… Laurence Amar, Jérôme Bertherat, Eric Baudin, Christiane Ajzenberg, Brigitte Bressac-de
Paillerets, Olivier Chabre, Bernard Chamontin, Brigitte Delemer, Sophie Giraud, Arnaud …

Context: The identification of mutations in genes encoding peptides of succinate dehydrogenase
(SDH) in pheochromocytoma/paraganglioma syndromes has necessitated clear …

Context: Germline mutations in SDHx genes cause hereditary paraganglioma. Objective: The
aim of the study was to assess the indications for succinate dehydrogenase (SDH) genetic …

Some studies have indicated that the risk of fragility fractures in men increases as bone
mineral levels decrease, but there is an overlap in the bone mineral density (BMD) …

Context: An association between germline aryl hydrocarbon receptor-interacting protein (AIP)
gene mutations and pituitary adenomas was recently shown. Objective: The objective of …

Context: Familial pituitary adenomas occur rarely in the absence of multiple endocrine
neoplasia type 1 (MEN1) and Carney complex (CNC). Objective: Our objective was to …

Objective: Our aim was to determine whether the clinical features of 21-hydroxylase–deficient
nonclassic adrenal hyperplasia are correlated with either age at symptom onset or age at …

Objectives The French Acromegaly Registry records data of acromegalic patients' since 1992
in French, Belgian (Liège), and Swiss (Lausanne) centers. We studied the prevalence of …

Germline mutations of the RET proto-oncogene are responsible for multiple endocrine neoplasia
type 2, including multiple endocrine type 2A (MEN 2A), type 2B (MEN 2B), and familial …

Background Refractory hypoglycemia in patients with metastatic insulinoma is an important
cause of morbidity and mortality. Everolimus could be a new therapeutic option. Methods …