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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
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
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
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
Current Opinion in Pediatrics
|
February 15, 2001
Sickle cell disease: no longer a single gene disorder
D H Chui, G J Dover
Blood
|
December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects
G J Dover, S H Boyer
Blood
|
April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production
G J Dover, S H Boyer
Blood
|
July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate
G J Dover, S Brusilow, S Charache
Page
of 6
Search research articles
Search
Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 6
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
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
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
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
Current Opinion in Pediatrics
|
February 15, 2001
Sickle cell disease: no longer a single gene disorder
D H Chui, G J Dover
Blood
|
December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects
G J Dover, S H Boyer
Blood
|
April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production
G J Dover, S H Boyer
Blood
|
July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate
G J Dover, S Brusilow, S Charache
Page
of 6