Germeshausen M - Search Results

1

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations.

Germeshausen M, Grudzien M, Zeidler C, Abdollahpour H, Yetgin S, Rezaei N, Ballmaier M, Grimbacher B, Welte K, Klein C. Germeshausen M, et al. Blood. 2008 May 15;111(10):4954-7. doi: 10.1182/blood-2007-11-120667. Epub 2008 Mar 12. Blood. 2008. PMID: 18337561 Free article.

2

Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia.

Tidow N, Pilz C, Teichmann B, Müller-Brechlin A, Germeshausen M, Kasper B, Rauprich P, Sykora KW, Welte K. Tidow N, et al. Among authors: germeshausen m. Blood. 1997 Apr 1;89(7):2369-75. Blood. 1997. PMID: 9116280 Free article.

3

Severe congenital neutropenia patients with point mutations in the granulocyte colony-stimulating factor (G-CSF) receptor mRNA express a normal G-CSF receptor protein.

Kasper B, Herbst A, Pilz C, Germeshausen M, Tidow N, Hadam MR, Welte K. Kasper B, et al. Among authors: germeshausen m. Blood. 1997 Oct 1;90(7):2839-41. Blood. 1997. PMID: 9326253 Free article. No abstract available.

4

Thrombopoietin induces the generation of distinct Stat1, Stat3, Stat5a and Stat5b homo- and heterodimeric complexes with different kinetics in human platelets.

Schulze H, Ballmaier M, Welte K, Germeshausen M. Schulze H, et al. Among authors: germeshausen m. Exp Hematol. 2000 Mar;28(3):294-304. doi: 10.1016/s0301-472x(99)00154-x. Exp Hematol. 2000. PMID: 10720694 Free article.

5

c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia.

Ballmaier M, Germeshausen M, Schulze H, Cherkaoui K, Lang S, Gaudig A, Krukemeier S, Eilers M, Strauss G, Welte K. Ballmaier M, et al. Among authors: germeshausen m. Blood. 2001 Jan 1;97(1):139-46. doi: 10.1182/blood.v97.1.139. Blood. 2001. PMID: 11133753 Free article.

6

Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia.

Germeshausen M, Ballmaier M, Schulze H, Welte K, Flohr T, Beiske K, Storm-Mathisen I, Abrahamsen TG. Germeshausen M, et al. Blood. 2001 Feb 1;97(3):829-30. doi: 10.1182/blood.v97.3.829. Blood. 2001. PMID: 11227095 Free article. No abstract available.

7

Time course of increasing numbers of mutations in the granulocyte colony-stimulating factor receptor gene in a patient with congenital neutropenia who developed leukemia.

Tschan CA, Pilz C, Zeidler C, Welte K, Germeshausen M. Tschan CA, et al. Among authors: germeshausen m. Blood. 2001 Mar 15;97(6):1882-4. doi: 10.1182/blood.v97.6.1882. Blood. 2001. PMID: 11238134 Free article.

8

Implications of mutations in hematopoietic growth factor receptor genes in congenital cytopenias.

Germeshausen M, Ballmaier M, Welte K. Germeshausen M, et al. Ann N Y Acad Sci. 2001 Jun;938:305-20; discussion 320-1. doi: 10.1111/j.1749-6632.2001.tb03599.x. Ann N Y Acad Sci. 2001. PMID: 11458519 Review.

9

[Congenital amegakaryocytic thrombocytopenia (CAMT) - a defect of the thrombopoietin receptor c-Mpl].

Germeshausen M, Schulze H, Gaudig A, Krukemeier S, Strauss G, Welte K, Ballmaier M. Germeshausen M, et al. Klin Padiatr. 2001 Jul-Aug;213(4):155-61. doi: 10.1055/s-2001-16846. Klin Padiatr. 2001. PMID: 11528548 Review. German.

10

[Cyclic neutropenia. Detection of a mutation in the gene for neutrophil elastase (ELA2)].

Schiller M, Böhm M, Zeidler C, Germeshausen M, Welte K, Luger TA, Bonsmann G. Schiller M, et al. Among authors: germeshausen m. Hautarzt. 2001 Sep;52(9):790-6. doi: 10.1007/s001050170068. Hautarzt. 2001. PMID: 11572070 German.

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