BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

974 related articles for article (PubMed ID: 28589383)

  • 41. Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations.
    Nielsen SM; Rubinstein WS; Thull DL; Armstrong MJ; Feingold E; Stang MT; Gnarra JR; Carty SE
    Am J Med Genet A; 2011 Jan; 155A(1):168-73. PubMed ID: 21204227
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. 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]  

  • 44. Endocrine manifestations of von Hippel-Lindau disease.
    Cassol C; Mete O
    Arch Pathol Lab Med; 2015 Feb; 139(2):263-8. PubMed ID: 25611110
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Von Hippel-Lindau disease: strategies in early detection (renal-, adrenal-, pancreatic masses).
    Hes FJ; Feldberg MA
    Eur Radiol; 1999; 9(4):598-610. PubMed ID: 10354869
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Intronic mutation of the VHL gene associated with central nervous system hemangioblastomas in two Chinese families with Von Hippel-Lindau disease: case report.
    Liu Z; Zhou J; Li L; Yi Z; Lu R; Li C; Gong K
    BMC Med Genet; 2020 Oct; 21(1):191. PubMed ID: 33004005
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein.
    Fields FR; Suresh N; Hiller M; Freed SD; Haldar K; Lee SW
    PLoS One; 2020; 15(11):e0234100. PubMed ID: 33151962
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A variety of phenotype with R161Q germline mutation of the von Hippel-Lindau tumor suppressor gene in Japanese kindred.
    Iida K; Okimura Y; Takahashi K; Inomata S; Iguchi G; Kaji H; Chihara K
    Int J Mol Med; 2004 Mar; 13(3):401-4. PubMed ID: 14767570
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. 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]  

  • 53. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
    Neumann HP; Berger DP; Sigmund G; Blum U; Schmidt D; Parmer RJ; Volk B; Kirste G
    N Engl J Med; 1993 Nov; 329(21):1531-8. PubMed ID: 8105382
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene.
    Assadi F; Brackbill EL
    Am J Kidney Dis; 2003 Jan; 41(1):E3. PubMed ID: 12500216
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Von hippel-lindau disease: a genetic and clinical review.
    Haddad NM; Cavallerano JD; Silva PS
    Semin Ophthalmol; 2013; 28(5-6):377-86. PubMed ID: 24138046
    [TBL] [Abstract][Full Text] [Related]  

  • 56. VHL mutations linked to type 2C von Hippel-Lindau disease cause extensive structural perturbations in pVHL.
    Knauth K; Cartwright E; Freund S; Bycroft M; Buchberger A
    J Biol Chem; 2009 Apr; 284(16):10514-22. PubMed ID: 19228690
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. von Hippel-Lindau disease: genetic, clinical, and imaging features.
    Choyke PL; Glenn GM; Walther MM; Patronas NJ; Linehan WM; Zbar B
    Radiology; 1995 Mar; 194(3):629-42. PubMed ID: 7862955
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype.
    Chen F; Kishida T; Yao M; Hustad T; Glavac D; Dean M; Gnarra JR; Orcutt ML; Duh FM; Glenn G
    Hum Mutat; 1995; 5(1):66-75. PubMed ID: 7728151
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.
    Tong AL; Zeng ZP; Zhou YR; Yuan T; Cao CX; Zhang J; Li M
    Chin Med Sci J; 2009 Dec; 24(4):197-201. PubMed ID: 20120764
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 49.