10095351,11409863,12000816,17922902,20151405,22136840,7728151,8707293,8956040[uid] - Search Results

Year	Number of Results
1995	1
1996	2
1999	1
2001	1
2002	1
2007	1
2010	1
2011	1
2024	0

1

[Retinal capillary angioma. Clinical and molecular genetic studies].

Kreusel KM, Bornfeld N, Bender BU, Neumann L, Foerster MH, Neumann HP. Kreusel KM, et al. Ophthalmologe. 1999 Feb;96(2):71-6. doi: 10.1007/s003470050377. Ophthalmologe. 1999. PMID: 10095351 German.

2

DHPLC-based germline mutation screening in the analysis of the VHL tumor suppressor gene: usefulness and limitations.

Klein B, Weirich G, Brauch H. Klein B, et al. Hum Genet. 2001 May;108(5):376-84. doi: 10.1007/s004390100500. Hum Genet. 2001. PMID: 11409863

3

Germ-line mutations in nonsyndromic pheochromocytoma.

Neumann HP, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith WM, Munk R, Manz T, Glaesker S, Apel TW, Treier M, Reineke M, Walz MK, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier-Woelfle M, Peçzkowska M, Szmigielski C, Eng C; Freiburg-Warsaw-Columbus Pheochromocytoma Study Group. Neumann HP, et al. N Engl J Med. 2002 May 9;346(19):1459-66. doi: 10.1056/NEJMoa020152. N Engl J Med. 2002. PMID: 12000816 Free article.

4

A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C.

Schreinemakers JM, Zonnenberg BA, Höppener JW, Hes FJ, Rinkes IH, Lips CJ. Schreinemakers JM, et al. World J Surg Oncol. 2007 Oct 8;5:112. doi: 10.1186/1477-7819-5-112. World J Surg Oncol. 2007. PMID: 17922902 Free PMC article.

5

Genetic analysis of von Hippel-Lindau disease.

Nordstrom-O'Brien M, van der Luijt RB, van Rooijen E, van den Ouweland AM, Majoor-Krakauer DF, Lolkema MP, van Brussel A, Voest EE, Giles RH. Nordstrom-O'Brien M, et al. Hum Mutat. 2010 May;31(5):521-37. doi: 10.1002/humu.21219. Hum Mutat. 2010. PMID: 20151405

6

Is genetic screening indicated in apparently sporadic pheochromocytomas and paragangliomas?

Iacobone M, Schiavi F, Bottussi M, Taschin E, Bobisse S, Fassina A, Opocher G, Favia G. Iacobone M, et al. Surgery. 2011 Dec;150(6):1194-201. doi: 10.1016/j.surg.2011.09.024. Surgery. 2011. PMID: 22136840

7

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, et al. Chen F, et al. Hum Mutat. 1995;5(1):66-75. doi: 10.1002/humu.1380050109. Hum Mutat. 1995. PMID: 7728151

8

Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe.

Glavac D, Neumann HP, Wittke C, Jaenig H, Masek O, Streicher T, Pausch F, Engelhardt D, Plate KH, Höfler H, Chen F, Zbar B, Brauch H. Glavac D, et al. Hum Genet. 1996 Sep;98(3):271-80. doi: 10.1007/s004390050206. Hum Genet. 1996. PMID: 8707293

9

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.

Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al. Zbar B, et al. Hum Mutat. 1996;8(4):348-57. doi: 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3. Hum Mutat. 1996. PMID: 8956040

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