A Family with Von Hippel-Lindau Disease Revealed by Pheochromocytoma.-Reference-Cited by-同舟云学术

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A Family with Von Hippel-Lindau Disease Revealed by Pheochromocytoma.

Published:2001 Issue:4 Volume:24 Page:445-450
ISSN:0916-9636
Container-title:Hypertension Research
language:
Short-container-title:Hypertens Res

Author:

TOMITA Naruya,MORIGUCHI Atsushi,YAMASAKI Keita,TANIYAMA Yoshiaki,KOTANI Noriko,HASHIYA Naotaka,YOSHIDA Minoru,YAO Masahiro,HIGAKI Jitsuo,OGIHARA Toshio

Publisher

Japanese Society of Hypertension

Subject

Cardiology and Cardiovascular Medicine,Physiology,Internal Medicine

Reference20 articles.

1. Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred

2. Von Hippel-Lindau disease: a genetic study.

3. Von hippel-lindau disease: New strategies in early detection and treatment

4. Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene

5. Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotype

Cited by 3 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. Regulation of tyrosine hydroxylase promoter activity by the von Hippel-Lindau tumor suppressor protein and hypoxia-inducible transcription factors;Journal of Neurochemistry;2003-04-02

2. Two Cases of Pheochromocytoma Associated with Tetralogy of Fallot;Hypertension Research;2003

3. Feocromocitoma bilateral asociado con enfermedad de Von Hippel-Lindau: estudio genético;Cirugía Española;2002-01

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