Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes-Reference-Cited by-同舟云学术

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Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes

Published:2022-03 Issue:1 Volume:33 Page:197-227
ISSN:1046-3976
Container-title:Endocrine Pathology
language:en
Short-container-title:Endocr Pathol

Author:

Nosé Vania,Gill Anthony,Teijeiro José Manuel Cameselle,Perren Aurel,Erickson Lori

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Pathology and Forensic Medicine

Link

https://link.springer.com/content/pdf/10.1007/s12022-022-09705-5.pdf

Reference273 articles.

1. Couvelard A and Scoazec JY (2020) [Inherited tumor syndromes of gastroenteropancreatic and thoracic neuroendocrine neoplasms]. Ann Pathol 40:120-133 https://doi.org/10.1016/j.annpat.2020.01.002

2. Alrezk R, Hannah-Shmouni F and Stratakis CA (2017) MEN4 and CDKN1B mutations: the latest of the MEN syndromes. Endocr Relat Cancer 24:T195-T208 https://doi.org/10.1530/ERC-17-0243

3. Slingerland J and Pagano M (2000) Regulation of the cdk inhibitor p27 and its deregulation in cancer. J Cell Physiol 183:10-7 https://doi.org/10.1002/(SICI)1097-4652(200004)183:1<10::AID-JCP2>3.0.CO;2-I

4. Francis JM, Kiezun A, Ramos AH et al (2013) Somatic mutation of CDKN1B in small intestine neuroendocrine tumors. Nat Genet 45:1483-6 https://doi.org/10.1038/ng.2821

5. Georgitsi M (2010) MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations. Best Pract Res Clin Endocrinol Metab 24:425-37 https://doi.org/10.1016/j.beem.2010.01.001

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