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Jung Soo Lim, Seung-Eun Lee, Jung Hee Kim, Jae Hyeon Kim, and The Korean Adrenal Gland and Endocrine Hypertension Study Group, Korean Endocrine Society

), multiple endocrine neoplasia type 1 ( 13 ), Beckwith–Wiedemann syndrome ( 14 ), Lynch syndrome ( 15 ), and others ( 16 ). Moreover, at least 50–60% of those with ACC show clinical hormone excess; the most common form is hypercortisolism (Cushing syndrome

Open access

Roland Därr, Jonas Kater, Peggy Sekula, Birke Bausch, Tobias Krauss, Christoph Bode, Gerd Walz, Hartmut P Neumann, and Stefan Zschiedrich

Vortmeyer A Mannelli M Goldstein DS Linehan WM Lenders JW , et al . Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes . Journal of Clinical Endocrinology

Open access

Lisette van Alewijk, Kirsten Davidse, Karlijn Pellikaan, Judith van Eck, Anita C S Hokken-Koelega, Theo C J Sas, Sabine Hannema, Aart J van der Lely, and Laura C G de Graaff

.1186/1750-1172-1-34 ) 52 Thakker RV Newey PJ Walls GV Bilezikian J Dralle H Ebeling PR Melmed S Sakurai A Tonelli F Brandi ML Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1) . Journal of Clinical Endocrinology and

Open access

Katherine U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, Sian E Piret, Kreepa G Kooblall, Mark Stevenson, Karine Rizzoti, Michael R Bowl, M Andrew Nesbit, Paul T Christie, William D Fraser, Tertius Hough, Michael P Whyte, Robin Lovell-Badge, and Rajesh V Thakker

endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia . Endocrine-Related Cancer 2009 1313 – 1327 . ( https://doi.org/10.1677/ERC-09