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Human Pathology
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December 31, 1997
Expression of fibrinolytic antigens in redistributed cardiac mast cells in auricular thrombosis
H C Bankl, T Radaszkiewicz, B Pikula, et al.
British Journal of Haematology
|
August 8, 1998
Recombinant human megakaryocyte growth and development factor increases levels of circulating haemopoietic progenitor cells post chemotherapy in patients with acute myeloid leukaemia
K Geissler, E Kabrna, S Stengg, et al.
Wiener Klinische Wochenschrift
|
August 3, 1973
[Arterial counterpulsation by means of an interaortic bypass ventricle (author's transl)]
W Fasching, M Deutsch, W Enenkel, et al.
Acta Haematologica
|
January 1, 1982
Systemic candidiasis complicating bone marrow transplantation in aplastic anemia. Case report
W Hinterberger, L Fridrich, W Graninger, et al.
Blood
|
September 15, 1995
Novel CBF beta-MYH11 fusion transcripts and alternative splicing in acute myeloid leukemia with inversion of chromosome 16
M Novak, K Laczika, M Mitterbauer, et al.
Cancer Investigation
|
January 1, 1993
Combination treatment of acute myeloblastic leukemia with rhGM-CSF and standard induction chemotherapy
P Valent, C Sillaber, K Geissler, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 1, 1990
Prognostic significance of surface marker expression on blasts of patients with de novo acute myeloblastic leukemia
I Schwarzinger, P Valent, U Köller, et al.
British Journal of Haematology
|
March 1, 1985
Cell lineage heterogeneity in blast crisis of chronic myeloid leukaemia
P Bettelheim, D Lutz, O Majdic, et al.
The Journal of Clinical Investigation
|
June 1, 1985
Deficiency of the autologous mixed lymphocyte reaction in patients with classic hemophilia treated with commercial factor VIII concentrate. Correlation with T cell subset distribution, antibodies to lymphadenopathy-associated or human T lymphotropic virus, and analysis of the cellular basis of the deficiency
J S Smolen, P Bettelheim, U Köller, et al.
British Journal of Haematology
|
December 31, 1997
A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiency
S Mustafa, I Pabinger, K Vàradi, et al.
Page
of 48
Search research articles
Search
Showing results (291-300 of 478) with videos related to
Sort By:
Page
of 48
Human Pathology
|
December 31, 1997
Expression of fibrinolytic antigens in redistributed cardiac mast cells in auricular thrombosis
H C Bankl, T Radaszkiewicz, B Pikula, et al.
British Journal of Haematology
|
August 8, 1998
Recombinant human megakaryocyte growth and development factor increases levels of circulating haemopoietic progenitor cells post chemotherapy in patients with acute myeloid leukaemia
K Geissler, E Kabrna, S Stengg, et al.
Wiener Klinische Wochenschrift
|
August 3, 1973
[Arterial counterpulsation by means of an interaortic bypass ventricle (author's transl)]
W Fasching, M Deutsch, W Enenkel, et al.
Acta Haematologica
|
January 1, 1982
Systemic candidiasis complicating bone marrow transplantation in aplastic anemia. Case report
W Hinterberger, L Fridrich, W Graninger, et al.
Blood
|
September 15, 1995
Novel CBF beta-MYH11 fusion transcripts and alternative splicing in acute myeloid leukemia with inversion of chromosome 16
M Novak, K Laczika, M Mitterbauer, et al.
Cancer Investigation
|
January 1, 1993
Combination treatment of acute myeloblastic leukemia with rhGM-CSF and standard induction chemotherapy
P Valent, C Sillaber, K Geissler, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 1, 1990
Prognostic significance of surface marker expression on blasts of patients with de novo acute myeloblastic leukemia
I Schwarzinger, P Valent, U Köller, et al.
British Journal of Haematology
|
March 1, 1985
Cell lineage heterogeneity in blast crisis of chronic myeloid leukaemia
P Bettelheim, D Lutz, O Majdic, et al.
The Journal of Clinical Investigation
|
June 1, 1985
Deficiency of the autologous mixed lymphocyte reaction in patients with classic hemophilia treated with commercial factor VIII concentrate. Correlation with T cell subset distribution, antibodies to lymphadenopathy-associated or human T lymphotropic virus, and analysis of the cellular basis of the deficiency
J S Smolen, P Bettelheim, U Köller, et al.
British Journal of Haematology
|
December 31, 1997
A hitherto unknown splice site defect in the protein S gene (PROS1): the mutation results in allelic exclusion and causes type I and type III protein S deficiency
S Mustafa, I Pabinger, K Vàradi, et al.
Page
of 48