Zur Stadt U - Search Results

1

Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire.

Ammann S, Lehmberg K, Zur Stadt U, Janka G, Rensing-Ehl A, Klemann C, Heeg M, Bode S, Fuchs I, Ehl S; HLH study of the GPOH. Ammann S, et al. Among authors: zur stadt u. Eur J Immunol. 2017 Feb;47(2):364-373. doi: 10.1002/eji.201646686. Epub 2017 Jan 3. Eur J Immunol. 2017. PMID: 27925643 Free PMC article.

2

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.

3

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.

4

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

5

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.

zur Stadt U, Schmidt S, Kasper B, Beutel K, Diler AS, Henter JI, Kabisch H, Schneppenheim R, Nürnberg P, Janka G, Hennies HC. zur Stadt U, et al. Hum Mol Genet. 2005 Mar 15;14(6):827-34. doi: 10.1093/hmg/ddi076. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703195

6

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

7

Familial and acquired hemophagocytic lymphohistiocytosis.

Janka G, zur Stadt U. Janka G, et al. Among authors: zur stadt u. Hematology Am Soc Hematol Educ Program. 2005:82-8. doi: 10.1182/asheducation-2005.1.82. Hematology Am Soc Hematol Educ Program. 2005. PMID: 16304363

8

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.

Trizzino A, zur Stadt U, Ueda I, Risma K, Janka G, Ishii E, Beutel K, Sumegi J, Cannella S, Pende D, Mian A, Henter JI, Griffiths G, Santoro A, Filipovich A, Aricò M; Histiocyte Society HLH Study group. Trizzino A, et al. Among authors: zur stadt u. J Med Genet. 2008 Jan;45(1):15-21. doi: 10.1136/jmg.2007.052670. Epub 2007 Sep 14. J Med Genet. 2008. PMID: 17873118

9

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.

zur Stadt U, Rohr J, Seifert W, Koch F, Grieve S, Pagel J, Strauss J, Kasper B, Nürnberg G, Becker C, Maul-Pavicic A, Beutel K, Janka G, Griffiths G, Ehl S, Hennies HC. zur Stadt U, et al. Am J Hum Genet. 2009 Oct;85(4):482-92. doi: 10.1016/j.ajhg.2009.09.005. Am J Hum Genet. 2009. PMID: 19804848 Free PMC article.

10

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.

Rohr J, Beutel K, Maul-Pavicic A, Vraetz T, Thiel J, Warnatz K, Bondzio I, Gross-Wieltsch U, Schündeln M, Schütz B, Woessmann W, Groll AH, Strahm B, Pagel J, Speckmann C, Janka G, Griffiths G, Schwarz K, zur Stadt U, Ehl S. Rohr J, et al. Among authors: zur stadt u. Haematologica. 2010 Dec;95(12):2080-7. doi: 10.3324/haematol.2010.029389. Epub 2010 Sep 7. Haematologica. 2010. PMID: 20823128 Free PMC article.

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