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Items: 1 to 20 of 125

1.

VHL gene inactivation in an endolymphatic sac tumor associated with von Hippel-Lindau disease.

Vortmeyer AO, Choo D, Pack S, Oldfield E, Zhuang Z.

Neurology. 2000 Aug 8;55(3):460. No abstract available.

PMID:
10932304
2.

VHL gene inactivation in an endolymphatic sac tumor associated with von Hippel-Lindau disease.

Kawahara N, Kume H, Ueki K, Mishima K, Sasaki T, Kirino T.

Neurology. 1999 Jul 13;53(1):208-10.

PMID:
10408561
3.

Somatic von Hippel-Lindau gene mutations detected in sporadic endolymphatic sac tumors.

Vortmeyer AO, Huang SC, Koch CA, Governale L, Dickerman RD, McKeever PE, Oldfield EH, Zhuang Z.

Cancer Res. 2000 Nov 1;60(21):5963-5.

4.

Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease.

Manski TJ, Heffner DK, Glenn GM, Patronas NJ, Pikus AT, Katz D, Lebovics R, Sledjeski K, Choyke PL, Zbar B, Linehan WM, Oldfield EH.

JAMA. 1997 May 14;277(18):1461-6.

PMID:
9145719
6.

Should endolymphatic sac tumors be considered part of the von Hippel-Lindau complex? Pathology case report.

Tibbs RE Jr, Bowles AP Jr, Raila FA, Fratkin JD, Hutchins JB.

Neurosurgery. 1997 Apr;40(4):848-55; discussion 855. Review.

PMID:
9092862
7.

von Hippel-Lindau disease: surveillance strategy for endolymphatic sac tumors.

Poulsen ML, Gimsing S, Kosteljanetz M, Møller HU, Brandt CA, Thomsen C, Bisgaard ML.

Genet Med. 2011 Dec;13(12):1032-41. doi: 10.1097/GIM.0b013e31822beab1.

PMID:
21912262
8.

Mutation of von Hippel-Lindau tumor suppressor gene in a sporadic endolymphatic sac tumor.

Hamazaki S, Yoshida M, Yao M, Nagashima Y, Taguchi K, Nakashima H, Okada S.

Hum Pathol. 2001 Nov;32(11):1272-6.

PMID:
11727270
9.

Endolymphatic sac tumor with von Hippel-Lindau disease: report of a case with atypical pathology of endolymphatic sac tumor.

Yang X, Liu XS, Fang Y, Zhang XH, Zhang YK.

Int J Clin Exp Pathol. 2014 Apr 15;7(5):2609-14. eCollection 2014.

10.

Effects of VHL deficiency on endolymphatic duct and sac.

Gläsker S, Lonser RR, Tran MG, Ikejiri B, Butman JA, Zeng W, Maxwell PH, Zhuang Z, Oldfield EH, Vortmeyer AO.

Cancer Res. 2005 Dec 1;65(23):10847-53.

11.

Differential grading of endolymphatic sac tumor extension by virtue of von Hippel-Lindau disease status.

Bambakidis NC, Megerian CA, Ratcheson RA.

Otol Neurotol. 2004 Sep;25(5):773-81.

PMID:
15354010
12.

Endolymphatic sac tumor (aggressive papillary tumor of middle ear and temporal bone): report of two cases with analysis of the VHL gene.

Skalova A, Síma R, Bohus P, Curík R, Lukás J, Michal M.

Pathol Res Pract. 2008;204(8):599-606. doi: 10.1016/j.prp.2008.01.016. Epub 2008 Apr 18.

PMID:
18423895
13.

Endolymphatic sac tumors in von Hippel-Lindau disease: report of three cases.

Codreanu CM, Duet M, Hautefort C, Wassef M, Guichard JP, Giraud S, Richard S, Roqueplo AP, Tran Ba Huy P.

Otol Neurotol. 2010 Jun;31(4):660-4. doi: 10.1097/MAO.0b013e3181d8d863.

PMID:
20351605
14.

Gene symbol: VHL. Disease: Von-Hippel-Lindau syndrome.

Baker DW, Cherches IM, Rothberg PG.

Hum Genet. 2000 Jun;106(6):671. No abstract available.

PMID:
10942119
15.

Von Hippel-Lindau (VHL) gene analysis in Italian families with VHL disease.

Montera M, Bellone E, Ajmar F, Mandich P.

Contrib Nephrol. 1997;122:109-11. No abstract available.

PMID:
9399050
16.

[File no. 41. VHL (von Hippel-Lindau). Tumor suppressor gene].

Soussi T.

Bull Cancer. 2000 Nov;87(11):771-2. French. No abstract available.

17.

[Endolymphatic sac tumor with von Hippel-Lindau disease: report of two cases with testing of von Hippel-Lindau gene].

Su Y, Shen WD, Wang CC, Han WJ, Liu J, Hou ZH, Song ZG, Huang DL, Han DY, Yang SM.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Nov;48(11):913-8. Chinese.

PMID:
24444636
18.

Endolymphatic sac tumor with von Hippel-Lindau disease: report of a case with analysis of von Hippel-Lindau gene and review.

Rao Q, Zhou J, Wang JD, Jin XZ, Ma HH, Lu ZF, Zhou XJ.

Ann Diagn Pathol. 2010 Oct;14(5):361-4. doi: 10.1016/j.anndiagpath.2009.10.001. Epub 2009 Dec 22. Review.

PMID:
20850701
19.

Von Hippel-Lindau syndrome: hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene.

Humphrey JS, Klausner RD, Linehan WM.

Cancer Treat Res. 1996;88:13-39. Review. No abstract available.

PMID:
9239471

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