Schumacher V - Search Results

1

Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.

Royer-Pokora B, Beier M, Henzler M, Alam R, Schumacher V, Weirich A, Huff V. Royer-Pokora B, et al. Among authors: schumacher v. Am J Med Genet A. 2004 Jun 15;127A(3):249-57. doi: 10.1002/ajmg.a.30015. Am J Med Genet A. 2004. PMID: 15150775

2

Two molecular subgroups of Wilms' tumors with or without WT1 mutations.

Schumacher V, Schuhen S, Sonner S, Weirich A, Leuschner I, Harms D, Licht J, Roberts S, Royer-Pokora B. Schumacher V, et al. Clin Cancer Res. 2003 Jun;9(6):2005-14. Clin Cancer Res. 2003. PMID: 12796362

3

Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology.

Royer-Pokora B, Weirich A, Schumacher V, Uschkereit C, Beier M, Leuschner I, Graf N, Autschbach F, Schneider D, von Harrach M. Royer-Pokora B, et al. Among authors: schumacher v. Cancer. 2008 Sep 1;113(5):1080-9. doi: 10.1002/cncr.23672. Cancer. 2008. PMID: 18618575 Free article.

4

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.

Schumacher V, Schneider S, Figge A, Wildhardt G, Harms D, Schmidt D, Weirich A, Ludwig R, Royer-Pokora B. Schumacher V, et al. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3972-7. doi: 10.1073/pnas.94.8.3972. Proc Natl Acad Sci U S A. 1997. PMID: 9108089 Free PMC article.

5

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.

Schumacher V, Schärer K, Wühl E, Altrogge H, Bonzel KE, Guschmann M, Neuhaus TJ, Pollastro RM, Kuwertz-Bröking E, Bulla M, Tondera AM, Mundel P, Helmchen U, Waldherr R, Weirich A, Royer-Pokora B. Schumacher V, et al. Kidney Int. 1998 Jun;53(6):1594-600. doi: 10.1046/j.1523-1755.1998.00948.x. Kidney Int. 1998. PMID: 9607189 Free article.

6

Germline Wilms tumor suppressor gene (WT1) mutation leading to isolated genital malformation without Wilms tumor or nephropathy.

Köhler B, Schumacher V, l'Allemand D, Royer-Pokora B, Grüters A. Köhler B, et al. Among authors: schumacher v. J Pediatr. 2001 Mar;138(3):421-4. doi: 10.1067/mpd.2001.112512. J Pediatr. 2001. PMID: 11241055

7

Effective use of high-dose chemotherapy and autologous stem cell rescue for relapsed adult Wilms' tumor and a novel alteration in intron 1 of the WT1 gene.

Trappe RU, Riess H, Lippek F, Plotkin M, Schumacher V, Royer-Pokora B, Hildebrandt B, Zuber J, Mapara MY, Oertel S, Dörken B. Trappe RU, et al. Among authors: schumacher v. J Pediatr Hematol Oncol. 2004 Dec;26(12):820-3. J Pediatr Hematol Oncol. 2004. PMID: 15591903

8

Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome.

Schumacher V, Gueler B, Looijenga LH, Becker JU, Amann K, Engers R, Dotsch J, Stoop H, Schulz W, Royer-Pokora B. Schumacher V, et al. Mol Reprod Dev. 2008 Sep;75(9):1484-94. doi: 10.1002/mrd.20889. Mol Reprod Dev. 2008. PMID: 18271004

9

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.

Köhler B, Schumacher V, Schulte-Overberg U, Biewald W, Lennert T, l'Allemand D, Royer-Pokora B, Grüters A. Köhler B, et al. Among authors: schumacher v. Pediatr Res. 1999 Feb;45(2):187-90. doi: 10.1203/00006450-199902000-00005. Pediatr Res. 1999. PMID: 10022588

10

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Hum Genet. 2005 May;116(6):541. Hum Genet. 2005. PMID: 15991322 No abstract available.

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