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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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Introduction Carney triad (CT) is a rare condition with synchronous or metachronous occurrence in a patient of three tumor entities, namely gastric gastrointestinal stromal tumor (GIST), paraganglioma (PGL), and pulmonary chondroma ( Carney et al
E Kim
E Kim
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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E M Rath
E M Rath
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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V H M Tsang
V H M Tsang
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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A P Duff
A P Duff
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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B G Robinson
B G Robinson
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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W B Church
W B Church
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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D E Benn
D E Benn
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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T Dwight
T Dwight
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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R J Clifton-Bligh
R J Clifton-Bligh
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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Cancer Genetics, Department of Endocrinology, Faculty of Pharmacy, Australian Nuclear Science and Technology Organisation, Kolling Institute of Medical Research, Royal North Shore Hospital, and University of Sydney, Sydney, New South Wales, Australia
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Introduction Phaeochromocytoma (PC) and paraganglioma (PGL) are rare neuroendocrine tumours that arise from adrenal glands and extra-adrenal sites respectively ( Amar et al . 2005 , Gimenez-Roqueplo et al . 2012 ). These tumours occur in the
Francesca Branzoli
Francesca Branzoli
Paris Brain Institute - Institut du Cerveau (ICM), Center for Neuroimaging Research (CENIR), Paris, France
Sorbonne University, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France
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Sorbonne University, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France
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Betty Salgues
Betty Salgues
Sorbonne University, nuclear medicine department, Pitié-Salpêtrière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France
Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France
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Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France
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Małgorzata Marjańska
Małgorzata Marjańska
Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, Minnesota, USA
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Marie Laloi-Michelin
Marie Laloi-Michelin
Endocrinology department, Lariboisière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France
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Philippe Herman
Philippe Herman
ENT unit, Lariboisière Hospital, Assistance -Publique Hôpitaux de Paris, Paris-Cité University, INSERM U1141, Paris, France
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Lauriane Le Collen
Lauriane Le Collen
Inserm/CNRS UMR 1283/8199, Pasteur Institute of Lille, EGID, University of Lille, Lille, France
Department of Endocrinology Diabetology, University Hospital Center of Reims, Reims, France
Department of Genetic, University Hospital Center of Reims, Reims, France
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Department of Endocrinology Diabetology, University Hospital Center of Reims, Reims, France
Department of Genetic, University Hospital Center of Reims, Reims, France
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Brigitte Delemer
Brigitte Delemer
Department of Endocrinology Diabetology, University Hospital Center of Reims, Reims, France
CRESTIC EA 3804, University of Reims Champagne Ardenne, UFR Sciences Exactes et Naturelles, Moulin de La Housse, BP 1039, Reims, France
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CRESTIC EA 3804, University of Reims Champagne Ardenne, UFR Sciences Exactes et Naturelles, Moulin de La Housse, BP 1039, Reims, France
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Julien Riancho
Julien Riancho
AP-HP, Hôpital Européen Georges Pompidou, Hypertension Unit, and Reference centre for rare adrenal diseases, Paris, France
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Emmanuelle Kuhn
Emmanuelle Kuhn
Pituitary Unit, Pitié-Salpêtrière Hospital APHP, Sorbonne University, Paris, France
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Christel Jublanc
Christel Jublanc
Pituitary Unit, Pitié-Salpêtrière Hospital APHP, Sorbonne University, Paris, France
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Nelly Burnichon
Nelly Burnichon
Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Laurence Amar
Laurence Amar
AP-HP, Hôpital Européen Georges Pompidou, Hypertension Unit, and Reference centre for rare adrenal diseases, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Judith Favier
Judith Favier
Université Paris Cité, Inserm, PARCC, Paris, France
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Anne-Paule Gimenez-Roqueplo
Anne-Paule Gimenez-Roqueplo
Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Alexandre Buffet
