Alpha 2.0
Login Register
» Authors » M Germeshausen

M Germeshausen

Explore the profile of M Germeshausen including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 17
Citations 211
Followers 0
Related Specialties
Hematology
Oncology
Science
Top 10 Co-Authors
K Welte
M Ballmaier
H Schulze
C Zeidler
S Krukemeier
C Pilz
S Yetgin
A Koc
A Gaudig
G Strauss
Published In
Blood
Leukemia
Ann N Y Acad Sci
Br J Haematol
Klin Padiatr
Affiliations
Soon will be listed here.
Recent Articles
1.
CSF3R mutations in paediatric acute myeloid leukaemia
Scharn N, Ballmaier M, Reinhardt K, Ehlers S, Zimmermann M, Welte K, et al.
Br J Haematol . 2008 Nov; 144(1):140-2. PMID: 19016735
No abstract available.
2.
Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome
Boztug K, Germeshausen M, Diez I, Gulacsy V, Diestelhorst J, Ballmaier M, et al.
Clin Genet . 2008 May; 74(1):68-74. PMID: 18479478
Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency disorder associated with microthrombocytopenia, eczema, autoimmunity and predisposition to malignant lymphoma. Although rare, few cases of somatic mosaicism have been published in...
3.
Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation
Yetgin S, Olcay L, Koc A, Germeshausen M
Leukemia . 2008 Mar; 22(9):1797. PMID: 18354489
No abstract available.
4.
Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations
Yetgin S, Germeshausen M, Touw I, Koc A, Olcay L
Leukemia . 2005 Jun; 19(9):1710-1. PMID: 15973448
No abstract available.
5.
An acquired G-CSF receptor mutation results in increased proliferation of CMML cells from a patient with severe congenital neutropenia
Germeshausen M, Schulze H, Kratz C, Wilkens L, Repp R, Shannon K, et al.
Leukemia . 2005 Feb; 19(4):611-7. PMID: 15729385
Severe congenital neutropenia (CN) is characterized by a maturation arrest of myelopoiesis at the promyelocyte stage. Treatment with pharmacological doses of recombinant human granulocyte colony-stimulating factor (rh-G-CSF) stimulates neutrophil production...
6.
Thrombopoietin is essential for the maintenance of normal hematopoiesis in humans: development of aplastic anemia in patients with congenital amegakaryocytic thrombocytopenia
Ballmaier M, Germeshausen M, Krukemeier S, Welte K
Ann N Y Acad Sci . 2003 Jun; 996:17-25. PMID: 12799278
Recently, we and others could define the molecular cause of the rare disease congenital amegakaryocytic thrombocytopenia (CAMT) as mutations in the c-mpl gene (Blood 97: 139, 2001). We proposed that...
7.
TNF and lymphotoxin-alpha polymorphisms in patients with severe chronic neutropenia
Gavrikova N, Zeidler C, Stanulla M, Germeshausen M, Schwinzer B, Welte K
Int J Hematol . 2002 Jan; 74(4):477-8. PMID: 11794710
No abstract available.
8.
Mutations in the gene encoding neutrophil elastase (ELA2) are not sufficient to cause the phenotype of congenital neutropenia
Germeshausen M, Schulze H, Ballmaier M, Zeidler C, Welte K
Br J Haematol . 2001 Nov; 115(1):222-4. PMID: 11722436
Mutations in the ELA2 gene encoding human neutrophil elastase have been reported recently to be involved in the aetiology of both, cyclic (CyN) and congenital neutropenia (CN). We analysed the...
9.
[Cyclic neutropenia. Detection of a mutation in the gene for neutrophil elastase (ELA2)]
Schiller M, Bohm M, Zeidler C, Germeshausen M, Welte K, Luger T, et al.
Hautarzt . 2001 Sep; 52(9):790-6. PMID: 11572070
Background And Objective: Cyclic neutropenia is a rare congenital hematopoietic disease which occurs sporadically or as an autosomal dominantly inherited disorder. Recently, the locus for cyclic neutropenia was mapped to...
10.
[Congenital amegakaryocytic thrombocytopenia (CAMT) - a defect of the thrombopoietin receptor c-Mpl]
Germeshausen M, Schulze H, Gaudig A, Krukemeier S, Strauss G, Welte K, et al.
Klin Padiatr . 2001 Aug; 213(4):155-61. PMID: 11528548
Congenital amegakaryocytic thrombocytopenia (CAMT) is a very rare bone marrow failure syndrome presenting with isolated hypomegakaryocytic thrombocytopenia at birth developing into a pancytopenia during the first years of life. Bone...