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Constantine A. Stratakis

Researcher at National Institutes of Health

Publications -  759
Citations -  37973

Constantine A. Stratakis is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Carney complex & PRKAR1A. The author has an hindex of 92, co-authored 716 publications receiving 33374 citations. Previous affiliations of Constantine A. Stratakis include Memorial Sloan Kettering Cancer Center & Nuclear Regulatory Commission.

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Cushing's syndrome

TL;DR: The current understanding of pathogenesis, clinical features, diagnostic, and differential diagnostic approaches, and diagnostic algorithms and recommendations for management of Cushing's syndrome are reviewed.
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Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

TL;DR: The SOST gene, which is mutated in sclerosteosis patients, encodes a protein with a signal peptide for secretion and a cysteine-knot motif that might become an important tool in the development of therapeutic strategies for osteoporosis.
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Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

TL;DR: It is concluded that germline mutations in PRKAR1A, an apparent tumour-suppressor gene, are responsible for the CNC phenotype in a subset of patients with this disease.
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Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline.

TL;DR: A low diagnostic threshold in acutely ill patients, as well as in patients with predisposing factors, is suggested for pregnant women with unexplained persistent nausea, fatigue, and hypotension and a short corticotropin test is recommended as the "gold standard" diagnostic tool to establish the diagnosis.
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Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation

TL;DR: The clinical manifestations of Carney complex are summarized from a worldwide collection of affected patients and an estimate of penetrance and recommendations for genetic screening are provided.