These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau disease. Zatyka M; da Silva NF; Clifford SC; Morris MR; Wiesener MS; Eckardt KU; Houlston RS; Richards FM; Latif F; Maher ER Cancer Res; 2002 Jul; 62(13):3803-11. PubMed ID: 12097293 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Clear cell chondrosarcoma in Von Hippel-Lindau disease. Dreijerink KMA; van Leeuwaarde RS; Hackeng WM; Giles RH; de Leng WWJ; Jutte PC; Suurmeijer AJH; van Nesselrooij BPM; Brosens LAA Fam Cancer; 2020 Jan; 19(1):41-45. PubMed ID: 31673890 [TBL] [Abstract][Full Text] [Related]
5. [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]
6. 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]
7. Genotype-phenotype correlations in von Hippel-Lindau disease. Ong KR; Woodward ER; Killick P; Lim C; Macdonald F; Maher ER Hum Mutat; 2007 Feb; 28(2):143-9. PubMed ID: 17024664 [TBL] [Abstract][Full Text] [Related]
8. Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease. Chiorean A; Farncombe KM; Delong S; Andric V; Ansar S; Chan C; Clark K; Danos AM; Gao Y; Giles RH; Goldenberg A; Jani P; Krysiak K; Kujan L; Macpherson S; Maher ER; McCoy LG; Salama Y; Saliba J; Sheta L; Griffith M; Griffith OL; Erdman L; Ramani A; Kim RH Hum Mutat; 2022 Sep; 43(9):1268-1285. PubMed ID: 35475554 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Von Hippel-Lindau syndrome: hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene. Humphrey JS; Klausner RD; Linehan WM Cancer Treat Res; 1996; 88():13-39. PubMed ID: 9239471 [No Abstract] [Full Text] [Related]
11. Germline mutations in the von Hippel-Lindau gene in Italian patients. Ciotti P; Garuti A; Gulli R; Ballestrero A; Bellone E; Mandich P Eur J Med Genet; 2009; 52(5):311-4. PubMed ID: 19464396 [TBL] [Abstract][Full Text] [Related]
12. Endolymphatic sac tumor with von Hippel-Lindau disease: report of a case with analysis of von Hippel-Lindau gene and review. Rao Q; Zhou J; Wang JD; Jin XZ; Ma HH; Lu ZF; Zhou XJ Ann Diagn Pathol; 2010 Oct; 14(5):361-4. PubMed ID: 20850701 [TBL] [Abstract][Full Text] [Related]
13. Adrenal adenoma in von Hippel-Lindau syndrome: A case report with review of literature. Palui R; Kamalanathan S; Sahoo J; Dorairajan LN; Badhe B; Gochhait D J Cancer Res Ther; 2019 Mar; 15(Supplement):S163-S166. PubMed ID: 30900640 [TBL] [Abstract][Full Text] [Related]
14. von Hippel-Lindau disease: a clinical and scientific review. Maher ER; Neumann HP; Richard S Eur J Hum Genet; 2011 Jun; 19(6):617-23. PubMed ID: 21386872 [TBL] [Abstract][Full Text] [Related]
15. A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large Family. Sexton A; Rawlings L; McKavanagh G; Simons K; Winship I J Genet Couns; 2015 Dec; 24(6):882-9. PubMed ID: 26323595 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families. Vikkath N; Valiyaveedan S; Nampoothiri S; Radhakrishnan N; Pillai GS; Nair V; Pooleri GK; Mathew G; Menon KN; Ariyannur PS; Pillai AB Fam Cancer; 2015 Dec; 14(4):585-94. PubMed ID: 25952756 [TBL] [Abstract][Full Text] [Related]
19. Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient. Núñez-Martínez PM; Taja-Chayeb L; Ramírez-Otero MA; Fragoso-Ontiveros V; Wegman-Ostrosky T; Cruz-Robles D; Vidal Millán S Bol Med Hosp Infant Mex; 2021 May; 78(4):341-345. PubMed ID: 33938902 [TBL] [Abstract][Full Text] [Related]
20. A novel mutation links to von Hippel-Lindau syndrome in a Chinese family with hemangioblastoma. Fu XM; Zhao SL; Gui JC; Jiang YQ; Shen MN; Su DL; Gu BJ; Wang XQ; Ren QJ; Yin XD; Huang WB; Chen XG Genet Mol Res; 2015 May; 14(2):4513-20. PubMed ID: 25966224 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]