier J Amar L Gimenez-Roqueplo AP 2015 Paraganglioma and phaeochromocytoma: from genetics to personalized medicine . Nature Reviews: Endocrinology 11 101 – 111 . ( https://doi.org/10.1038/nrendo.2014.188 ) Fishbein L Khare S
Sophie Moog
Sophie Moog
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
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Betty Salgues
Betty Salgues
PARCC INSERM UMR970, Paris, France
Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Radiologie, Paris, France
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Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Radiologie, Paris, France
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Yasmine Braik-Djellas
Yasmine Braik-Djellas
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
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Thomas Viel
Thomas Viel
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Daniel Balvay
Daniel Balvay
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Gwennhael Autret
Gwennhael Autret
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
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Estelle Robidel
Estelle Robidel
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
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Anne-Paule Gimenez-Roqueplo
Anne-Paule Gimenez-Roqueplo
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
Plateforme d’Imageries du Vivant, Université de Paris Cité, Faculté de Médecine, Paris, France
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Plateforme d’Imageries du Vivant, Université de Paris Cité, Faculté de Médecine, Paris, France
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Bertrand Tavitian
Bertrand Tavitian
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Génétique, Paris, France
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Sorbonne Université, Service de Médecine Nucléaire, Assistance Publique-Hôpitaux de Paris, Hôpital Pitié Salpêtrière, Paris, France
Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Génétique, Paris, France
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Charlotte Lussey-Lepoutre
Charlotte Lussey-Lepoutre
PARCC INSERM UMR970, Paris, France
Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Radiologie, Paris, France
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Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Radiologie, Paris, France
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Judith Favier
Judith Favier
Université de Paris Cité, PARCC INSERM UMR970, Paris, France
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C 2009 The Warburg effect is genetically determined in inherited pheochromocytomas . PLoS ONE 4 e7094. ( https://doi.org/10.1371/journal.pone.0007094 ) 19763184 Favier J Amar L Gimenez-Roqueplo AP 2015 Paraganglioma and phaeochromocytoma
Aristides Lytras
Aristides Lytras
Division of Endocrinology and Metabolism, Hippocrateion General Hospital, Vas. Sofias 108, GR 115-27 Athens, Greece
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George Tolis
George Tolis
Division of Endocrinology and Metabolism, Hippocrateion General Hospital, Vas. Sofias 108, GR 115-27 Athens, Greece
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Cytogenetics 156 86 – 88 . Hamilton A Sirrs S Schmidt N Onrot J 1997 Anaesthesia for phaeochromocytoma in pregnancy . Canadian Journal of Anaesthesia 44 654 – 657 . Handley J Carson D Sloan J Walsh M Thornton C Hadden D Bingham
Florian Haller
Florian Haller
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Evgeny A Moskalev
Evgeny A Moskalev
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Fabio R Faucz
Fabio R Faucz
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Sarah Barthelmeß
Sarah Barthelmeß
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Stefan Wiemann
Stefan Wiemann
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Matthias Bieg
Matthias Bieg
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Guillaume Assie
Guillaume Assie
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Jerome Bertherat
Jerome Bertherat
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Inga-Marie Schaefer
Inga-Marie Schaefer
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Claudia Otto
Claudia Otto
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Eleanor Rattenberry
Eleanor Rattenberry
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Eamonn R Maher
Eamonn R Maher
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Philipp Ströbel
Philipp Ströbel
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Martin Werner
Martin Werner
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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J Aidan Carney
J Aidan Carney
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Arndt Hartmann
Arndt Hartmann
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Constantine A Stratakis
Constantine A Stratakis
Institute of Pathology University Hospital Erlangen, Friedrich‐Alexander University Erlangen‐Nuremberg, Krankenhausstraße 8-10, D-91054 Erlangen, Germany
Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Program on Developmental Endocrinology and Genetics Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
Division Molecular Genome Analysis
Division of Theoretical Bioinformatics German Cancer Research Center (DKFZ), Heidelberg, Germany
Institut Cochin INSERM U1016, CNRS UMR 8104, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
Department of Endocrinology Referal Center for Rare Adrenal Diseases, Assistance Publique Hôpitaux de Paris, Hôpital Cochin, Paris, France
Institute of Pathology University Medical Center, Georg‐August University, Göttingen, Germany
Institute of Pathology University Hospital, Albert‐Ludwigs University Freiburg, Freiburg, Germany
School of Clinical and Experimental Medicine College of Medical and Dental Sciences, Centre for Rare Diseases and Personalised Medicine, Birmingham Women's Hospital, University of Birmingham and West Midlands Regional Genetics Service, Birmingham, UK
Department of Medical Genetics University of Cambridge, Cambridge CB2 0QQ, UK
Laboratory Medicine and Pathology Emeritus Staff, Mayo Clinic, Rochester, Minnesota, USA
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Abbas Agaimy
Abbas Agaimy
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Korpershoek E Oldenburg RA de Bruyn EM Sleddens HF Derkx P Rivière J Dannenberg H 2009 An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a
