Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Charache

Showing results (91-100 of 133) with videos related to

Pageof 14
Sort By:
American Journal of Clinical Pathology|March 1, 1992
Accuracy and utility of differential white blood cell count in the neonatal intensive care unitS Charache, L Nelson, D Saw, et al.
Radiology|May 1, 1987
Abdominal pain in sickle cell disease: the role of CTD Magid, E K Fishman, S Charache, et al.
The Journal of Clinical Investigation|April 1, 1970
Effect of 2,3-diphosphoglycerate on oxygen affinity of blood in sickle cell anemiaS Charache, S Grisolia, A J Fiedler, et al.
Annals of the New York Academy of Sciences|January 1, 1974
Thalassemia in black americansS Charache, C L Conley, T D Doeblin, et al.
Biochemistry|November 24, 1970
Electron paramagnetic resonance studies of spin-labeled hemoglobins. II. Roles of subunit interactions and of intermediate structures in the cooperative oxygenation of hemoglobin and the results of hemoglobin Yakima, hemoglobin J capetown, and carboxypeptidases A and B treated hemoglobin AJ J Baldassare, S Charache, R T Jones, et al.
Mayo Clinic Proceedings|November 1, 1971
Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln)V F Fairbanks, J E Maldonado, S Charache, 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.
Archives of Internal Medicine|November 1, 1982
Aplastic crisis due to extensive bone marrow necrosis in sickle cell diseaseD M Pardoll, R J Rodeheffer, R R Smith, 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.
Biochemistry|April 25, 1972
Nuclear magnetic resonance studies of hemoglobins. VII. Tertiary structure around ligand binding site in carbonmonoxyhemoglobinT R Lindstrom, I B Norén, S Charache, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
American Journal of Clinical Pathology|March 1, 1992
Accuracy and utility of differential white blood cell count in the neonatal intensive care unitS Charache, L Nelson, D Saw, et al.
Radiology|May 1, 1987
Abdominal pain in sickle cell disease: the role of CTD Magid, E K Fishman, S Charache, et al.
The Journal of Clinical Investigation|April 1, 1970
Effect of 2,3-diphosphoglycerate on oxygen affinity of blood in sickle cell anemiaS Charache, S Grisolia, A J Fiedler, et al.
Annals of the New York Academy of Sciences|January 1, 1974
Thalassemia in black americansS Charache, C L Conley, T D Doeblin, et al.
Biochemistry|November 24, 1970
Electron paramagnetic resonance studies of spin-labeled hemoglobins. II. Roles of subunit interactions and of intermediate structures in the cooperative oxygenation of hemoglobin and the results of hemoglobin Yakima, hemoglobin J capetown, and carboxypeptidases A and B treated hemoglobin AJ J Baldassare, S Charache, R T Jones, et al.
Mayo Clinic Proceedings|November 1, 1971
Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln)V F Fairbanks, J E Maldonado, S Charache, 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.
Archives of Internal Medicine|November 1, 1982
Aplastic crisis due to extensive bone marrow necrosis in sickle cell diseaseD M Pardoll, R J Rodeheffer, R R Smith, 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.
Biochemistry|April 25, 1972
Nuclear magnetic resonance studies of hemoglobins. VII. Tertiary structure around ligand binding site in carbonmonoxyhemoglobinT R Lindstrom, I B Norén, S Charache, et al.
Pageof 14