Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers.

Hernández-Ramírez, L. C.; Gabrovska, P.; Dénes, J.; Stals, Karen; Trivellin, G.; Tilley, D.; Ferrau, F.; Evanson, J.; Ellard, Sian; Grossman, A. B.; Roncaroli, F.; Gadelha, M. R.; Korbonits, M.

URI

http://hdl.handle.net/11287/618156

Author

Hernández-Ramírez, L. C.

Gabrovska, P.

Dénes, J.

Stals, Karen

Trivellin, G.

Tilley, D.

Ferrau, F.

Evanson, J.

Ellard, Sian

Grossman, A. B.

Roncaroli, F.

Gadelha, M. R.

Korbonits, M.

Date

2015-09

Journal

The Journal of Clinical Endocrinology and Metabolism

Type

Journal Article
Observational Study
Research Support, Non-U.S. Gov't

Publisher

Endocrine Society

DOI

10.1210/jc.2015-1869

Rights

Archived with thanks to The Journal of clinical endocrinology and metabolism

Metadata

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Abstract

Familial isolated pituitary adenoma (FIPA) due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations is an autosomal dominant disease with incomplete penetrance. Clinical screening of apparently unaffected AIP mutation (AIPmut) carriers could identify previously unrecognized disease.

Citation

Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers. 2015, 100 (9):E1242-54 J. Clin. Endocrinol. Metab.

Publisher URL

http://www.ncbi.nlm.nih.gov/pmc/articles/pmid/26186299/

Note

This article is freely available via PubMed Central. Click on the 'Additional Link' above to access the full text.