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Journal Abstract Search

181 related items for PubMed ID: 8550742

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  • 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
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  • 11. 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 Jul; 5(1):66-75. PubMed ID: 7728151
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  • 12. 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
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  • 13. Novel human pathological mutations. Gene symbol: VHL. Disease: Von Hippel-Lindau syndrome.
    Ellison J.
    Hum Genet; 2010 Apr; 127(4):477. PubMed ID: 21488287
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  • 14. 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
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  • 18. Genetics of pheochromocytoma and paraganglioma in Spanish patients.
    Cascón A, Pita G, Burnichon N, Landa I, López-Jiménez E, Montero-Conde C, Leskelä S, Leandro-García LJ, Letón R, Rodríguez-Antona C, Díaz JA, López-Vidriero E, González-Neira A, Velasco A, Matias-Guiu X, Gimenez-Roqueplo AP, Robledo M.
    J Clin Endocrinol Metab; 2009 May; 94(5):1701-5. PubMed ID: 19258401
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  • 19. A family with von Hippel-Lindau disease revealed by pheochromocytoma.
    Tomita N, Moriguchi A, Yamasaki K, Taniyama Y, Kotani N, Hashiya N, Yoshida M, Yao M, Higaki J, Ogihara T.
    Hypertens Res; 2001 Jul; 24(4):445-50. PubMed ID: 11510758
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