Anne-Paule Gimenez-Roqueplo
Anne-Paule Gimenez-Roqueplo
Université Paris Cité, PARCC, INSERM, Paris, France
Département de Médecine Génomique des Tumeurs et des Cancers, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France
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Département de Médecine Génomique des Tumeurs et des Cancers, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France
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Mercedes Robledo
Mercedes Robledo
Hereditary Endocrine Cancer Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain
Biomedical Research Networking Centre on Rare Diseases (CIBERER), Institute of Health Carlos III, Madrid, Spain
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Biomedical Research Networking Centre on Rare Diseases (CIBERER), Institute of Health Carlos III, Madrid, Spain
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Patricia L M Dahia
Patricia L M Dahia
Division of Hematology and Medical Oncology, Department Medicine, University of Texas Health Science Center at San Antonio (UTHSCSA), San Antonio, Texas, USA
Mays Cancer Center at UTHSCSA, San Antonio, Texas, USA
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Mays Cancer Center at UTHSCSA, San Antonio, Texas, USA
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MN Amar L Prejbisz A Robledo M Taieb D Pacak K Crona J Zelinka T Mannelli M 2020 Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the
A Perren
A Perren
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S Schmid
S Schmid
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T Locher
T Locher
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P Saremaslani
P Saremaslani
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C Bonvin
C Bonvin
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P U Heitz
P U Heitz
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P Komminoth
P Komminoth
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Krijger RR, Bruining HA, Lamberts SW, Bonjer HJ, Dinjes WN, Proye C, Koper JW, Bosman FT, Roth J et al. 1998 Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas. International Journal of Cancer
Alberto Cascón
Alberto Cascón
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Lucía Inglada-Pérez
Lucía Inglada-Pérez
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Iñaki Comino-Méndez
Iñaki Comino-Méndez
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Aguirre A de Cubas
Aguirre A de Cubas
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Rocío Letón
Rocío Letón
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Jaume Mora
Jaume Mora
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Mónica Marazuela
Mónica Marazuela
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Juan Carlos Galofré
Juan Carlos Galofré
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Miguel Quesada-Charneco
Miguel Quesada-Charneco
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Mercedes Robledo
Mercedes Robledo
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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Hereditary Endocrine Cancer Group, ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Department of Pediatric Oncology, Endocrinology Division, Department of Endocrinology and Nutrition, Endocrinology Service, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, 28029 Madrid, Spain
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mutations in familial and sporadic paraganglioma and phaeochromocytoma . Lancet Oncology 11 366 – 372 . ( doi:10.1016/S1470-2045(10)70007-3 ). Burnichon N Briere JJ Libe R Vescovo L Riviere J Tissier F Jouanno E Jeunemaitre X Benit P
Raquel G Martins
Raquel G Martins
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Joana B Nunes
Joana B Nunes
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Valdemar Máximo
Valdemar Máximo
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Paula Soares
Paula Soares
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Joana Peixoto
Joana Peixoto
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Telmo Catarino
Telmo Catarino
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Teresa Rito
Teresa Rito
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Pedro Soares
Pedro Soares
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Luísa Pereira
Luísa Pereira
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Manuel Sobrinho-Simões
Manuel Sobrinho-Simões
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Ana Paula Santos
Ana Paula Santos
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Joana Couto
Joana Couto
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Rui Henrique
Rui Henrique
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Joana Matos-Loureiro
Joana Matos-Loureiro
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Paula Dias
Paula Dias
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Isabel Torres
Isabel Torres
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Jorge Lima
Jorge Lima
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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IPATIMUP (Institute of Pathology and Molecular Immunology of the University of Porto), Medical Faculty of the University of Porto, Department of Endocrinology, Department of Pathology, Department of Pathology, Rua Dr Roberto Frias s/n, 4200-465, Porto, Portugal
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Dear Editor We would like to report a genetic screening of SDHB , SDHC , SDHD and SDHAF2 genes (hereafter abbreviated to SDHx ) in patients with paragangliomas (PGL) and phaeochromocytomas (PCC) from northern Portugal. PGL and PCC are
James F H Pittaway
James F H Pittaway
Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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Constantinos Lipsos
Constantinos Lipsos
Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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Katia Mariniello
Katia Mariniello
Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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Leonardo Guasti
Leonardo Guasti
Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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termed ‘ pG2 ’ that had higher expression in phaeochromocytoma compared with neuroblastoma. It became referred to as ‘human adrenal specific cDNA pG2 ’ as it was also shown to be highly expressed in both normal adrenal medulla and cortex ( Helman et al
