37 related articles for article (PubMed ID: 16630138)
1. Germ-line mutation analysis in patients with von Hippel-Lindau disease in Japan: an extended study of 77 families.
Yoshida M; Ashida S; Kondo K; Kobayashi K; Kanno H; Shinohara N; Shitara N; Kishida T; Kawakami S; Baba M; Yamamoto I; Hosaka M; Shuin T; Yao M
Jpn J Cancer Res; 2000 Feb; 91(2):204-12. PubMed ID: 10761708
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic diagnosis of von Hippel-Lindau disease: analysis of five Japanese families.
Kanno H; Shuin T; Kondo K; Ito S; Hosaka M; Torigoe S; Fujii S; Tanaka Y; Yamamoto I; Kim I; Yao M
Jpn J Cancer Res; 1996 May; 87(5):423-8. PubMed ID: 8641976
[TBL] [Abstract][Full Text] [Related]
3. Mosaicism in von Hippel-Lindau disease: lessons from kindreds with germline mutations identified in offspring with mosaic parents.
Sgambati MT; Stolle C; Choyke PL; Walther MM; Zbar B; Linehan WM; Glenn GM
Am J Hum Genet; 2000 Jan; 66(1):84-91. PubMed ID: 10631138
[TBL] [Abstract][Full Text] [Related]
4. Sequencing of Von Hippel-Lindau (VHL) Gene from Genomic DNA for Mutation Detection in Italian Patients.
Akanni OE; Ferrari M
EJIFCC; 2006 Mar; 17(1):12-16. PubMed ID: 29795717
[TBL] [Abstract][Full Text] [Related]
5. Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: not a needle in a haystack.
Castro-Teles J; Sousa-Pinto B; Rebelo S; Pignatelli D
Endocr Connect; 2021 Oct; 10(11):R293-R304. PubMed ID: 34596579
[TBL] [Abstract][Full Text] [Related]
6. Detection of large deletions in the VHL gene using a Real-Time PCR with SYBR Green.
Ebenazer A; Rajaratnam S; Pai R
Fam Cancer; 2013 Sep; 12(3):519-24. PubMed ID: 23397066
[TBL] [Abstract][Full Text] [Related]
7. Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for caution.
Eisenhofer G; Vocke CD; Elkahloun A; Huynh TT; Prodanov T; Lenders JW; Timmers HJ; Benhammou JN; Linehan WM; Pacak K
Horm Metab Res; 2012 May; 44(5):343-8. PubMed ID: 22438210
[TBL] [Abstract][Full Text] [Related]
8. Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.
Benhammou JN; Vocke CD; Santani A; Schmidt LS; Baba M; Seyama K; Wu X; Korolevich S; Nathanson KL; Stolle CA; Linehan WM
Genes Chromosomes Cancer; 2011 Jun; 50(6):466-77. PubMed ID: 21412933
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.
Gomy I; Molfetta GA; de Andrade Barreto E; Ferreira CA; Zanette DL; Casali-da-Rocha JC; Silva WA
Fam Cancer; 2010 Dec; 9(4):635-42. PubMed ID: 20567917
[TBL] [Abstract][Full Text] [Related]
10. Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature.
Kunogi M; Kurihara M; Ikegami TS; Kobayashi T; Shindo N; Kumasaka T; Gunji Y; Kikkawa M; Iwakami S; Hino O; Takahashi K; Seyama K
J Med Genet; 2010 Apr; 47(4):281-7. PubMed ID: 20413710
[TBL] [Abstract][Full Text] [Related]
11. A vitronectin M381T polymorphism increases risk of hemangioblastoma in patients with VHL gene defect.
Huang JS; Lin CM; Cheng YC; Hung KL; Chien CC; Chen SK; Chang CJ; Chen CW; Huang CJ
J Mol Med (Berl); 2009 Jun; 87(6):613-22. PubMed ID: 19288063
[TBL] [Abstract][Full Text] [Related]
12. Familial neuroendocrine tumor syndromes: from genetics to clinical practice.
Sakurai A; Katai M; Hashizume K; Fukushima Y
Pituitary; 2006; 9(3):231-6. PubMed ID: 17001463
[TBL] [Abstract][Full Text] [Related]
13. Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families.
Zhang J; Huang Y; Pan J; Liu D; Zhou L; Xue W; Chen Q; Dong B; Xuan H
J Cancer Res Clin Oncol; 2008 Nov; 134(11):1211-8. PubMed ID: 18446368
[TBL] [Abstract][Full Text] [Related]
14. Germline mutations of the VHL gene in seven Chinese families with von Hippel-Lindau disease.
Huang Y; Zhou D; Liu J; Zhou P; Li X; Wang Z
Int J Mol Med; 2012 Jan; 29(1):47-52. PubMed ID: 21972040
[TBL] [Abstract][Full Text] [Related]
15. Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients.
Wu P; Zhang N; Wang X; Ning X; Li T; Bu D; Gong K
J Hum Genet; 2012 Apr; 57(4):238-43. PubMed ID: 22357542
[TBL] [Abstract][Full Text] [Related]
16. Von Hippel-Lindau syndrome. A pleomorphic condition.
Friedrich CA
Cancer; 1999 Dec; 86(11 Suppl):2478-82. PubMed ID: 10630173
[TBL] [Abstract][Full Text] [Related]
17. [Von Hippel-Lindau disease].
Shuin T; Ashida S; Yao M; Kanno H
Nihon Rinsho; 2000 Jul; 58(7):1448-54. PubMed ID: 10921322
[TBL] [Abstract][Full Text] [Related]
18. Detection of germline deletions using real-time quantitative polymerase chain reaction in Japanese patients with von Hippel-Lindau disease.
Hattori K; Teranishi J; Stolle C; Yoshida M; Kondo K; Kishida T; Kanno H; Baba M; Kubota Y; Yao M
Cancer Sci; 2006 May; 97(5):400-5. PubMed ID: 16630138
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]