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Journal Abstract Search

324 related items for PubMed ID: 19784914

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  • 8. 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
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  • 9. Neuroendocrine tumor of the pancreas and bilateral adrenal pheochromocytomas. A rare manifestation of von Hippel-Lindau disease in childhood.
    Langrehr JM, Bahra M, Kristiansen G, Neumann HP, Neumann LM, Plöckinger U, Lopez-Hänninen E.
    J Pediatr Surg; 2007 Jul; 42(7):1291-4. PubMed ID: 17618900
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  • 10. A rare case of Von Hippel Lindau disease.
    Rohana AG, Norazmi MK, Norlaila M.
    Med J Malaysia; 2006 Jun; 61(2):254-7. PubMed ID: 16898326
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  • 16. Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease?
    Tisherman SE, Tisherman BG, Tisherman SA, Dunmire S, Levey GS, Mulvihill JJ.
    Arch Intern Med; 1993 Nov 22; 153(22):2550-6. PubMed ID: 8239848
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  • 20. 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 22; 162(3 Pt 1):659-64. PubMed ID: 10458336
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