Familial case of pheochromocytoma due to Von Hippel Lindau (VHL) gene mutation

被引：0
|
作者：
Bogdanova, Polina S. [1 ]
Kuznetsova, Elvira S. [1 ]
Beltsevich, Dmitry G.
Troshina, Ekaterina A. [2 ]
Melikyan, Maria A. [1 ]
Peterkova, Valentina A. [1 ]
机构：
[1] Endocrinol Res Ctr, Inst Pediat Endocrinol, Moscow, Russia
[2] Endocrinol Res Ctr, Inst Clin Endocrinol, Moscow, Russia
来源：
HORMONE RESEARCH | 2009年 / 72卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：67 / 68
页数：2
相关论文
共 50 条
  • [31] Von Hippel-Lindau disease and pheochromocytoma
    Walther, MM
    Linehan, WM
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (11): : 839 - 840
  • [32] Pheochromocytoma in Von Hippel-Lindau disease
    Hes, FJ
    Höppener, JWM
    Lips, CJM
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (03): : 969 - 974
  • [33] p.Arg82Leu von Hippel-Lindau (VHL) Gene Mutation among Three Members of a Family with Familial Bilateral Pheochromocytoma in India: Molecular Analysis and In Silico Characterization
    John, Anulekha Mary
    George, Priya Doss C.
    Ebenazer, Andrew
    Seshadri, Mandalam Subramaniam
    Nair, Aravindan
    Rajaratnam, Simon
    Pai, Rekha
    PLOS ONE, 2013, 8 (04):
  • [34] Allelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas
    Vortmeyer, AO
    Lubensky, IA
    Fogt, F
    Linehan, WM
    Khettry, U
    Zhuang, ZP
    AMERICAN JOURNAL OF PATHOLOGY, 1997, 151 (04): : 951 - 956
  • [35] Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene
    Glushkova, Maria
    Dimova, Petia
    Yordanova, Iglika
    Todorov, Tihomir
    Tourtourikov, Ivan
    Mitev, Vanyo
    Todorova, Albena
    INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2018, 128 (02) : 117 - 124
  • [36] Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors
    Prowse, AH
    Webster, AR
    Richards, FM
    Richard, S
    Olschwang, S
    Resche, F
    Affara, NA
    Maher, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 60 (04) : 765 - 771
  • [37] In silico VHL Gene Mutation Analysis and Prognosis of Pancreatic Neuroendocrine Tumors in von Hippel-Lindau Disease
    Tirosh, Amit
    el Lakis, Mustapha
    Green, Patience
    Nockel, Pavel
    Patel, Dhaval
    Nilubol, Naris
    Gara, Sudheer Kumar
    Keutgen, Xavier M.
    Linehan, W. Marston
    Kebebew, Electron
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2018, 103 (04): : 1631 - 1638
  • [38] Molecular analysis of the von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: The importance of genetic testing
    Cruz, Juliana B.
    Fernandes, Leonardo P. S.
    Clara, Sueli A.
    Conde, Sandro J.
    Perone, Denise
    Kopp, Peter
    Nogueira, Celia R.
    ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, 2007, 51 (09) : 1463 - 1467
  • [39] Unusual presentation of pheochromocytoma (PCC) and paraganglioma (PGL) in two sisters with von Hippel Lindau disease (VHL)
    Vieites, Ana
    Benitez, Amanda J.
    Rodriguez, Maria Eugenia
    Bignon, Horacio
    Sanso, Gabriela
    HORMONE RESEARCH IN PAEDIATRICS, 2023, 96 : 546 - 547
  • [40] The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma
    Abbott, MA
    Nathanson, KL
    Nightingale, S
    Maher, ER
    Greenstein, RM
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (07) : 685 - 690
12345