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Journal Abstract Search

319 related items for PubMed ID: 19649731

  • 1. 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
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  • 5. 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
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  • 6. 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
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  • 9. Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease.
    Piermarocchi S, Lo Giudice G, Pilotto E, Bertoja E, Scaroni C, Martella M, Opocher G, Murgia A.
    Graefes Arch Clin Exp Ophthalmol; 2000 Jul; 238(7):615-20. PubMed ID: 10955664
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  • 12. 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
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  • 13. Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.
    Kang HC, Kim IJ, Park JH, Shin Y, Jang SG, Ahn SA, Park HW, Lim SK, Oh SK, Kim DJ, Lee KW, Choi YS, Park YJ, Lee MR, Kim DW, Park JG.
    Oncol Rep; 2005 Oct; 14(4):879-83. PubMed ID: 16142346
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  • 15. The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.
    Abbott MA, Nathanson KL, Nightingale S, Maher ER, Greenstein RM.
    Am J Med Genet A; 2006 Apr 01; 140(7):685-90. PubMed ID: 16502427
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  • 16. Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.
    Opocher G, Conton P, Schiavi F, Macino B, Mantero F.
    Fam Cancer; 2005 Apr 01; 4(1):13-6. PubMed ID: 15883705
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  • 18. 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 01; 24(4):445-50. PubMed ID: 11510758
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  • 19. Clinical presentation of Von Hippel Lindau syndrome type 2B associated with VHL p.A149S mutation in a large Turkish family.
    Mete T, Berker D, Yilmaz E, Ozgen G, Yalcin Y, Tuna M, Ciliz D, Onen M, Aydin Y, Guler S.
    Endocrine; 2014 Feb 01; 45(1):128-35. PubMed ID: 23673869
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  • 20. 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 01; 17(12 Pt 1):1107-11. PubMed ID: 15607616
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