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Blood|July 10, 1998
Six previously undescribed pyruvate kinase mutations causing enzyme deficiencyA Demina, K I Varughese, J Barbot, et al.Acta Haematologica|January 1, 1983
Coexistence of alpha-thalassemia and a new pyruvate kinase variant: PK FukienE Beutler, L FormanHematopathology and Molecular Hematology|June 3, 1998
Structure and linkage relationships of the region containing the human L-type pyruvate kinase (PKLR) and glucocerebrosidase (GBA) genesA Demina, E Boas, E BeutlerMolecular Medicine (Cambridge, Mass.)|November 1, 1994
Glucocerebrosidase mutations in Gaucher diseaseE Beutler, A Demina, T GelbartProceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?E Beutler, T Gelbart, A DeminaMedicine|March 1, 1988
Enzymatic diagnosis in non-spherocytic hemolytic anemiaA Hirono, L Forman, E BeutlerBlood|November 1, 1987
Effect of oxalate and malonate on red cell metabolismE Beutler, L Forman, C WestProceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Phosphatidylserine exposure and red cell viability in red cell aging and in hemolytic anemiaF E Boas, L Forman, E BeutlerThe American Journal of Medicine|November 1, 1987
Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency"E Beutler, L Forman, E Rios-LarrainPageof 91