Molecular Diagnosis and Extracranial Extension in Cushing Disease-Reference-Cited by-同舟云学术

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Molecular Diagnosis and Extracranial Extension in Cushing Disease

Published:2020-09-01 Issue:9 Volume:146 Page:865
ISSN:2168-6181
Container-title:JAMA Otolaryngology–Head & Neck Surgery
language:en
Short-container-title:JAMA Otolaryngol Head Neck Surg

Author:

Hong Christopher S.¹,Murari Keerti²,Gossmann Mona²,Mahajan Amit³,Erson-Omay Zeynep¹,Manes R. Peter⁴,Omay Sacit Bulent¹

Affiliation:

1. Yale School of Medicine, Department of Neurosurgery, New Haven, Connecticut

2. Yale School of Medicine, Section of Endocrinology and Metabolism, Department of Medicine, New Haven, Connecticut

3. Yale School of Medicine, Department of Radiology, New Haven, Connecticut

4. Yale School of Medicine, Division of Otolaryngology, Department of Surgery, New Haven, Connecticut

Publisher

American Medical Association (AMA)

Subject

Otorhinolaryngology,Surgery

Link

https://jamanetwork.com/journals/jamaotolaryngology/articlepdf/2767834/jamaotolaryngology_hong_2020_lo_200009_1600299452.26604.pdf

Reference6 articles.

1. Pituitary apoplexy: considerations on a single center experience and review of the literature.;Giammattei;J Endocrinol Invest,2016

2. Recurrent gain-of-function USP8 mutations in Cushing’s disease.;Ma;Cell Res,2015

3. Mutations in the deubiquitinase gene USP8 cause Cushing’s disease.;Reincke;Nat Genet,2015

4. The USP8 mutational status may predict long-term remission in patients with Cushing’s disease.;Albani;Clin Endocrinol (Oxf),2018

5. Somatic USP8 gene mutations are a common cause of pediatric cushing disease.;Faucz;J Clin Endocrinol Metab,2017

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