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Department of Health Science, Universidad de Alcalá, Madrid, Spain
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Group of Endocrine Disorders, Institut d’Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain
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Group of Endocrine Disorders, Institut d’Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain
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antihypertensive drugs. The rate of intraoperative complications in our study was 33.3%, but no intraoperative or immediate postsurgical death was reported. Despite the significant reduction in morbidity and mortality of the surgery for phaeochromocytoma over
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V Khau Van Kien P Corvol P Plouin PF Jeunemaitre X 2003 Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas . Cancer Research 63 5615 – 5621 . Grogan RH Mitmaker EJ Duh QY 2011
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Klinik für Endokrinologie, Diabetologie und Klinische Ernährung, UniversitätsSpital Zürich, Zürich, Switzerland
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Pathology 28 95 – 102 . ( https://doi.org/10.1007/s12022-017-9473-8 ) 28271381 10.1007/s12022-017-9473-8 Grocott HP 2017 Safety assessments in the avoidance of preoperative alpha-receptor blockade in phaeochromocytoma surgery: the pitfalls of a
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-3891 ) Castinetti F Qi XP Walz MK Maia AL Sanso G Peczkowska M Hasse-Lazar K Links TP Dvorakova S Toledo RA , et al . 2014 Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an
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Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
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Development 13 2658 – 2669 . ( https://doi.org/10.1101/gad.13.20.2658 ) Eisenhofer G Klink B Richter S Lenders JW Robledo M 2017 Metabologenomics of phaeochromocytoma and paraganglioma: an integrated approach for personalised biochemical
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Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden, Technische Universität Dresden, Dresden, Germany
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National Center of Genetics, Laboratoire National de Santé, Dudelange, Luxembourg
German Cancer Consortium, Dresden, Germany
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Faculty of Chemistry and Food Chemistry, School of Science, Technische Universität Dresden, Dresden, Germany
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Division of Endocrinology and Diabetes, Department of Medicine I, University Hospital Würzburg, University of Würzburg, Würzburg, Germany
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Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden, Technische Universität Dresden, Dresden, Germany
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Department of Internal Medicine III, University Hospital Carl Gustav Carus Dresden, Technische Universität Dresden, Dresden, Germany
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NET Unit, ENETS Centre of Excellence, Royal Free Hospital, London, UK
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Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ) and University of Zurich (UZH), Zurich, Switzerland
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Department of Endocrinology, Diabetology and Clinical Nutrition, University Hospital Zurich (USZ) and University of Zurich (UZH), Zurich, Switzerland
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. Frontiers in Oncology 11 747690 . ( https://doi.org/10.3389/fonc.2021.747690 ) 34646780 Druce MR Kaltsas GA Fraenkel M Gross DJ Grossman AB 2009 Novel and evolving therapies in the treatment of malignant phaeochromocytoma: experience with the
Harvard Medical School, Boston, Massachusetts, USA
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Department of Imaging, Dana-Farber Cancer Institute, Boston, Massachusetts, USA
Department of Radiology, Brigham and Women’s Hospital, Boston, Massachusetts, USA
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Department of Pathology, Brigham and Women’s Hospital, Boston, Massachusetts, USA
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Harvard Medical School, Boston, Massachusetts, USA
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in metastatic phaeochromocytoma and paraganglioma . European Journal of Nuclear Medicine and Molecular Imaging 35 725 – 733 . ( https://doi.org/10.1007/s00259-007-0652-6 ) 10.1007/s00259-007-0652-6 Gonias S Goldsby R Matthay KK Hawkins R
Sorbonne University, UMR S 1127, Inserm U 1127, CNRS UMR 7225, ICM, Paris, France
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Paris Cardiovascular Research Center (PARCC), Inserm, Paris, 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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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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Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Université Paris Cité, Inserm, PARCC, Paris, France
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Paris Cardiovascular Research Center (PARCC), Inserm, Paris, France
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and paragangliomas detects SDH deficiency: clinical and pathophysiological implications . Neoplasia 17 55 – 65 . ( https://doi.org/10.1016/j.neo.2014.10.010 ) Iversen K 1952 Acromegaly associated with phaeochromocytoma . Acta Medica Scandinavica
Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Cancer Genetics Laboratory, Department of Endocrinology, Department of Surgery, Department of Anatomical Pathology, Cancer Diagnosis and Oncology Group, Department of Endocrine and Oncology Surgery, Neurogenetics Research Laboratory, Department of ENT Surgery, Department of Neurology, Bill Walsh Translational Cancer Research Laboratory, Kolling Institute of Medical Research
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Sampietro ML Gaal J Korpershoek E Hinojar-Gutierrez A Timmers HJ Hoefsloot LH Hermsen MA 2010 SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma . Lancet Oncology 11 366 – 372 . ( doi:10.1016/S1470
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Department of Endocrinology, Department of Biophysics and Nuclear Medicine, Diagnostic Nuclear Medicine Division, Program in Reproductive and Adult Endocrinology, Department of Nuclear Medicine, Institut Paoli‐Calmettes, La Timone University Hospital, Aix‐Marseille University, Marseille, France
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-MIBG SPECT in the diagnosis and follow-up of phaeochromocytoma and paraganglioma . European Journal of Nuclear Medicine and Molecular Imaging 39 1266 – 1270 . ( doi:10.1007/s00259-012-2119-7 ). Naji M Al-Nahhas A 2012 (68)Ga-labelled peptides in