Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma-Reference-Cited by-同舟云学术

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Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma

Published:1997-03 Issue:3 Volume:46 Page:359-363
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Garcia Arnald,Matias-Guiu Xavier,Cabezas Rosa,Chico Ana,Prat Jaime,Baiget Montserrat,De Leiva Alberto

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.1997.00149.x/fullpdf

Cited by 15 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 VHL/HIF Axis in the Development and Treatment of Pheochromocytoma/Paraganglioma;Frontiers in Endocrinology;2020-11-24

3. Isolated Paraganglioma in a Patient with VHL P.L163F Mutation;AACE Clinical Case Reports;2020-07

4. Unsuspected Von Hippel-Lindau syndrome in acute-onset resistant hypertension;BMJ Case Reports;2018-07-24

5. Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene;International Journal of Neuroscience;2017-09-13

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