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Molecular Genetics and Metabolism|August 5, 2000
Approach to gene therapy of glycogenosis type II (Pompe disease)L PoenaruAnnals of Medicine|April 20, 2001
From gene transfer to gene therapy in lysosomal storage diseases affecting the central nervous systemL PoenaruAnnales De Biologie Clinique|January 1, 1988
[Prenatal diagnosis of hereditary metabolic diseases in 1987]L PoenaruBiomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Molecular epidemiology of Tay-Sachs disease in EuropeL Poenaru, S AkliBiomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 29, 2000
Gene therapy in lysosomal diseasesC Caillaud, L PoenaruBiochemical and Biophysical Research Communications|April 20, 1999
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatchesD P Germain, L PoenaruPrenatal Diagnosis|April 1, 1983
Amniotic fluid protease activity and the prenatal detection of cystic fibrosisL Poenaru, M C VinetBiochimie|January 1, 1983
Purification of human liver uridylyl transferase and comparison with the erythrocyte enzymeJ Banroques, C Gregori, J C DreyfusActa Zoologica Et Pathologica Antverpiensia|August 1, 1977
[Human myopathy and animal muscular dystrophy]G Schapira, J C Dreyfus, F SchapiraPediatric Research|November 1, 1980
Phosphofructokinase in human fetusA Kahn, D Cottreau, J C DreyfusPageof 11