Stanulla M - Search Results

1

Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact.

Schütte P, Möricke A, Zimmermann M, Bleckmann K, Reismüller B, Attarbaschi A, Mann G, Bodmer N, Niggli F, Schrappe M, Stanulla M, Kratz CP. Schütte P, et al. Among authors: stanulla m. Eur J Med Genet. 2016 Mar;59(3):143-51. doi: 10.1016/j.ejmg.2015.12.008. Epub 2015 Dec 28. Eur J Med Genet. 2016. PMID: 26732628 Review.

2

Secondary brain tumours in children with ALL.

Stanulla M, Löning L, Welte K, Schrappe M. Stanulla M, et al. Lancet. 1999 Sep 25;354(9184):1126-7. doi: 10.1016/S0140-6736(05)76923-3. Lancet. 1999. PMID: 10509534 No abstract available.

3

Polymorphisms within glutathione S-transferase genes (GSTM1, GSTT1, GSTP1) and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia: a case-control study.

Stanulla M, Schrappe M, Brechlin AM, Zimmermann M, Welte K. Stanulla M, et al. Blood. 2000 Feb 15;95(4):1222-8. Blood. 2000. PMID: 10666194 Free article.

4

Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life.

Stanulla M, Kasper B, Schrappe M, Viehmann S, Harbott J, Ludwig WD, Welte K. Stanulla M, et al. Leukemia. 2000 Feb;14(2):337-8. doi: 10.1038/sj.leu.2401653. Leukemia. 2000. PMID: 10673755 No abstract available.

5

No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence.

Stanulla M, Stümm M, Dieckvoss BO, Seidemann K, Schemmel V, Müller Brechlin A, Schrappe M, Welte K, Reiter A. Stanulla M, et al. Br J Haematol. 2000 Apr;109(1):117-20. doi: 10.1046/j.1365-2141.2000.01973.x. Br J Haematol. 2000. PMID: 10848790 Free article.

6

Polymorphisms within glutathione S-transferase genes and initial response to glucocorticoids in childhood acute lymphoblastic leukaemia.

Anderer G, Schrappe M, Brechlin AM, Lauten M, Muti P, Welte K, Stanulla M. Anderer G, et al. Among authors: stanulla m. Pharmacogenetics. 2000 Nov;10(8):715-26. doi: 10.1097/00008571-200011000-00006. Pharmacogenetics. 2000. PMID: 11186134

7

Tumor necrosis factor and lymphotoxin-alpha genetic polymorphisms and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia: a case-control study of patients treated with BFM therapy.

Stanulla M, Schrauder A, Welte K, Schrappe M. Stanulla M, et al. BMC Blood Disord. 2001;1(1):2. doi: 10.1186/1471-2326-1-2. BMC Blood Disord. 2001. PMID: 11319038 Free PMC article.

8

Clinical outcome of patients with childhood acute lymphoblastic leukaemia and an initial leukaemic blood blast count of less than 1000 per microliter.

Lauten M, Stanulla M, Zimmermann M, Welte K, Riehm H, Schrappe M. Lauten M, et al. Among authors: stanulla m. Klin Padiatr. 2001 Jul-Aug;213(4):169-74. doi: 10.1055/s-2001-16848. Klin Padiatr. 2001. PMID: 11528550 Clinical Trial.

9

Polymorphisms within glutathione S-transferase genes in pediatric non-Hodgkin's lymphoma.

Dieckvoss BO, Stanulla M, Schrappe M, Beier R, Zimmermann M, Welte K, Reiter A. Dieckvoss BO, et al. Among authors: stanulla m. Haematologica. 2002 Jul;87(7):709-13; discussion 713. Haematologica. 2002. PMID: 12091121

10

Association of initial response to prednisone treatment in childhood acute lymphoblastic leukaemia and polymorphisms within the tumour necrosis factor and the interleukin-10 genes.

Lauten M, Matthias T, Stanulla M, Beger C, Welte K, Schrappe M. Lauten M, et al. Among authors: stanulla m. Leukemia. 2002 Aug;16(8):1437-42. doi: 10.1038/sj.leu.2402545. Leukemia. 2002. PMID: 12145682

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