Cutaneous hyperpigmentation and familial gastrointestinal stromal tumour associated with KIT mutation-Reference-Cited by-同舟云学术

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Cutaneous hyperpigmentation and familial gastrointestinal stromal tumour associated with KIT mutation

Published:2018-10-02 Issue:4 Volume:44 Page:418-421
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Wali G. N.¹,Halliday D.²,Dua J.¹,Ieremia E.³,McPherson T.¹,Matin R. N.¹

Affiliation:

1. Department of Dermatology Oxford University Hospitals NHS Foundation Trust OxfordUK

2. Department of Clinical Genetics Oxford University Hospitals NHS Foundation Trust OxfordUK

3. Department of Cellular Pathology Oxford University Hospitals NHS Foundation Trust Oxford UK

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ced.13757

Reference10 articles.

1. Gastrointestinal stromal tumour

2. Inherited gastrointestinal stromal tumor syndromes: mutations, clinical features, and therapeutic implications

3. Pleomorphic Characteristics of a Germ-Line KIT Mutation in a Large Kindred with Gastrointestinal Stromal Tumors, Hyperpigmentation, and Dysphagia

4. Efficacy and Safety of Imatinib Mesylate in Advanced Gastrointestinal Stromal Tumors

5. Analysis of KIT Mutations in Sporadic and Familial Gastrointestinal Stromal Tumors: Therapeutic Implications through Protein Modeling

Cited by 8 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. Surgical Management of Germline Gastrointestinal Stromal Tumor;Annals of Surgical Oncology;2023-04-28

2. Chinese Pedigree with Hereditary Gastrointestinal Stromal Tumors: A Case Report and Literature Review;International Journal of Molecular Sciences;2023-01-03

3. KIT-Associated Familial GIST Syndrome: Response to Tyrosine Kinase Inhibitors and Implications for Risk Management;The Oncologist;2022-07-06

4. Familial gastrointestinal stromal tumors with KIT germline mutation in a Chinese family: A case report;World Journal of Clinical Cases;2022-05-26

5. Case Report: A Missense Mutation of KIT in Hyperpigmentation and Lentigines Unassociated With Systemic Disorders: Report of a Chinese Pedigree and a Literature Review;Frontiers in Medicine;2022-05-25

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