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Pediatric Research|January 1, 1985
Age-related red cell enzymes in children with transient erythroblastopenia of childhood and with hemolytic anemiaE Beutler, G HartmanBlood|March 1, 1979
Erythrocyte cellular and membrane deformability in hereditary spherocytosisK Nakashima, E BeutlerClinical and Laboratory Haematology|January 1, 1980
A simplified method for studies of haemoglobin biosynthesisC Tegos, E BeutlerProceedings of the National Academy of Sciences of the United States of America|May 1, 1993
Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemiaL Baronciani, E BeutlerAmerican Journal of Human Genetics|December 1, 1990
The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and AsiaE Beutler, W KuhlBlood|May 29, 2000
Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white populationE Beutler, T GelbartThe Journal of Clinical Investigation|April 1, 1995
Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemiaL Baronciani, E BeutlerAmerican Journal of Clinical Pathology|December 1, 1981
Falsely normal value in fluorometric transferase screening of galactosemic blood. A cautionary noteE Beutler, T GelbartBlood|October 1, 1983
Phosphoglycolate phosphatase and 2,3-diphosphoglycerate in red cells of normal and anemic subjectsR Somoza, E BeutlerTransfusion|March 1, 1984
Measurement of the viability of stored red cells by the single-isotope technique using 51Cr. Analysis of validityE Beutler, C WestPageof 667