Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease-Reference-Cited by-同舟云学术

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

Published:2017-05-12 Issue:8 Volume:102 Page:2836-2843
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Faucz Fabio R,Tirosh Amit,Tatsi Christina,Berthon Annabel,Hernández-Ramírez Laura C,Settas Nikolaos,Angelousi Anna,Correa Ricardo,Papadakis Georgios Z,Chittiboina Prashant,Quezado Martha,Pankratz Nathan,Lane John,Dimopoulos Aggeliki,Mills James L,Lodish Maya,Stratakis Constantine A

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/102/8/2836/19452660/jc.2017-00161.pdf

Reference29 articles.

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2. Paediatric Cushing’s syndrome: epidemiology, investigation and therapeutic advances;Trends Endocrinol Metab,2007

3. Facial plethora: modern technology for quantifying an ancient clinical sign and its use in Cushing syndrome;J Clin Endocrinol Metab,2015

4. Skin manifestations of Cushing disease in children and adolescents before and after the resolution of hypercortisolemia;Pediatr Dermatol,1998

5. Effects of Cushing disease on bone mineral density in a pediatric population;J Pediatr,2010

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