Clinical diagnosis, treatment and screening of the VHL gene in three von Hippel‑Lindau disease pedigrees-Reference-Cited by-同舟云学术

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Clinical diagnosis, treatment and screening of the VHL gene in three von Hippel‑Lindau disease pedigrees

Published:2020-06-03 Issue:2 Volume:20 Page:1237-1244
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Lin Guobing¹,Zhao Yihua²,Zhang Zhewei³,Zhang Huijiang⁴

Affiliation:

1. Department of Urology, The First People's Hospital of Wenling, Wenling, Zhejiang 317500, P.R. China

2. Department of Urology, Yueqing People's Hospital, Yueqing, Zhejiang 325600, P.R. China

3. Department of Urology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang 310009, P.R. China

4. Department of Urology, Lishui City People's Hospital, Lishui, Zhejiang 323000 P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 6 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. Genetics, Pathophysiology, and Current Challenges in Von Hippel–Lindau Disease Therapeutics;Diagnostics;2024-08-29

2. The genetic differences between types 1 and 2 in von Hippel-Lindau syndrome: comprehensive meta-analysis;BMC Ophthalmology;2024-08-13

3. Analysis of mutations in EPOR, VHL, EPAS1 and EGLN1 genes associated with the familial erythrocytosis ECYT1-4 among JAK2- and CALR-negative patients with the erythrocytosis of unclear etiology;Russian journal of hematology and transfusiology;2023-12-28

4. Retinal hemangioblastoma in a patient with Von Hippel-Lindau disease: A case report and literature review;Frontiers in Oncology;2022-11-02

5. VHL syndrome without clear family history: A rare case report and literature review of Chinese patients;Frontiers in Neurology;2022-10-17

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