411 related articles for article (PubMed ID: 19574279)
21. Von Hippel-Lindau disease: a single gene, several hereditary tumors.
Crespigio J; Berbel LCL; Dias MA; Berbel RF; Pereira SS; Pignatelli D; Mazzuco TL
J Endocrinol Invest; 2018 Jan; 41(1):21-31. PubMed ID: 28589383
[TBL] [Abstract][Full Text] [Related]
22. Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma.
Lomte N; Kumar S; Sarathi V; Pandit R; Goroshi M; Jadhav S; Lila AR; Bandgar T; Shah NS
Fam Cancer; 2018 Jul; 17(3):441-449. PubMed ID: 29124493
[TBL] [Abstract][Full Text] [Related]
23. Genotype-phenotype correlations in VHL exon deletions.
McNeill A; Rattenberry E; Barber R; Killick P; MacDonald F; Maher ER
Am J Med Genet A; 2009 Oct; 149A(10):2147-51. PubMed ID: 19764026
[TBL] [Abstract][Full Text] [Related]
24. Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease.
Hasani-Ranjbar S; Amoli MM; Ebrahim-Habibi A; Haghpanah V; Hejazi M; Soltani A; Larijani B
Fam Cancer; 2009; 8(4):465-71. PubMed ID: 19649731
[TBL] [Abstract][Full Text] [Related]
25. Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.
Walther MM; Reiter R; Keiser HR; Choyke PL; Venzon D; Hurley K; Gnarra JR; Reynolds JC; Glenn GM; Zbar B; Linehan WM
J Urol; 1999 Sep; 162(3 Pt 1):659-64. PubMed ID: 10458336
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.
Rasmussen A; Nava-Salazar S; Yescas P; Alonso E; Revuelta R; Ortiz I; Canizales-Quinteros S; Tusié-Luna MT; López-López M
J Neurosurg; 2006 Mar; 104(3):389-94. PubMed ID: 16572651
[TBL] [Abstract][Full Text] [Related]
29. [Genetic analysis of a family with Von Hippel-Lindau syndrome].
Lafuente-Sanchis A; Cuevas JM; Alemany P; Cremades A; Zúñiga Á
Rev Esp Patol; 2017; 50(1):64-67. PubMed ID: 29179968
[TBL] [Abstract][Full Text] [Related]
30. Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient.
Gonc N; Engiz O; Neumann HP; Demirbilek H; Ozon A; Alikasifoglu A; Kandemir N
J Pediatr Endocrinol Metab; 2011; 24(1-2):109-12. PubMed ID: 21528828
[TBL] [Abstract][Full Text] [Related]
31. Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.
Bender BU; Gutsche M; Gläsker S; Müller B; Kirste G; Eng C; Neumann HP
J Clin Endocrinol Metab; 2000 Dec; 85(12):4568-74. PubMed ID: 11134110
[TBL] [Abstract][Full Text] [Related]
32. Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene.
Sansó G; Rudaz MC; Levin G; Barontini M
Am J Hypertens; 2004 Dec; 17(12 Pt 1):1107-11. PubMed ID: 15607616
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease.
Frenzel S; Apel TW; Heidemann PH; Zerres K; Neumann HP; Dörr HG
Eur J Pediatr; 2001 Jul; 160(7):421-4. PubMed ID: 11475579
[TBL] [Abstract][Full Text] [Related]
35. The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system.
Gläsker S; Bender BU; Apel TW; Natt E; van Velthoven V; Scheremet R; Zentner J; Neumann HP
J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):758-62. PubMed ID: 10567493
[TBL] [Abstract][Full Text] [Related]
36. Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings.
Fugaru I; Goudie C; Capolicchio JP
Fam Cancer; 2022 Apr; 21(2):229-233. PubMed ID: 33877494
[TBL] [Abstract][Full Text] [Related]
37. p.N78S and p.R161Q germline mutations of the VHL gene are present in von Hippel-Lindau syndrome in two pedigrees.
Qi XP; Liu WT; Li JY; Dai Y; Ma JM; Zhao Y; Fei J; Li F; Shen M; Jin HY; Chen ZG; Du ZF; Chen XL; Zhang XN
Mol Med Rep; 2013 Sep; 8(3):799-805. PubMed ID: 23842656
[TBL] [Abstract][Full Text] [Related]
38. Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.
Olschwang S; Richard S; Boisson C; Giraud S; Laurent-Puig P; Resche F; Thomas G
Hum Mutat; 1998; 12(6):424-30. PubMed ID: 9829912
[TBL] [Abstract][Full Text] [Related]
39. von Hippel-Lindau syndrome.
Chou A; Toon C; Pickett J; Gill AJ
Front Horm Res; 2013; 41():30-49. PubMed ID: 23652669
[TBL] [Abstract][Full Text] [Related]
40. A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytoma.
D'Elia AV; Grimaldi F; Pizzolitto S; De Maglio G; Bregant E; Passon N; Franzoni A; Verrienti A; Tamburrano G; Durante C; Filetti S; Fogolari F; Russo D; Damante G
Clin Endocrinol (Oxf); 2013 Mar; 78(3):391-7. PubMed ID: 22946750
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
