270 related articles for article (PubMed ID: 11835384)
21. Developmentally Arrested Basket/Stellate Cells in Postnatal Human Brain as Potential Tumor Cells of Origin for Cerebellar Hemangioblastoma in von Hippel-Lindau Patients.
Shively SB; Edwards NA; MacDonald TJ; Johnson KR; Diaz-Rodriguez NM; Merrill MJ; Vortmeyer AO
J Neuropathol Exp Neurol; 2022 Oct; 81(11):885-899. PubMed ID: 35980299
[TBL] [Abstract][Full Text] [Related]
22. Gene symbol: VHL. Disease: von Hippel-Lindau syndrome. Accession #Hd0512.
Mavrogiannis LA; Sheridan EG; Burnell LD; Taylor GR
Hum Genet; 2006 Feb; 118(6):774-5. PubMed ID: 17297680
[No Abstract] [Full Text] [Related]
23. Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.
Decker HJ; Neuhaus C; Jauch A; Speicher M; Ried T; Bujard M; Brauch H; Störkel S; Stöckle M; Seliger B; Huber C
Hum Genet; 1996 Jun; 97(6):770-6. PubMed ID: 8641695
[TBL] [Abstract][Full Text] [Related]
24. Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only.
Hes FJ; McKee S; Taphoorn MJ; Rehal P; van Der Luijt RB; McMahon R; van Der Smagt JJ; Dow D; Zewald RA; Whittaker J; Lips CJ; MacDonald F; Pearson PL; Maher ER
J Med Genet; 2000 Dec; 37(12):939-43. PubMed ID: 11106358
[TBL] [Abstract][Full Text] [Related]
25. The occurrence of cerebellar hemangioblastoma in numerous first degree relatives with von Hippel-Lindau disease.
Wysocka B; Wełnicka-Jaśkiewicz M; Matuszewska K; Słoniewski P; Jassem J; Izycka-Swieszewska E; Borowska-Lehman J; Limon J
Folia Neuropathol; 1999; 37(3):175-8. PubMed ID: 10581854
[TBL] [Abstract][Full Text] [Related]
26. Von Hippel-Lindau disease: the role of gene analysis in affected families.
Riegler P; Huber W; Corradini R; Neumann HP; Glaesker S; Sessa A
Nephron; 2000 Jan; 84(1):95-7. PubMed ID: 10644921
[No Abstract] [Full Text] [Related]
27. Incidence of von Hippel-Lindau disease in hemangioblastoma patients: the University of Tokyo Hospital experience from 1954-1998.
Sora S; Ueki K; Saito N; Kawahara N; Shitara N; Kirino T
Acta Neurochir (Wien); 2001 Sep; 143(9):893-6. PubMed ID: 11685621
[TBL] [Abstract][Full Text] [Related]
28. Analysis of von hippel-lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity.
Gijtenbeek JM; Jacobs B; Sprenger SH; Eleveld MJ; van Kessel AG; Kros JM; Sciot R; van Calenbergh F; Wesseling P; Jeuken JW
J Neurosurg; 2002 Oct; 97(4):977-82. PubMed ID: 12405390
[TBL] [Abstract][Full Text] [Related]
29. An analysis of phenotypic variation in the familial cancer syndrome von Hippel-Lindau disease: evidence for modifier effects.
Webster AR; Richards FM; MacRonald FE; Moore AT; Maher ER
Am J Hum Genet; 1998 Oct; 63(4):1025-35. PubMed ID: 9758595
[TBL] [Abstract][Full Text] [Related]
30. Somatic mosaicism in von Hippel-Lindau Disease.
Murgia A; Martella M; Vinanzi C; Polli R; Perilongo G; Opocher G
Hum Mutat; 2000 Jan; 15(1):114. PubMed ID: 10612832
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomas.
Lee JY; Dong SM; Park WS; Yoo NJ; Kim CS; Jang JJ; Chi JG; Zbar B; Lubensky IA; Linehan WM; Vortmeyer AO; Zhuang Z
Cancer Res; 1998 Feb; 58(3):504-8. PubMed ID: 9458097
[TBL] [Abstract][Full Text] [Related]
33. Hemangioblastoma and mosaic von Hippel Lindau disease: rare presentation and review of the literature.
Whitman A; Damodharan S; Bhatia A; Puccetti D; Iskandar B
Childs Nerv Syst; 2023 May; 39(5):1361-1363. PubMed ID: 36708374
[TBL] [Abstract][Full Text] [Related]
34. An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma.
Muscarella LA; Barbano R; Augello B; Formica V; Micale L; Zelante L; D'Agruma L; Merla G
J Hum Genet; 2007; 52(6):485-491. PubMed ID: 17437055
[TBL] [Abstract][Full Text] [Related]
35. Von Hippel-Lindau disease: delayed presentation as a cerebellar haemangioblastoma in an elderly patient.
Shekhar H; Myles L; Lee M
Br J Neurosurg; 2009 Feb; 23(1):97-8. PubMed ID: 19234919
[TBL] [Abstract][Full Text] [Related]
36. The two-stage mutation model in retinal hemangioblastoma.
Chang JH; Spraul CW; Lynn ML; Drack A; Grossniklaus HE
Ophthalmic Genet; 1998 Sep; 19(3):123-30. PubMed ID: 9810567
[TBL] [Abstract][Full Text] [Related]
37. Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion.
Vortmeyer AO; Huang SC; Pack SD; Koch CA; Lubensky IA; Oldfield EH; Zhuang Z
Oncogene; 2002 Feb; 21(8):1167-70. PubMed ID: 11850836
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. Suprasellar hemangioblastoma in a patient with von Hippel-Lindau disease confirmed by germline mutation study: case report and review of the literature.
Goto T; Nishi T; Kunitoku N; Yamamoto K; Kitamura I; Takeshima H; Kochi M; Nakazato Y; Kuratsu J; Ushio Y
Surg Neurol; 2001 Jul; 56(1):22-6. PubMed ID: 11546565
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
