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Obstetrics and Gynecology
|
April 1, 1980
Management of sickle cell disease in pregnant patients
S Charache, J Scott, J Niebyl, et al.
The Journal of Biological Chemistry
|
November 10, 1979
Conformation in solution of hemoglobin Osler (alpha 2 A beta 2 145 Tyr replaced by Asp)
E Bucci, C Fronticelli, J Nicklas, et al.
The American Journal of Medicine
|
May 1, 1983
Effects of blood transfusion on exercise capacity in patients with sickle-cell anemia
S Charache, E R Bleecker, D S Bross
The Johns Hopkins Medical Journal
|
March 1, 1977
Peripheral and optic neuritis in a patient with hemoglobin SC disease during treatment of salmonella osteomyelitis with chloramphenicol
S Charache, D Finkelstein, P S Lietman, et al.
Blood
|
March 1, 1976
Evaluation of extracorporeal alkylation of red cells as a potential treatment for sickle cell anemia
S Charache, R Dreyer, I Zimmerman, et al.
American Journal of Clinical Pathology
|
April 1, 1979
Comparison of microchromatography and electrophoresis with elution for hemoglobin A2 (Hb A2) quantitation
S R Hamilton, M E Miller, M Jessop, et al.
Blood
|
December 1, 1978
Variability of the homeostatic response to altered p50
S Charache, S Achuff, R Winslow, et al.
The New England Journal of Medicine
|
December 28, 1978
Individual variation in the production and survival of F cells in sickle-cell disease
G J Dover, S H Boyer, S Charache, et al.
FEBS Letters
|
May 11, 1970
Binding of 2,3-diphosphoglycerate to normal and abnormal oxyhemoglobin
D Diederich, A Diederich, J Carreras, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Progress toward increasing fetal hemoglobin production in man: experience with 5-azacytidine and hydroxyurea
G J Dover, S Charache, R Nora, et al.
Page
of 14
Search research articles
Search
Showing results (81-90 of 133) with videos related to
Sort By:
Page
of 14
Obstetrics and Gynecology
|
April 1, 1980
Management of sickle cell disease in pregnant patients
S Charache, J Scott, J Niebyl, et al.
The Journal of Biological Chemistry
|
November 10, 1979
Conformation in solution of hemoglobin Osler (alpha 2 A beta 2 145 Tyr replaced by Asp)
E Bucci, C Fronticelli, J Nicklas, et al.
The American Journal of Medicine
|
May 1, 1983
Effects of blood transfusion on exercise capacity in patients with sickle-cell anemia
S Charache, E R Bleecker, D S Bross
The Johns Hopkins Medical Journal
|
March 1, 1977
Peripheral and optic neuritis in a patient with hemoglobin SC disease during treatment of salmonella osteomyelitis with chloramphenicol
S Charache, D Finkelstein, P S Lietman, et al.
Blood
|
March 1, 1976
Evaluation of extracorporeal alkylation of red cells as a potential treatment for sickle cell anemia
S Charache, R Dreyer, I Zimmerman, et al.
American Journal of Clinical Pathology
|
April 1, 1979
Comparison of microchromatography and electrophoresis with elution for hemoglobin A2 (Hb A2) quantitation
S R Hamilton, M E Miller, M Jessop, et al.
Blood
|
December 1, 1978
Variability of the homeostatic response to altered p50
S Charache, S Achuff, R Winslow, et al.
The New England Journal of Medicine
|
December 28, 1978
Individual variation in the production and survival of F cells in sickle-cell disease
G J Dover, S H Boyer, S Charache, et al.
FEBS Letters
|
May 11, 1970
Binding of 2,3-diphosphoglycerate to normal and abnormal oxyhemoglobin
D Diederich, A Diederich, J Carreras, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Progress toward increasing fetal hemoglobin production in man: experience with 5-azacytidine and hydroxyurea
G J Dover, S Charache, R Nora, et al.
Page
of 14