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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2014
[Principles of therapeutic approaches for mucopolysaccharidoses]C CaillaudAnnals 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 PoenaruNeuroreport|May 9, 1994
In vivo transfer of a marker gene to study motoneuronal developmentF Lisovoski, J Cadusseau, S Akli, et al.Gene Therapy|September 10, 2003
Widespread distribution of beta-hexosaminidase activity in the brain of a Sandhoff mouse model after coinjection of adenoviral vector and mannitolC Bourgoin, C Emiliani, E J Kremer, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Molecular epidemiology of Tay-Sachs disease in EuropeL Poenaru, S AkliBiochemical 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 VinetBiochimica Et Biophysica Acta|January 12, 1979
Alpha-mannosidase in human red cellsL Poenaru, J C DreyfusAnnales De Biologie Clinique|January 1, 1975
[Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis]J C Dreyfus, L PoenaruPageof 14