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G J Dover

Showing results (41-50 of 80) with videos related to

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The American Journal of Medicine|March 1, 1977
Hemoglobin SC, SS/GPhiladelphia and SOArab diseases diagnostic importance of an integrative analysis of clinical, hematologic and electrophoretic findingsS Charache, W H Zinkham, J D Dickerman, et al.
Progress in Clinical and Biological Research|January 1, 1989
Manipulation of HbF production with hematopoietic growth factorsK T McDonagh, G J Dover, R Donahue, et al.
Blood|February 15, 1995
An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and ageY C Chang, K D Smith, R D Moore, et al.
Blood|January 11, 1991
Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regionsE P Economou, S E Antonarakis, H H Kazazian, et al.
Urology|April 1, 1995
Evaluation of erectile function in men with sickle cell diseaseA L Burnett, R P Allen, C M Tempany, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1989
Philadelphia-chromosome positive essential thrombocythemia. Two cases in childrenM B Kastan, B A Zehnbauer, B G Leventhal, et al.
Journal of Pediatric Hematology/Oncology|December 18, 1998
The costs of children with sickle cell anemia: preparing for managed careJ H Bilenker, W E Weller, T J Shaffer, et al.
Seminars in Oncology|June 1, 1992
Hydroxyurea and erythropoietin therapy in sickle cell anemiaM A Goldberg, C Brugnara, G J Dover, et al.
Progress in Clinical and Biological Research|January 1, 1983
5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell diseaseG J Dover, S H Charache, S H Boyer, et al.
The New England Journal of Medicine|April 12, 1990
Hematologic responses of patients with sickle cell disease to treatment with hydroxyureaG P Rodgers, G J Dover, C T Noguchi, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
The American Journal of Medicine|March 1, 1977
Hemoglobin SC, SS/GPhiladelphia and SOArab diseases diagnostic importance of an integrative analysis of clinical, hematologic and electrophoretic findingsS Charache, W H Zinkham, J D Dickerman, et al.
Progress in Clinical and Biological Research|January 1, 1989
Manipulation of HbF production with hematopoietic growth factorsK T McDonagh, G J Dover, R Donahue, et al.
Blood|February 15, 1995
An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and ageY C Chang, K D Smith, R D Moore, et al.
Blood|January 11, 1991
Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regionsE P Economou, S E Antonarakis, H H Kazazian, et al.
Urology|April 1, 1995
Evaluation of erectile function in men with sickle cell diseaseA L Burnett, R P Allen, C M Tempany, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1989
Philadelphia-chromosome positive essential thrombocythemia. Two cases in childrenM B Kastan, B A Zehnbauer, B G Leventhal, et al.
Journal of Pediatric Hematology/Oncology|December 18, 1998
The costs of children with sickle cell anemia: preparing for managed careJ H Bilenker, W E Weller, T J Shaffer, et al.
Seminars in Oncology|June 1, 1992
Hydroxyurea and erythropoietin therapy in sickle cell anemiaM A Goldberg, C Brugnara, G J Dover, et al.
Progress in Clinical and Biological Research|January 1, 1983
5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell diseaseG J Dover, S H Charache, S H Boyer, et al.
The New England Journal of Medicine|April 12, 1990
Hematologic responses of patients with sickle cell disease to treatment with hydroxyureaG P Rodgers, G J Dover, C T Noguchi, et al.
Pageof 8