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Journal Abstract Search
327 related items for PubMed ID: 18584357
1. 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 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. von Hippel-Lindau gene mutation in non-syndromic familial pheochromocytomas. Tong AL, Zeng ZP, Li HZ, Yang D, Lu L, Li M, Zhou YR, Zhang J, Chen S, Liang W. Ann N Y Acad Sci; 2006 Aug; 1073():203-7. PubMed ID: 17102088 [Abstract] [Full Text] [Related]
18. Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: the importance of genetic testing. Cruz JB, Fernandes LP, Clara SA, Conde SJ, Perone D, Kopp P, Nogueira CR. Arq Bras Endocrinol Metabol; 2007 Dec; 51(9):1463-7. PubMed ID: 18209888 [Abstract] [Full Text] [Related]
19. Von hippel-lindau disease and erythrocytosis. Capodimonti S, Teofili L, Martini M, Cenci T, Iachininoto MG, Nuzzolo ER, Bianchi M, Murdolo M, Leone G, Larocca LM. J Clin Oncol; 2012 May 01; 30(13):e137-9. PubMed ID: 22393103 [No Abstract] [Full Text] [Related]