Familial pituitary apoplexy as the only presentation of a novel AIP mutation-Reference-Cited by-同舟云学术

Familial pituitary apoplexy as the only presentation of a novel AIP mutation

Published:2013-10 Issue:5 Volume:20 Page:L11-L14
ISSN:1351-0088
Container-title:Endocrine-Related Cancer
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Author:

Xekouki Paraskevi,Mastroyiannis Spyridon A,Avgeropoulos Dimitrios,de la Luz Sierra Maria,Trivellin Giampaolo,Gourgari Evgenia A,Lyssikatos Charalampos,Quezado Martha,Patronas Nicholas,Kanaka-Gantenbein Christina,Chrousos George P,Stratakis Constantine A

Publisher

Bioscientifica

Subject

Cancer Research,Endocrinology,Oncology,Endocrinology, Diabetes and Metabolism

Reference10 articles.

1. Familial Isolated Pituitary Adenomas (FIPA) and the Pituitary Adenoma Predisposition due to Mutations in the Aryl Hydrocarbon Receptor Interacting Protein (AIP) Gene

2. Clinical Characteristics and Therapeutic Responses in Patients with Germ-LineAIPMutations and Pituitary Adenomas: An International Collaborative Study

3. Silent Pituitary Apoplexy: Subclinical Infarction of an Adrenocorticotropin-Producing Pituitary Adenoma&

4. Hemorrhage, necrosis, and apoplexy in pituitary adenomas

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