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L Poenaru

Showing results (11-20 of 92) with videos related to

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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 29, 2000
Gene therapy in lysosomal diseasesC Caillaud, L Poenaru
Biochemical 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 Poenaru
Prenatal Diagnosis|April 1, 1983
Amniotic fluid protease activity and the prenatal detection of cystic fibrosisL Poenaru, M C Vinet
Lancet (London, England)|June 16, 1979
Prenatal diagnosis of Tay-Sachs diseaseJ C Dreyfus, L Poenaru
Biochimica Et Biophysica Acta|January 12, 1979
Alpha-mannosidase in human red cellsL Poenaru, J C Dreyfus
Clinical Biochemistry|December 1, 1979
White blood cells in the diagnosis of glycogenosis type IIL Poenaru, J C Dreyfus
Biochimica Et Biophysica Acta|March 23, 1973
Electrophoretic heterogeneity of human -mannosidaseL Poenaru, J C Dreyfus
Annales De Biologie Clinique|January 1, 1975
[Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis]J C Dreyfus, L Poenaru
Pediatric Research|April 1, 1980
White blood cells and the diagnosis of alpha-glucosidase deficiencyJ C Dreyfus, L Poenaru
Lancet (London, England)|January 29, 1977
Enzyme activity in fucosidosisJ C Dreyfus, L Poenaru
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|December 29, 2000
Gene therapy in lysosomal diseasesC Caillaud, L Poenaru
Biochemical 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 Poenaru
Prenatal Diagnosis|April 1, 1983
Amniotic fluid protease activity and the prenatal detection of cystic fibrosisL Poenaru, M C Vinet
Lancet (London, England)|June 16, 1979
Prenatal diagnosis of Tay-Sachs diseaseJ C Dreyfus, L Poenaru
Biochimica Et Biophysica Acta|January 12, 1979
Alpha-mannosidase in human red cellsL Poenaru, J C Dreyfus
Clinical Biochemistry|December 1, 1979
White blood cells in the diagnosis of glycogenosis type IIL Poenaru, J C Dreyfus
Biochimica Et Biophysica Acta|March 23, 1973
Electrophoretic heterogeneity of human -mannosidaseL Poenaru, J C Dreyfus
Annales De Biologie Clinique|January 1, 1975
[Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis]J C Dreyfus, L Poenaru
Pediatric Research|April 1, 1980
White blood cells and the diagnosis of alpha-glucosidase deficiencyJ C Dreyfus, L Poenaru
Lancet (London, England)|January 29, 1977
Enzyme activity in fucosidosisJ C Dreyfus, L Poenaru
Pageof 10