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Pathobiology Annual
|
January 1, 1981
Pathogenesis of sickle cell disease
J W Eaton, R P Hebbel
The American Journal of Physiology
|
November 1, 1986
Ethane production as a measure of lipid peroxidation after renal ischemia
M S Paller, R P Hebbel
The Journal of Laboratory and Clinical Medicine
|
April 1, 1996
CD36-positive stress reticulocytosis in sickle cell anemia
P V Browne, R P Hebbel
The Journal of Clinical Investigation
|
August 10, 2000
Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice
D K Kaul, R P Hebbel
American Journal of Hematology
|
June 1, 1983
Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity
M H Steinberg, R P Hebbel
Blood
|
September 1, 1984
Phagocytosis of sickle erythrocytes: immunologic and oxidative determinants of hemolytic anemia
R P Hebbel, W J Miller
Seminars in Hematology
|
April 1, 1989
Pathobiology of heme interaction with the erythrocyte membrane
R P Hebbel, J W Eaton
The Journal of Laboratory and Clinical Medicine
|
March 1, 1997
The endothelial biology of sickle cell disease
R P Hebbel, G M Vercellotti
American Journal of Hematology
|
December 1, 1988
Unique promotion of erythrophagocytosis by malondialdehyde
R P Hebbel, W J Miller
Blood
|
October 1, 1988
Nonheme iron in sickle erythrocyte membranes: association with phospholipids and potential role in lipid peroxidation
S A Kuross, R P Hebbel
Page
of 12
Search research articles
Search
Showing results (21-30 of 116) with videos related to
Sort By:
Page
of 12
Pathobiology Annual
|
January 1, 1981
Pathogenesis of sickle cell disease
J W Eaton, R P Hebbel
The American Journal of Physiology
|
November 1, 1986
Ethane production as a measure of lipid peroxidation after renal ischemia
M S Paller, R P Hebbel
The Journal of Laboratory and Clinical Medicine
|
April 1, 1996
CD36-positive stress reticulocytosis in sickle cell anemia
P V Browne, R P Hebbel
The Journal of Clinical Investigation
|
August 10, 2000
Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice
D K Kaul, R P Hebbel
American Journal of Hematology
|
June 1, 1983
Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity
M H Steinberg, R P Hebbel
Blood
|
September 1, 1984
Phagocytosis of sickle erythrocytes: immunologic and oxidative determinants of hemolytic anemia
R P Hebbel, W J Miller
Seminars in Hematology
|
April 1, 1989
Pathobiology of heme interaction with the erythrocyte membrane
R P Hebbel, J W Eaton
The Journal of Laboratory and Clinical Medicine
|
March 1, 1997
The endothelial biology of sickle cell disease
R P Hebbel, G M Vercellotti
American Journal of Hematology
|
December 1, 1988
Unique promotion of erythrophagocytosis by malondialdehyde
R P Hebbel, W J Miller
Blood
|
October 1, 1988
Nonheme iron in sickle erythrocyte membranes: association with phospholipids and potential role in lipid peroxidation
S A Kuross, R P Hebbel
Page
of 12