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Maryland Medical Journal (Baltimore, Md. : 1985)
|
April 1, 1990
Management of sickle cell anemia in children
G J Dover
Annals of the New York Academy of Sciences
|
July 21, 1998
Hemoglobin switching protocols in thalassemia. Experience with sodium phenylbutyrate and hydroxyurea
G J Dover
Annals of the New York Academy of Sciences
|
January 1, 1990
Pharmacologic manipulation of fetal hemoglobin. Update on clinical trials with hydroxyurea
G J Dover
Annals of Neurology
|
March 11, 1999
A new look at neuropathology in sickle cell disease
G J Dover
The Journal of Clinical Investigation
|
November 1, 1980
Cellular mechanisms for increased fetal hemoglobin production in culture. Evidence for continuous commitment to fetal hemoglobin production during burst formation
G J Dover, M Ogawa
Progress in Clinical and Biological Research
|
January 1, 1989
Stimulation of fetal hemoglobin production by hydroxyurea in sickle cell anemia
G J Dover, S Charache
American Journal of Hematology
|
June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis X
C Sheils, G J Dover
Seminars in Oncology
|
June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell disease
G J Dover, S Charache
Annals of the New York Academy of Sciences
|
January 1, 1989
Chemotherapy and hemoglobin F synthesis in sickle cell disease
G J Dover, S Charache
Progress in Clinical and Biological Research
|
January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trials
G J Dover, S Charache
Page
of 8
Search research articles
Search
Showing results (1-10 of 80) with videos related to
Sort By:
Page
of 8
Maryland Medical Journal (Baltimore, Md. : 1985)
|
April 1, 1990
Management of sickle cell anemia in children
G J Dover
Annals of the New York Academy of Sciences
|
July 21, 1998
Hemoglobin switching protocols in thalassemia. Experience with sodium phenylbutyrate and hydroxyurea
G J Dover
Annals of the New York Academy of Sciences
|
January 1, 1990
Pharmacologic manipulation of fetal hemoglobin. Update on clinical trials with hydroxyurea
G J Dover
Annals of Neurology
|
March 11, 1999
A new look at neuropathology in sickle cell disease
G J Dover
The Journal of Clinical Investigation
|
November 1, 1980
Cellular mechanisms for increased fetal hemoglobin production in culture. Evidence for continuous commitment to fetal hemoglobin production during burst formation
G J Dover, M Ogawa
Progress in Clinical and Biological Research
|
January 1, 1989
Stimulation of fetal hemoglobin production by hydroxyurea in sickle cell anemia
G J Dover, S Charache
American Journal of Hematology
|
June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis X
C Sheils, G J Dover
Seminars in Oncology
|
June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell disease
G J Dover, S Charache
Annals of the New York Academy of Sciences
|
January 1, 1989
Chemotherapy and hemoglobin F synthesis in sickle cell disease
G J Dover, S Charache
Progress in Clinical and Biological Research
|
January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trials
G J Dover, S Charache
Page
of 8