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Blood Cells, Molecules & Diseases
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September 23, 2000
Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity
G Papanikolaou, M Politou, E Terpos, et al.
American Journal of Hematology
|
June 28, 2001
Behcet's disease in a patient with chronic myelogenous leukemia under hydroxyurea treatment: a case report and review of the literature
G Vaiopoulos, E Terpos, N Viniou, et al.
Panminerva Medica
|
February 24, 2001
Micrococcus luteus: a putative cause of hepatic abscess?
T Andreopoulos, G Papanikolaou, M Politou, et al.
Acta Psychologica
|
March 1, 1993
A model for reaching control
D A Rosenbaum, S E Engelbrecht, M M Bushe, et al.
Leukemia & Lymphoma
|
July 1, 1995
Correlation of the site of M-bcr breakpoint with chronic phase duration, blastic crisis lineage and thrombocytosis in Ph1-positive chronic myelogenous leukemia
N A Viniou, M Matzourani, X Yataganas, et al.
Journal of Motor Behavior
|
December 29, 2009
Finding final postures
J Vaughan, D A Rosenbaum, C J Harp, et al.
Human Genetics
|
August 14, 1998
The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion events
G P Patrinos, P Kollia, A Loutradi-Anagnostou, et al.
Acta Haematologica
|
January 1, 1993
Flow-cytometric analysis of reticulocytes in normal cord blood
G S Paterakis, L Lykopoulou, J Papassotiriou, et al.
British Journal of Haematology
|
May 8, 1999
Molecular analysis of bcl-1/IgH junctional sequences in mantle cell lymphoma: potential mechanism of the t(11;14) chromosomal translocation
K Stamatopoulos, C Kosmas, C Belessi, et al.
Panminerva Medica
|
July 13, 2001
Clinical significance of the molecular detection of melanoma cells circulating in the peripheral blood in melanoma patients
K Konstantopoulos, M Psatha, V Kalotychou, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 105) with videos related to
Sort By:
Page
of 11
Blood Cells, Molecules & Diseases
|
September 23, 2000
Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity
G Papanikolaou, M Politou, E Terpos, et al.
American Journal of Hematology
|
June 28, 2001
Behcet's disease in a patient with chronic myelogenous leukemia under hydroxyurea treatment: a case report and review of the literature
G Vaiopoulos, E Terpos, N Viniou, et al.
Panminerva Medica
|
February 24, 2001
Micrococcus luteus: a putative cause of hepatic abscess?
T Andreopoulos, G Papanikolaou, M Politou, et al.
Acta Psychologica
|
March 1, 1993
A model for reaching control
D A Rosenbaum, S E Engelbrecht, M M Bushe, et al.
Leukemia & Lymphoma
|
July 1, 1995
Correlation of the site of M-bcr breakpoint with chronic phase duration, blastic crisis lineage and thrombocytosis in Ph1-positive chronic myelogenous leukemia
N A Viniou, M Matzourani, X Yataganas, et al.
Journal of Motor Behavior
|
December 29, 2009
Finding final postures
J Vaughan, D A Rosenbaum, C J Harp, et al.
Human Genetics
|
August 14, 1998
The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion events
G P Patrinos, P Kollia, A Loutradi-Anagnostou, et al.
Acta Haematologica
|
January 1, 1993
Flow-cytometric analysis of reticulocytes in normal cord blood
G S Paterakis, L Lykopoulou, J Papassotiriou, et al.
British Journal of Haematology
|
May 8, 1999
Molecular analysis of bcl-1/IgH junctional sequences in mantle cell lymphoma: potential mechanism of the t(11;14) chromosomal translocation
K Stamatopoulos, C Kosmas, C Belessi, et al.
Panminerva Medica
|
July 13, 2001
Clinical significance of the molecular detection of melanoma cells circulating in the peripheral blood in melanoma patients
K Konstantopoulos, M Psatha, V Kalotychou, et al.
Page
of 11