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P R McCurdy

Showing results (31-40 of 53) with videos related to

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Biochimica Et Biophysica Acta|August 31, 1972
Identification of haemoglobin C GeorgetownA Lang, H Lehmann, P R McCurdy, et al.
Revue Europeenne D'Etudes Cliniques Et Biologiques. European Journal of Clinical and Biological Research|January 1, 1972
Red cell glucose-6-phosphate dehydrogenase variants in RumaniaP R McCurdy, J H Schneer, I M Hansen
Biochemistry|March 7, 1978
Proton nuclear magnetic resonance studies of hemoglobin Providence (beta82EF6 Lys replaced by Asn or Asp): a residue involved in anion bindingK J Wiechelman, J Fox, P R McCurdy, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1975
Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or CP R McCurdy, A S Sherman, H Kamuzora, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1973
Homozygous beta thalassemia in American Blacks: the problem of mild thalassemiaA S Braverman, P R McCurdy, O Manos, et al.
The American Journal of the Medical Sciences|October 1, 1972
The effect of oral urea administration on red cell survival in sickle cell diseaseT A Bensinger, L Mahmood, M E Conrad, et al.
The Journal of Laboratory and Clinical Medicine|September 1, 1973
Variants of glucose-6-phosphate dehydrogenase (G-6-PD) associated with G-6-PD deficiency in Puerto RicansP R McCurdy, N Maldonado, D E Dillon, et al.
American Journal of Clinical Pathology|February 1, 1988
Hemolysis in sickle cell disease as measured by endogenous carbon monoxide production. A preliminary reportD L Solanki, P R McCurdy, F F Cuttitta, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1970
Further studies on glucose-6-phosphate dehydrogenase deficiency in Chinese subjectsP R McCurdy, R Q Blackwell, D Todd, et al.
The New England Journal of Medicine|October 28, 1971
Effect of intravenous urea in invert sugar on heme catabolism in sickle-cell anemiaT A Bensinger, M J Maisels, L Mahmood, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Biochimica Et Biophysica Acta|August 31, 1972
Identification of haemoglobin C GeorgetownA Lang, H Lehmann, P R McCurdy, et al.
Revue Europeenne D'Etudes Cliniques Et Biologiques. European Journal of Clinical and Biological Research|January 1, 1972
Red cell glucose-6-phosphate dehydrogenase variants in RumaniaP R McCurdy, J H Schneer, I M Hansen
Biochemistry|March 7, 1978
Proton nuclear magnetic resonance studies of hemoglobin Providence (beta82EF6 Lys replaced by Asn or Asp): a residue involved in anion bindingK J Wiechelman, J Fox, P R McCurdy, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1975
Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or CP R McCurdy, A S Sherman, H Kamuzora, et al.
The Journal of Laboratory and Clinical Medicine|June 1, 1973
Homozygous beta thalassemia in American Blacks: the problem of mild thalassemiaA S Braverman, P R McCurdy, O Manos, et al.
The American Journal of the Medical Sciences|October 1, 1972
The effect of oral urea administration on red cell survival in sickle cell diseaseT A Bensinger, L Mahmood, M E Conrad, et al.
The Journal of Laboratory and Clinical Medicine|September 1, 1973
Variants of glucose-6-phosphate dehydrogenase (G-6-PD) associated with G-6-PD deficiency in Puerto RicansP R McCurdy, N Maldonado, D E Dillon, et al.
American Journal of Clinical Pathology|February 1, 1988
Hemolysis in sickle cell disease as measured by endogenous carbon monoxide production. A preliminary reportD L Solanki, P R McCurdy, F F Cuttitta, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1970
Further studies on glucose-6-phosphate dehydrogenase deficiency in Chinese subjectsP R McCurdy, R Q Blackwell, D Todd, et al.
The New England Journal of Medicine|October 28, 1971
Effect of intravenous urea in invert sugar on heme catabolism in sickle-cell anemiaT A Bensinger, M J Maisels, L Mahmood, et al.
Pageof 6