Alexandre Buffet
Département de médecine génomique des tumeurs et des cancers, AP-HP, Hôpital Européen Georges Pompidou, Paris, France
Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Charlotte Lussey-Lepoutre
Charlotte Lussey-Lepoutre
Sorbonne University, nuclear medicine department, Pitié-Salpêtrière Hospital, Assistance -Publique Hôpitaux de Paris, Paris, France
Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France
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Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France
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endocrine neoplasia type 1 (MEN1), Carney complex, and McCune–Albright syndrome X-linked acrogigantism ( Tatsi & Stratakis 2019 ). In addition, Xekouki et al. described an association between PA and paraganglioma (PGL) named ‘the three P association’ (3PAs
Massimo Mannelli
Massimo Mannelli
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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Elena Rapizzi
Elena Rapizzi
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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Rossella Fucci
Rossella Fucci
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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Letizia Canu
Letizia Canu
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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Tonino Ercolino
Tonino Ercolino
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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Michaela Luconi
Michaela Luconi
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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William F Young Jr
William F Young Jr
Endocrinology Unit, Endocrinology Unit, Division of Endocrinology, Department of Experimental and Clinical Biomedical Sciences ‘Mario Serio’, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy
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pheochromocytoma, termed ‘paraganglioma’, was also not linked to any germline mutations and paragangliomas located in the head and neck region (HN-paragangliomas) were considered as separate entities from those located in the abdomen, chest, and pelvis. In 2000
Karel Pacak
Karel Pacak
Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA
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Roderick Clifton-Bligh
Roderick Clifton-Bligh
Department of Endocrinology Royal North Shore Hospital, University of Sydney, Australia
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of pheochromocytoma and paraganglioma. The ISP was originally established in 2005 under the auspices of the National Institutes of Health, Bethesda, USA in 2005. That year, the first meeting was held in the Holiday Inn hotel in Bethesda and brought
Arthur S Tischler
Arthur S Tischler
Department of Pathology and Laboratory Medicine, Department of Pathology, Department of Pathology, Tufts Medical Center, Tufts University School of Medicine, 800 Washington Street, Box 802, Boston, Massachusetts 02111, USA
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Ronald R deKrijger
Ronald R deKrijger
Department of Pathology and Laboratory Medicine, Department of Pathology, Department of Pathology, Tufts Medical Center, Tufts University School of Medicine, 800 Washington Street, Box 802, Boston, Massachusetts 02111, USA
Department of Pathology and Laboratory Medicine, Department of Pathology, Department of Pathology, Tufts Medical Center, Tufts University School of Medicine, 800 Washington Street, Box 802, Boston, Massachusetts 02111, USA
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Department of Pathology and Laboratory Medicine, Department of Pathology, Department of Pathology, Tufts Medical Center, Tufts University School of Medicine, 800 Washington Street, Box 802, Boston, Massachusetts 02111, USA
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, Bausch et al . 2006 ), were known to be associated with pheochromocytomas, all with well-defined syndromic manifestations, and the genetic associations of extra-adrenal paragangliomas had not been determined. The main role of pathology was to make a
Paul Benjamin Loughrey
Paul Benjamin Loughrey
Patrick G Johnston Centre for Cancer Research, Queen’s University, Belfast, UK
Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Federico Roncaroli
Federico Roncaroli
Geoffrey Jefferson Brain Research Centre, Division of Neuroscience and Experimental Psychology, School of Medicine, Manchester University, Manchester, UK
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Estelle Healy
Estelle Healy
Department of Cellular Pathology, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Philip Weir
Philip Weir
Department of Neurosurgery, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Madhu Basetti
Madhu Basetti
Cancer Research UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, UK
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Ruth T Casey
Ruth T Casey
Department of Endocrinology, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK
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Steven J Hunter
Steven J Hunter
Regional Centre for Endocrinology and Diabetes, Royal Victoria Hospital, Belfast Health & Social Care Trust, Belfast, UK
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Márta Korbonits
Márta Korbonits
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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Introduction Primary tumours of adenohypophyseal cells recently suggested to be redefined as pituitary neuroendocrine tumours (PitNETs) can rarely occur in association with paraganglioma (PGL) or phaeochromocytoma. These tumours may develop in
