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G J Dover

Showing results (31-40 of 80) with videos related to

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The New England Journal of Medicine|December 28, 1978
Individual variation in the production and survival of F cells in sickle-cell diseaseG J Dover, S H Boyer, S Charache, et al.
Blood|April 15, 1990
Serum-free culture of enriched hematopoietic progenitors reflects physiologic levels of fetal hemoglobin biosynthesisY Fujimori, M Ogawa, S C Clark, 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 hydroxyureaG J Dover, S Charache, R Nora, et al.
Journal of Molecular Evolution|April 1, 1992
The evolution of two west African populationsO C Stine, G J Dover, D Zhu, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1982
Lung abscess in sickle cell diseaseR J Leggiadro, G J Dover, M L Morse, et al.
Blood|January 1, 1987
Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemiaS Charache, G J Dover, M A Moyer, et al.
Pediatrics|June 2, 2000
Screening for iron deficiency anemia by dietary history in a high-risk populationD L Bogen, A K Duggan, G J Dover, et al.
Blood|September 1, 1985
5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimensG J Dover, S Charache, S H Boyer, et al.
British Journal of Haematology|May 8, 1999
Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyureaS K Ballas, M J Marcolina, G J Dover, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|December 1, 1976
Delineation of peripheral bone infarcts in a child with a rare hemoglobinopathy (SOArab) and purpura fulminans: case reportW C Klingensmith, E H Danish, G J Dover, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
The New England Journal of Medicine|December 28, 1978
Individual variation in the production and survival of F cells in sickle-cell diseaseG J Dover, S H Boyer, S Charache, et al.
Blood|April 15, 1990
Serum-free culture of enriched hematopoietic progenitors reflects physiologic levels of fetal hemoglobin biosynthesisY Fujimori, M Ogawa, S C Clark, 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 hydroxyureaG J Dover, S Charache, R Nora, et al.
Journal of Molecular Evolution|April 1, 1992
The evolution of two west African populationsO C Stine, G J Dover, D Zhu, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1982
Lung abscess in sickle cell diseaseR J Leggiadro, G J Dover, M L Morse, et al.
Blood|January 1, 1987
Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemiaS Charache, G J Dover, M A Moyer, et al.
Pediatrics|June 2, 2000
Screening for iron deficiency anemia by dietary history in a high-risk populationD L Bogen, A K Duggan, G J Dover, et al.
Blood|September 1, 1985
5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimensG J Dover, S Charache, S H Boyer, et al.
British Journal of Haematology|May 8, 1999
Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyureaS K Ballas, M J Marcolina, G J Dover, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|December 1, 1976
Delineation of peripheral bone infarcts in a child with a rare hemoglobinopathy (SOArab) and purpura fulminans: case reportW C Klingensmith, E H Danish, G J Dover, et al.
Pageof 8