Zobrazeno 1 - 10
of 289
pro vyhledávání: '"M. Ballmaier"'
Autor:
K. Boztug, U. Baumann, M. Ballmaier, D. Webster, I. Sandrock, R. Jacobs, T. Lion, S. Preuner, M. Germeshausen, G. Hansen, K. Welte, C. Klein
Publikováno v:
Haematologica, Vol 92, Iss 3 (2007)
We report on a 6 year old patient with an unusual clinical presentation of WAS and oligoclonal proliferation of TCRγδ + large granular lymphocytes (LGL). Flow cytometry demonstrated two distinct populations of lymphocytes with strongly decreased (W
Externí odkaz:
https://doaj.org/article/25bc8f08accc4fe4b60546aa761ff899
Autor:
N. Moschny, K. Jahn, H. Maier, A. Khan, K. Liepach, M. Bajbouj, M. Ballmaier, M. Sack, A. Kreitlow, S. Bleich, H. Frieling, A. Neyazi
Publikováno v:
European Neuropsychopharmacology. 29:S438-S439
Publikováno v:
The Journal of Immunology. 156:826-833
Anti-idiotypic vaccination against HIV infection aims at inducing an anti-gp120 immune response through anti-CD4 Abs mimicking epitopes of the gp120 molecule. The mAb IOT4a induces anti-gp120 Abs in rabbits. This study investigates the presence of hu
Autor:
Burghard F. Klapp, P. Georgiewa, H. C. Bauknecht, Georg Bohner, Yvonne Rothemund, Christian von Buchwald, M. Ballmaier, Randolf Klingebiel
Publikováno v:
Neuroscience. 197
Anorexia nervosa is a severe illness and shows one of the highest death rates among psychiatric or psychosomatic diseases. However, despite several lines of research, the etiology of this disease is still unknown. One of those features is the rigidit
Publikováno v:
PPmP - Psychotherapie · Psychosomatik · Medizinische Psychologie. 59
Autor:
M Ballmaier
Publikováno v:
Biological Psychiatry.
Publikováno v:
Annals of the New York Academy of Sciences. 996
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 c-mpl mutations are the cause not only for the hypo
[Congenital amegakaryocytic thrombocytopenia (CAMT) - a defect of the thrombopoietin receptor c-Mpl]
Publikováno v:
Klinische Padiatrie. 213(4)
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 marrow transplant
Akademický článek
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Publikováno v:
Klinische Padiatrie. 208(4)
Thrombopoietin (TPO) belongs to the family of hematopoietic growth factors. It supports the growth and differentiation of megakaryocytic progenitors and precursors in vitro and in vivo. The predominant site of production of TPO is the liver. However,