Recurrent Acromegaly in a Patient With a CHEK2 Mutation-Reference-Cited by-同舟云学术

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Recurrent Acromegaly in a Patient With a CHEK2 Mutation

Published:2021-11 Issue: Volume: Page:
ISSN:2376-0605
Container-title:AACE Clinical Case Reports
language:en
Short-container-title:AACE Clinical Case Reports

Author:

Perosevic Milica^ORCID,Martinez-Lage Maria,Swearingen Brooke,Tritos Nicholas A.

Publisher

Elsevier BV

Reference11 articles.

1. Novel insights into pituitary tumorigenesis: genetic and epigenetic mechanisms;Nadhamuni;Endocr Rev,2020

2. CHEK2 germline variants in cancer predisposition: stalemate rather than checkmate;Stolarova;Cells,2020

3. Chek2 mutation in patient with multiple endocrine glands tumors. Case report;Szeliga;Int J Environ Res Public Health,2020

4. Characterization of tumor-associated Chk2 mutations;Wu;J Biol Chem,2001

5. CHEK2∗1100delC homozygosity is associated with a high breast cancer risk in women;Adank;J Med Genet,2011

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Increased Prevalence of Germline Pathogenic CHEK2 Variants in Individuals With Pituitary Adenomas;The Journal of Clinical Endocrinology & Metabolism;2024-04-23

2. Editorial for March/April Issue of AACE Clinical Case Reports;AACE Clinical Case Reports;2022-03

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