Stratakis CA

ORCID: 0000-0002-4058-5520 · 2 papers in corpus
2020
Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 Phenotype.
The Journal of clinical endocrinology and metabolism ·doi:10.1210/clinem/dgaa160

ContextGermline loss-of-function CDKN1B gene variants cause the autosomal dominant syndrome of multiple endocrine neoplasia type 4 (MEN4). Even though pituitary neuroendocrine tumors are a well-known component of the syndrome, only 2 cases …

2019
The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme ·doi:10.1055/a-0661-0341

Pituitary adenomas (PA) and pheochromocytomas/paragangliomas (PHEO/PGL) are rare tumors. Although they may co-exist by coincidence, there is mounting evidence that genes predisposing in PHEO/PGL development, may play a role in pituitary tum…