Trisha Dwight
Trisha Dwight
Cancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, St Leonards, New South Wales, Australia
University of Sydney, Sydney, New South Wales, Australia
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University of Sydney, Sydney, New South Wales, Australia
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Edward Kim
Edward Kim
Cancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, St Leonards, New South Wales, Australia
University of Sydney, Sydney, New South Wales, Australia
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University of Sydney, Sydney, New South Wales, Australia
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Karine Bastard
Karine Bastard
Cancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, St Leonards, New South Wales, Australia
University of Sydney, Sydney, New South Wales, Australia
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University of Sydney, Sydney, New South Wales, Australia
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Diana E Benn
Diana E Benn
Cancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, St Leonards, New South Wales, Australia
University of Sydney, Sydney, New South Wales, Australia
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University of Sydney, Sydney, New South Wales, Australia
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Graeme Eisenhofer
Graeme Eisenhofer
Institute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
Department of Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
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Department of Medicine III, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
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Susan Richter
Susan Richter
Institute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
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Massimo Mannelli
Massimo Mannelli
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy
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Elena Rapizzi
Elena Rapizzi
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy
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Aleksander Prejbisz
Aleksander Prejbisz
Department of Hypertension, National Institute of Cardiology, Warsaw, Poland
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Mariola Pęczkowska
Mariola Pęczkowska
Department of Hypertension, National Institute of Cardiology, Warsaw, Poland
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Karel Pacak
Karel Pacak
National Institutes of Health, Bethesda, Maryland, USA
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Roderick Clifton-Bligh
Roderick Clifton-Bligh
Cancer Genetics Laboratory, Kolling Institute, Royal North Shore Hospital, St Leonards, New South Wales, Australia
University of Sydney, Sydney, New South Wales, Australia
Department of Endocrinology, Royal North Shore Hospital, St Leonards, New South Wales, Australia
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University of Sydney, Sydney, New South Wales, Australia
Department of Endocrinology, Royal North Shore Hospital, St Leonards, New South Wales, Australia
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frequently accompanied by illegitimate activation of hypoxia responses at normal oxygen levels (‘pseudohypoxia’, or the Warburg effect) ( Warburg 1956 , Ruan et al. 2009 ). Pheochromocytomas and paragangliomas (PPGLs) are tumors of the adrenal medulla
Jared S Rosenblum
Jared S Rosenblum
Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States
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Herui Wang
Herui Wang
Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States
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Matthew A Nazari
Matthew A Nazari
Eunice Kennedy Shriver National Institute of Child Health and Development, Bethesda, Maryland, United States
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Zhengping Zhuang
Zhengping Zhuang
Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States
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Karel Pacak
Karel Pacak
Eunice Kennedy Shriver National Institute of Child Health and Development, Bethesda, Maryland, United States
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Investigator Award), at the Sixth International Symposium on Pheochromocytoma/Paraganglioma (ISP) held in Prague, Czech Republic on 19–22 October 2022 which gathered the leading experts in every aspect of pheochromocytoma and paraganglioma (PPGL), including
Camilo Jimenez
Camilo Jimenez
Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
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Sasan Fazeli
Sasan Fazeli
Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
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Alejandro Román-Gonzalez
Alejandro Román-Gonzalez
Department of Endocrinology and Diabetes, Universidad de Antioquia, Medellin, Colombia
Department of Endocrinology, Hospital Universitario San Vicente Fundacion, Medellin, Colombia
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Department of Endocrinology, Hospital Universitario San Vicente Fundacion, Medellin, Colombia
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Introduction Pheochromocytomas and paragangliomas are neuroendocrine tumors that make up less than 1% of all endocrine neoplasias. Pheochromocytomas and paragangliomas arise from the adrenal medulla and the extra-adrenal paraganglia
