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Tobias Else Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, 2560E MSRB2, 1150 West Medical Center Drive, Ann Arbor, Michigan 48109‐5674, USA

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Nervi Intercostali Origine . Goettingen, Germany: Abram Vandenhoeck Virchow R 1863 Die krankhaften Geschwuelste . Berlin: Hirschwald Watanabe H Burnstock G Jarrott B Louis WJ 1976 Mitochondrial abnormalities in human phaeochromocytoma

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Neil Sharma School of Clinical and Experimental Medicine, School of Cancer Sciences, Institute for Biomedical Research and

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Ashley Martin School of Clinical and Experimental Medicine, School of Cancer Sciences, Institute for Biomedical Research and

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Christopher J McCabe School of Clinical and Experimental Medicine, School of Cancer Sciences, Institute for Biomedical Research and

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. Despite the wealth of potential biomarkers available, only a small number make it to regular clinical use in screening due to a lack of sensitivity or specificity. One area in which a novel screening approach would be of benefit is in phaeochromocytoma and

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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 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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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 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 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 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 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 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 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 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 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

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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 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 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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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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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

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Sophie Moog Université de Paris Cité, PARCC INSERM UMR970, Paris, France

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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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Yasmine Braik-Djellas Université de Paris Cité, PARCC INSERM UMR970, Paris, France

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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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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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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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Estelle Robidel Université de Paris Cité, PARCC INSERM UMR970, Paris, France

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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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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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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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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

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Aristides Lytras Division of Endocrinology and Metabolism, Hippocrateion General Hospital, Vas. Sofias 108, GR 115-27 Athens, Greece

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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

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Florian Haller
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Evgeny A Moskalev
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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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Sarah Barthelmeß
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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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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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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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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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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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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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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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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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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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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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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

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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
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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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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

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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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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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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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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

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A Perren
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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

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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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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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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 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 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 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 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 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 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 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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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

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