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George H Sakorafas, Helmut Friess, and George Peros

Association of pheochromocytoma with carcinoma of the thyroid gland . American Journal of Medicine 31 163 – 166 . Skinner MA 2003 Management of hereditary thyroid cancer in children . Surgical Oncology 12 101 – 104 . Skinner MA DeBenedetti

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Maya B Lodish, Karen T Adams, Thanh T Huynh, Tamara Prodanov, Alex Ling, Clara Chen, Suzanne Shusterman, Camilo Jimenez, Maria Merino, Marybeth Hughes, Kendall W Cradic, Dragana Milosevic, Ravinder J Singh, Constantine A Stratakis, and Karel Pacak

: should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? Journal of Clinical Endocrinology and Metabolism 91 2851 – 2858 . Ladroue C Carcenac R Leporrier M Gad S Le Hello C Galateau

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Pamela Brock, Jennifer L Geurts, Paulien Van Galen, Erica Blouch, James Welch, Amy Kunz, Lauren Desrosiers, Jennifer Gauerke, and Samuel Hyde

diseases is owed, in part, to the high hereditary burden associated with certain endocrine diagnoses such as medullary thyroid carcinoma (MTC) and pheochromocytoma/paraganglioma (PCC/PGL). Although the recognition of inherited endocrine disease dates back

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Andreas Machens, Steffen Hauptmann, and Henning Dralle

Introduction Representing an excellent model of genotype–phenotype relationships in hereditary tumors, multiple endocrine neoplasia type 2A (MEN 2A) continues to arouse the keen interest of basic scientists and clinical researchers. Over the past 10

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Annika Blank, Anja M Schmitt, Esther Korpershoek, Francien van Nederveen, Thomas Rudolph, Nicole Weber, Räto Thomas Strebel, Ronald de Krijger, Paul Komminoth, and Aurel Perren

G Huynh TT Pacak K Brouwers FM Walther MM Linehan WM Munson PJ Mannelli M Goldstein DS Elkahloun AG 2004 Distinct gene expression profiles in norepinephrine- and epinephrine-producing hereditary and sporadic pheochromocytomas

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Lucie Evenepoel, Raphaël Helaers, Laurent Vroonen, Selda Aydin, Marc Hamoir, Dominique Maiter, Miikka Vikkula, and Alexandre Persu

assessment of sporadic and hereditary pheochromocytoma . Hormones and Cancer 3 187 – 192 . ( doi:10.1007/s12672-012-0113-y ) 10.1007/s12672-012-0113-y Welander J Andreasson A Juhlin CC Wiseman RW Backdahl M Hoog A Larsson C Gimm O Soderkvist P 2014

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V H M Tsang, T Dwight, D E Benn, G Y Meyer-Rochow, A J Gill, M Sywak, S Sidhu, D Veivers, C M Sue, B G Robinson, R J Clifton-Bligh, and N R Parker

-Medina R Caronia D Pita G 2011 Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma . Nature Genetics 43 663 – 667 . ( doi:10.1038/ng.861 ). Corless CL Schroeder A Griffith D Town A McGreevey L

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Jay S Fonte, Jeremyjones F Robles, Clara C Chen, James Reynolds, Millie Whatley, Alexander Ling, Leilani B Mercado-Asis, Karen T Adams, Victoria Martucci, Tito Fojo, and Karel Pacak

I Leandro-García LJ Letón R Honrado E Ramos-Medina R Caronia D Pita G 2011 Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma . Nature Genetics 43 663 – 667 . doi:10.1038/ng.861 . DeLellis RA

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Alexandru Saveanu, Mihaela Muresan, Catherine De Micco, David Taieb, Anne-Laure Germanetti, Frederic Sebag, Jean-François Henry, Laurent Brunaud, Alain Enjalbert, Georges Weryha, and Anne Barlier

Introduction Pheochromocytomas (PCC) and paragangliomas (PGL) are neuroendocrine tumors derived from adrenal chromaffin cells and extra-adrenal paraganglia respectively ( Eisenhofer et al . 2008 ). These tumors cause variable secondary hypertension

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C Scheuba, K Kaserer, A Moritz, R Drosten, H Vierhapper, C Bieglmayer, O A Haas, and B Niederle

had to be at least twice the basal calcitonin levels ( Barbot et al . 1994 ). Table 1 Demographics – medullary thyroid cancer and C-cell hyperplasia C-cell hyperplasia (only) Medullary thyroid cancer Sporadic Hereditary Σ Sporadic Hereditary Σ N 122