BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 9156047)

  • 1. Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma.
    Garcia A; Matias-Guiu X; Cabezas R; Chico A; Prat J; Baiget M; De Leiva A
    Clin Endocrinol (Oxf); 1997 Mar; 46(3):359-63. PubMed ID: 9156047
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.
    Crossey PA; Eng C; Ginalska-Malinowska M; Lennard TW; Wheeler DC; Ponder BA; Maher ER
    J Med Genet; 1995 Nov; 32(11):885-6. PubMed ID: 8592333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genetic study of a large Chinese kindred with von Hippel-Lindau disease.
    Huang YR; Zhang J; Wang JD; Fan XD
    Chin Med J (Engl); 2004 Apr; 117(4):552-7. PubMed ID: 15109448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.
    Rich TA; Jonasch E; Matin S; Waguespack SG; Gombos DS; Santarpia L; Stolle C; Jimenez C
    Cancer Invest; 2008 Jul; 26(6):642-6. PubMed ID: 18584357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.
    Brauch H; Kishida T; Glavac D; Chen F; Pausch F; Höfler H; Latif F; Lerman MI; Zbar B; Neumann HP
    Hum Genet; 1995 May; 95(5):551-6. PubMed ID: 7759077
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau Disease.
    Allen RC; Webster AR; Sui R; Brown J; Taylor CM; Stone EM
    Arch Ophthalmol; 2001 Nov; 119(11):1659-65. PubMed ID: 11709017
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
    Gergics P; Patocs A; Toth M; Igaz P; Szucs N; Liko I; Fazakas F; Szabo I; Kovacs B; Glaz E; Racz K
    Eur J Endocrinol; 2009 Sep; 161(3):495-502. PubMed ID: 19574279
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Familial and genetic study in a large Chinese kindred with von Hippel-Lindau disease and gene mutation analysis].
    Zhang J; Huang YR; Wang JD; Fan XD
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):5-9. PubMed ID: 14767899
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype.
    Alhawari H; Obeidat Z; Wahbeh L; Mismar A; Younis N; Jafar H; Momani M; Alsabatin N; Awidi A; Alhawari H
    Blood Press; 2024 Dec; 33(1):2355268. PubMed ID: 38824681
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
    Woodward ER; Eng C; McMahon R; Voutilainen R; Affara NA; Ponder BA; Maher ER
    Hum Mol Genet; 1997 Jul; 6(7):1051-6. PubMed ID: 9215674
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.
    Neumann HP; Eng C; Mulligan LM; Glavac D; Zäuner I; Ponder BA; Crossey PA; Maher ER; Brauch H
    JAMA; 1995 Oct; 274(14):1149-51. PubMed ID: 7563486
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing.
    Liu F; Calhoun B; Alam MS; Sun M; Wang X; Zhang C; Haldar K; Lu X
    BMC Med Genet; 2020 Feb; 21(1):42. PubMed ID: 32106822
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. von Hippel Lindau disease with colon adenocarcinoma, renal cell carcinoma and adrenal pheochromocytoma.
    Zinnamosca L; Laudisi A; Petramala L; Marinelli C; Roselli M; Vitolo D; Montesani C; Letizia C
    Intern Med; 2013; 52(14):1599-603. PubMed ID: 23857093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.