Neumann HP - Search Results

1

Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

Schmidt L, Junker K, Nakaigawa N, Kinjerski T, Weirich G, Miller M, Lubensky I, Neumann HP, Brauch H, Decker J, Vocke C, Brown JA, Jenkins R, Richard S, Bergerheim U, Gerrard B, Dean M, Linehan WM, Zbar B. Schmidt L, et al. Among authors: neumann hp. Oncogene. 1999 Apr 8;18(14):2343-50. doi: 10.1038/sj.onc.1202547. Oncogene. 1999. PMID: 10327054

2

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. Among authors: neumann hp. 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

3

Renal cysts, renal cancer and von Hippel-Lindau disease.

Neumann HP, Zbar B. Neumann HP, et al. Kidney Int. 1997 Jan;51(1):16-26. doi: 10.1038/ki.1997.3. Kidney Int. 1997. PMID: 8995713 Free article. Review. No abstract available.

4

[Molecular diagnosis of the Hippel-Lindau syndrome].

Neumann HP, Brauch H. Neumann HP, et al. Dtsch Med Wochenschr. 1995 Oct 13;120(41):1416. Dtsch Med Wochenschr. 1995. PMID: 7555669 German. No abstract available.

5

Monogenetic hypertension and pheochromocytoma.

Neumann HP, Bender B, Zäuner I, Berger DP, Eng C, Brauch H, Zbar B. Neumann HP, et al. Am J Kidney Dis. 1996 Sep;28(3):329-33. doi: 10.1016/s0272-6386(96)90488-6. Am J Kidney Dis. 1996. PMID: 8804229

6

von Hippel-Lindau disease: a clinical and scientific review.

Maher ER, Neumann HP, Richard S. Maher ER, et al. Among authors: neumann hp. Eur J Hum Genet. 2011 Jun;19(6):617-23. doi: 10.1038/ejhg.2010.175. Epub 2011 Mar 9. Eur J Hum Genet. 2011. PMID: 21386872 Free PMC article. Review.

7

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

8

Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.

Brauch H, Kishida T, Glavac D, Chen F, Pausch F, Höfler H, Latif F, Lerman MI, Zbar B, Neumann HP. Brauch H, et al. Among authors: neumann hp. Hum Genet. 1995 May;95(5):551-6. doi: 10.1007/BF00223868. Hum Genet. 1995. PMID: 7759077

9

Von Hippel-Lindau syndrome.

Neumann HP, Lips CJ, Hsia YE, Zbar B. Neumann HP, et al. Brain Pathol. 1995 Apr;5(2):181-93. doi: 10.1111/j.1750-3639.1995.tb00592.x. Brain Pathol. 1995. PMID: 7670659 Review.

10

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. Among authors: neumann hp. Hum Genet. 1996 Sep;98(3):271-80. doi: 10.1007/s004390050206. Hum Genet. 1996. PMID: 8707293

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