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516 related items for PubMed ID: 9158701
1. von Hippel-Lindau gene deletion detected in the stromal cell component of a cerebellar hemangioblastoma associated with von Hippel-Lindau disease. Vortmeyer AO, Gnarra JR, Emmert-Buck MR, Katz D, Linehan WM, Oldfield EH, Zhuang Z. Hum Pathol; 1997 May; 28(5):540-3. PubMed ID: 9158701 [Abstract] [Full Text] [Related]
2. Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomas. Lee JY, Dong SM, Park WS, Yoo NJ, Kim CS, Jang JJ, Chi JG, Zbar B, Lubensky IA, Linehan WM, Vortmeyer AO, Zhuang Z. Cancer Res; 1998 Feb 01; 58(3):504-8. PubMed ID: 9458097 [Abstract] [Full Text] [Related]
3. Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system. Gläsker S, Bender BU, Apel TW, van Velthoven V, Mulligan LM, Zentner J, Neumann HP. J Neurol Neurosurg Psychiatry; 2001 May 01; 70(5):644-8. PubMed ID: 11309459 [Abstract] [Full Text] [Related]
4. DNA-based diagnosis of the von Hippel-Lindau syndrome. Patel RJ, Appukuttan B, Ott S, Wang X, Stout JT. Am J Ophthalmol; 2000 Feb 01; 129(2):258-60. PubMed ID: 10682986 [Abstract] [Full Text] [Related]
6. Meningioma showing VHL gene inactivation in a patient with von Hippel-Lindau disease. Kanno H, Yamamoto I, Yoshida M, Kitamura H. Neurology; 2003 Apr 08; 60(7):1197-9. PubMed ID: 12682336 [Abstract] [Full Text] [Related]
9. Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma. Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Hum Mutat; 1998 Apr 08; 12(6):424-30. PubMed ID: 9829912 [Abstract] [Full Text] [Related]
11. Should endolymphatic sac tumors be considered part of the von Hippel-Lindau complex? Pathology case report. Tibbs RE, Bowles AP, Raila FA, Fratkin JD, Hutchins JB. Neurosurgery; 1997 Apr 08; 40(4):848-55; discussion 855. PubMed ID: 9092862 [Abstract] [Full Text] [Related]
17. Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) gene. Hes F, Zewald R, Peeters T, Sijmons R, Links T, Verheij J, Matthijs G, Leguis E, Mortier G, van der Torren K, Rosman M, Lips C, Pearson P, van der Luijt R. Hum Genet; 2000 Apr 08; 106(4):425-31. PubMed ID: 10830910 [Abstract] [Full Text] [Related]
18. Developmentally Arrested Basket/Stellate Cells in Postnatal Human Brain as Potential Tumor Cells of Origin for Cerebellar Hemangioblastoma in von Hippel-Lindau Patients. Shively SB, Edwards NA, MacDonald TJ, Johnson KR, Diaz-Rodriguez NM, Merrill MJ, Vortmeyer AO. J Neuropathol Exp Neurol; 2022 Oct 18; 81(11):885-899. PubMed ID: 35980299 [Abstract] [Full Text] [Related]
19. Molecular pathology of eyes with von Hippel-Lindau (VHL) Disease: a review. Chan CC, Collins AB, Chew EY. Retina; 2007 Jan 18; 27(1):1-7. PubMed ID: 17218907 [Abstract] [Full Text] [Related]
20. Childhood cerebellar hemangioblastoma does not predict germline or somatic mutations in the von Hippel-Lindau tumor suppressor gene. Fisher PG, Tontiplaphol A, Pearlman EM, Duffner PK, Hyder DJ, Stolle CA, Vortmeyer AO, Zhuang Z. Ann Neurol; 2002 Feb 18; 51(2):257-60. PubMed ID: 11835384 [Abstract] [Full Text] [Related] Page: [Next] [New Search]