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Université de Paris, Paris, France
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Department of Nuclear Medicine, Sorbonne University, Pitie-Salpetriere Hospital, Paris, France
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Université de Paris, Paris, France
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-0113 ) Bayley JP Kunst HP Cascon A 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
Barts and the London School of Medicine, Institute of Endocrinology, Centre for Endocrinology, University of London, London EC1M 6BQ, UK
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to the intraoperative use in patients with carcinoid associated right-sided heart failure ( Watson et al . 1990 , Vergani et al . 1998 ). Phaeochromocytomas and paragangliomas arise from chromaffin cells and may occur in sporadic or familial forms
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-associated tumours, e.g. phaeochromocytomas, thyroid tumours and gonadal tumours ( Table 1 ). The basis for these differences remain to be elucidated; however, it is interesting to note that in two of the conventional Men1 +/− models, exon 2 which contains
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Department of Nuclear Medicine and Molecular Imaging, Lausanne University Hospital, Lausanne, Switzerland
Health Technology Assessment Unit, General Directorate, Ente Ospedaliero Cantonale, Bellinzona, Switzerland
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phaeochromocytoma . Endocrine-Related Cancer 97 – 111. ( https://doi.org/10.1677/ERC-10-0211 ) Estevao R Duarte H Lopes F Fernandes J Monteiro E 2015 Peptide receptor radionuclide therapy in head and neck paragangliomas - Report of 14 cases
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Center of Surgery, Department for Vascular Surgery, Diakonissen Hospital of Leipzig, Leipzig, Germany
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, et al. 2014 Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions . Clinical Endocrinology 80 478 – 486 . ( https://doi.org/10.1111/cen
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1st Department of Internal Medicine, Faculty of Medicine, Pavol Jozef Safarik University in Kosice, Kosice, Slovakia
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metabolomic and secretory phenotypes in phaeochromocytoma . Endocrine-Related Cancer 18 97 – 111 . ( doi:10.1677/ERC-10-0211 ) Favier J Buffet A Gimenez-Roqueplo AP 2012 HIF2A mutations in paraganglioma with polycythemia . New England
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gene, in hereditary paraganglioma . Science 287 848 – 851 . Benn DE Robinson BG 2006 Genetic basis of phaeochromocytoma and paraganglioma . Best Practice and Research. Clinical Endocrinology and Metabolism 20 435 – 450 . Benn DE
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Dannenberg H 2009 An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis . Lancet Oncology 10 764 – 771 . ( doi:10
Human Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, Belgium
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Cardiology Department, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium
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.ajhg.2015.11.011 Luchetti A Walsh D Rodger F Clark G Martin T Irving R Sanna M Yao M Robledo M Neumann HP 2015 Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis . International
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Renal and Hypertension Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Division of Medical Oncology and Hematology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Division of Nuclear Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Division of Medical Oncology and Hematology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Division of Endocrine Oncologic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Division of Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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Renal and Hypertension Division, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
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phaeochromocytoma: systematic review and meta-analysis . Clinical Endocrinology 80 487 – 501 . ( doi:10.1111/cen.12341 ) 10.1111/cen.12341 24118038 Vogel J Atanacio AS Prodanov T Turkbey BI Adams K Martucci V Camphausen K Fojo