158 related articles for article (PubMed ID: 35984582)
1. Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease.
Bond E; Yashar B; Else T; Osborne J; Marvin M
Fam Cancer; 2023 Apr; 22(2):203-215. PubMed ID: 35984582
[TBL] [Abstract][Full Text] [Related]
2. Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene.
Glushkova M; Dimova P; Yordanova I; Todorov T; Tourtourikov I; Mitev V; Todorova A
Int J Neurosci; 2018 Feb; 128(2):117-124. PubMed ID: 28849724
[TBL] [Abstract][Full Text] [Related]
3. Germline mutations in the new E1' cryptic exon of the
Buffet A; Calsina B; Flores S; Giraud S; Lenglet M; Romanet P; Deflorenne E; Aller J; Bourdeau I; Bressac-de Paillerets B; Calatayud M; Dehais C; De Mones Del Pujol E; Elenkova A; Herman P; Kamenický P; Lejeune S; Sadoul JL; Barlier A; Richard S; Favier J; Burnichon N; Gardie B; Dahia PL; Robledo M; Gimenez-Roqueplo AP
J Med Genet; 2020 Nov; 57(11):752-759. PubMed ID: 31996412
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic investigation of a multi-generational Chinese family afflicted with Von Hippel-Lindau disease.
Zhang J; Ma J; Du X; Wu D; Ai H; Bai J; Dong S; Yang Q; Qu K; Lyu Y; Valenzuela RK; Liu C
Chin Med J (Engl); 2015 Jan; 128(1):32-8. PubMed ID: 25563310
[TBL] [Abstract][Full Text] [Related]
5. VON HIPPEL-LINDAU DISEASE: Update on Pathogenesis and Systemic Aspects.
Aronow ME; Wiley HE; Gaudric A; Krivosic V; Gorin MB; Shields CL; Shields JA; Jonasch EW; Singh AD; Chew EY
Retina; 2019 Dec; 39(12):2243-2253. PubMed ID: 31095066
[TBL] [Abstract][Full Text] [Related]
6. Novel gene mutation in von Hippel-Lindau disease - a report of two cases.
Wang J; Cao W; Wang Z; Zhu H
BMC Med Genet; 2019 Dec; 20(1):194. PubMed ID: 31823746
[TBL] [Abstract][Full Text] [Related]
7. [Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].
Chacón-Camacho OF; Benitez-Granados J; Zenteno JC
Ginecol Obstet Mex; 2013 Apr; 81(4):206-10. PubMed ID: 23720934
[TBL] [Abstract][Full Text] [Related]
8. Characterization of VHL promoter variants in patients suspected of Von Hippel-Lindau disease.
Albanyan S; Giles RH; Gimeno EM; Silver J; Murphy J; Faghfoury H; Morel CF; Machado J; Kim RH
Eur J Med Genet; 2019 Mar; 62(3):177-181. PubMed ID: 30006056
[TBL] [Abstract][Full Text] [Related]
9. Clinical features of pancreatic involvement in von Hippel-Lindau disease: a retrospective study of 55 cases in a single center.
Park TY; Lee SK; Park JS; Oh D; Song TJ; Park DH; Lee SS; Seo DW; Kim MH
Scand J Gastroenterol; 2015 Mar; 50(3):360-7. PubMed ID: 25562111
[TBL] [Abstract][Full Text] [Related]
10. Von Hippel-Lindau disease type 2 in a Chinese family with a VHL p.W88X truncation.
Zhang M; Wang J; Jiang J; Zhan X; Ling Y; Lu Z; Guo J; Gao X
Endocrine; 2015 Feb; 48(1):83-8. PubMed ID: 25069792
[TBL] [Abstract][Full Text] [Related]
11. Sinonasal renal cell-like adenocarcinoma arising in von Hippel Lindau (VHL) syndrome.
Maharaj S; Seegobin K; Wakeman K; Chang S; Potts K; Williams B; Redman R
Oral Oncol; 2022 Feb; 125():105705. PubMed ID: 34998175
[TBL] [Abstract][Full Text] [Related]
12. Pediatric pheochromocytoma in association with Von Hippel-Lindau disease: Focus on screening strategies.
Vérot PL; Rabattu PY; Chabre O; Gayot A; Sartelet H; Faguet R; Robert Y; Piolat C
Arch Pediatr; 2020 Nov; 27(8):497-501. PubMed ID: 33067065
[TBL] [Abstract][Full Text] [Related]
13. Clinical and molecular characteristics of East Asian patients with von Hippel-Lindau syndrome.
Wong M; Chu YH; Tan HL; Bessho H; Ngeow J; Tang T; Tan MH
Chin J Cancer; 2016 Aug; 35(1):79. PubMed ID: 27527340
[TBL] [Abstract][Full Text] [Related]
14. Familial and genetic researches on three Chinese families with von Hippel-Lindau disease.
Mao XC; Su ZP; Yu WQ; Zheng WM; Zeng YJ
Neurol Res; 2009 Sep; 31(7):743-7. PubMed ID: 19133167
[TBL] [Abstract][Full Text] [Related]
15. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma.
Lee JS; Lee JH; Lee KE; Kim JH; Hong JM; Ra EK; Seo SH; Lee SJ; Kim MJ; Park SS; Seong MW
BMC Med Genet; 2016 Jul; 17(1):48. PubMed ID: 27439424
[TBL] [Abstract][Full Text] [Related]
16. De novo VHL germline mutation detected in a patient with mild clinical phenotype of von Hippel-Lindau disease.
Ding X; Zhang C; Frerich JM; Germanwala A; Yang C; Lonser RR; Mao Y; Zhuang Z; Zhang M
J Neurosurg; 2014 Aug; 121(2):384-386. PubMed ID: 24678776
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel-Lindau Disease.
Furness H; Salfity L; Devereux J; Halliday D; Hanson H; Ruddy DM; Uk Vhl Study Group ; Shah N; Sultana G; Woodward ER; Sandford RN; Snape KM; Maher ER
Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573396
[TBL] [Abstract][Full Text] [Related]
19. Mosaicism in von Hippel-Lindau disease with severe renal manifestations.
Wu P; Zhang N; Wang X; Li T; Ning X; Bu D; Gong K
Clin Genet; 2013 Dec; 84(6):581-4. PubMed ID: 23384228
[TBL] [Abstract][Full Text] [Related]
20. Von Hippel-Lindau (VHL) disease: an update on the clinico-pathologic and genetic aspects.
Shehata BM; Stockwell CA; Castellano-Sanchez AA; Setzer S; Schmotzer CL; Robinson H
Adv Anat Pathol; 2008 May; 15(3):165-71. PubMed ID: 18434768
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
