Zur Stadt U - Search Results

1

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.

Zur Stadt U, Beutel K, Kolberg S, Schneppenheim R, Kabisch H, Janka G, Hennies HC. Zur Stadt U, et al. Hum Mutat. 2006 Jan;27(1):62-8. doi: 10.1002/humu.20274. Hum Mutat. 2006. PMID: 16278825

2

[Minimal residual disease analysis in acute lymphoblastic leukemia of childhood within the framework of COALL Study: results of an induction therapy without asparaginase].

zur Stadt U, Harms DO, Schlüter S, Jorch N, Spaar HJ, Nürnberger W, Völpel S, Gutjahr P, Schrappe M, Janka G, Kabisch H. zur Stadt U, et al. Klin Padiatr. 2000 Jul-Aug;212(4):169-73. doi: 10.1055/s-2000-9672. Klin Padiatr. 2000. PMID: 10994545 Clinical Trial. German.

3

MRD at the end of induction therapy in childhood acute lymphoblastic leukemia: outcome prediction strongly depends on the therapeutic regimen.

zur Stadt U, Harms DO, Schlüter S, Schrappe M, Goebel U, Spaar H, Janka G, Kabisch H. zur Stadt U, et al. Leukemia. 2001 Feb;15(2):283-5. doi: 10.1038/sj.leu.2402019. Leukemia. 2001. PMID: 11236947 No abstract available.

4

Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis.

Clementi R, zur Stadt U, Savoldi G, Varoitto S, Conter V, De Fusco C, Notarangelo LD, Schneider M, Klersy C, Janka G, Danesino C, Aricò M. Clementi R, et al. Among authors: zur stadt u. J Med Genet. 2001 Sep;38(9):643-6. doi: 10.1136/jmg.38.9.643. J Med Genet. 2001. PMID: 11565555 Free PMC article. No abstract available.

5

Denaturing HPLC for identification of clonal T-cell receptor gamma rearrangements in newly diagnosed acute lymphoblastic leukemia.

zur Stadt U, Rischewski J, Schneppenheim R, Kabisch H. zur Stadt U, et al. Clin Chem. 2001 Nov;47(11):2003-11. Clin Chem. 2001. PMID: 11673369

6

Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH).

zur Stadt U, Pruggmayer M, Jung H, Henter JI, Schneider M, Kabisch H, Janka G. zur Stadt U, et al. Prenat Diagn. 2002 Jan;22(1):80-1. doi: 10.1002/pd.231. Prenat Diagn. 2002. PMID: 11810660 No abstract available.

7

Rapid LightCycler assay for identification of the perforin codon 374 Trp --> stop mutation in patients and families with hemophagocytic lymphohistiocytosis (HLH).

zur Stadt U, Kabisch H, Janka G, Schneider EM. zur Stadt U, et al. Med Pediatr Oncol. 2003 Jul;41(1):26-9. doi: 10.1002/mpo.10310. Med Pediatr Oncol. 2003. PMID: 12764739

8

Identification and characterisation of clonal incomplete T-cell-receptor Vdelta2-Ddelta3/Ddelta2-Ddelta3 rearrangements by denaturing high-performance liquid chromatography and subsequent fragment collection: implications for minimal residual disease monitoring in childhood acute lymphoblastic leukemia.

zur Stadt U, Eckert C, Rischewski J, Michael K, Golta S, Müller M, Schneppenheim R, Kabisch H. zur Stadt U, et al. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jul 25;792(2):287-98. doi: 10.1016/s1570-0232(03)00318-0. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12860036

9

A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.

Zur Stadt U, Beutel K, Weber B, Kabisch H, Schneppenheim R, Janka G. Zur Stadt U, et al. Blood. 2004 Sep 15;104(6):1909; author reply 1910. doi: 10.1182/blood-2004-02-0733. Blood. 2004. PMID: 15342365 Free article. No abstract available.

10

Standardized detection of Simian virus 40 by real-time quantitative polymerase chain reaction in pediatric malignancies.

Heinsohn S, Golta S, Kabisch H, zur Stadt U. Heinsohn S, et al. Among authors: zur stadt u. Haematologica. 2005 Jan;90(1):94-9. Haematologica. 2005. PMID: 15642675

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