S Krukemeier
Overview
Explore the profile of S Krukemeier including associated specialties, affiliations and a list of published articles.
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Articles
3
Citations
117
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Recent Articles
1.
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...
2.
[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...
3.
Ballmaier M, Germeshausen M, Schulze H, Cherkaoui K, Lang S, Gaudig A, et al.
Blood
. 2001 Jan;
97(1):139-46.
PMID: 11133753
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disease presenting with isolated thrombocytopenia in infancy and developing into a pancytopenia in later childhood. Thrombopoietin (TPO) is the main regulator of thrombocytopoiesis...