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J-L Vives Corrons

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Human Genetics|January 1, 1982
Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favismJ L Vives Corrons, A Pujades
Annals of Hematology|October 24, 2001
Red cell membrane Na+ transport systems in hereditary spherocytosis: relevance to understanding the increased Na+ permeabilityJ L Vives Corrons, I Besson
Journal of Clinical Pathology|December 24, 2008
Neonatal haemoglobinopathy screening in SpainM Mañú Pereira, J-L Vives Corrons
Biochimica Et Biophysica Acta|November 21, 1991
Effect of TPA on fructose 2,6-bisphosphate levels and protein kinase C activity in B-chronic lymphocytic leukemia (B-CLL)D Colomer, J L Vives Corrons, R Bartrons
Human Genetics|April 5, 1979
Electrophoretic demonstration of heterozygosis in hereditary pyruvate kinase deficiency. An unusual methodA Kahn, J Marie, J L Vives-Corrons
Enzyme|January 1, 1988
Increase of enzyme activities following the in vitro peroxidation of normal human red blood cellsJ L Vives Corrons, M A Pujades, D Colomer
Human Genetics|December 15, 1976
Hereditary hemolytic anemia with erythrocyte pyrimidine 5'-nucleotidase deficiency in Spain. Clinical, biological and familial studiesJ L Vives-Corrons, E Montserrat-Costa, C Rozman
Hemoglobin|January 1, 1991
Erythrocyte fructose 2,6-bisphosphate content in congenital hemolytic anemiasD Colomer, A Pujades, E Carballo, et al.
Cancer Research|April 1, 1987
Control of phosphofructokinase by fructose 2,6-bisphosphate in B-lymphocytes and B-chronic lymphocytic leukemia cellsD Colomer, J L Vives-Corrons, A Pujades, et al.
Annals of Hematology|August 3, 2021
Concise review: how do red blood cells born, live, and die?J L Vives Corrons, L Berga Casafont, E Feliu Frasnedo
Pageof 12

Showing results (1-10 of 118) with videos related to

Sort By:
Pageof 12
Human Genetics|January 1, 1982
Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favismJ L Vives Corrons, A Pujades
Annals of Hematology|October 24, 2001
Red cell membrane Na+ transport systems in hereditary spherocytosis: relevance to understanding the increased Na+ permeabilityJ L Vives Corrons, I Besson
Journal of Clinical Pathology|December 24, 2008
Neonatal haemoglobinopathy screening in SpainM Mañú Pereira, J-L Vives Corrons
Biochimica Et Biophysica Acta|November 21, 1991
Effect of TPA on fructose 2,6-bisphosphate levels and protein kinase C activity in B-chronic lymphocytic leukemia (B-CLL)D Colomer, J L Vives Corrons, R Bartrons
Human Genetics|April 5, 1979
Electrophoretic demonstration of heterozygosis in hereditary pyruvate kinase deficiency. An unusual methodA Kahn, J Marie, J L Vives-Corrons
Enzyme|January 1, 1988
Increase of enzyme activities following the in vitro peroxidation of normal human red blood cellsJ L Vives Corrons, M A Pujades, D Colomer
Human Genetics|December 15, 1976
Hereditary hemolytic anemia with erythrocyte pyrimidine 5'-nucleotidase deficiency in Spain. Clinical, biological and familial studiesJ L Vives-Corrons, E Montserrat-Costa, C Rozman
Hemoglobin|January 1, 1991
Erythrocyte fructose 2,6-bisphosphate content in congenital hemolytic anemiasD Colomer, A Pujades, E Carballo, et al.
Cancer Research|April 1, 1987
Control of phosphofructokinase by fructose 2,6-bisphosphate in B-lymphocytes and B-chronic lymphocytic leukemia cellsD Colomer, J L Vives-Corrons, A Pujades, et al.
Annals of Hematology|August 3, 2021
Concise review: how do red blood cells born, live, and die?J L Vives Corrons, L Berga Casafont, E Feliu Frasnedo
Pageof 12