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L Poenaru

Showing results (51-60 of 92) with videos related to

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Prenatal Diagnosis|October 1, 1982
Prenatal diagnosis of a heterozygote for mucopolysaccharidosis type VII (beta-glucuronidase deficiency)L Poenaru, L Castelnau, J Mossman, et al.
American Journal of Human Genetics|May 1, 1977
Characterization of a variant of beta-hexosaminidase: "hexosaminidase Paris"J C Dreyfus, L Poenaru, M Vibert, et al.
Clinical Genetics|May 1, 1985
Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsyA M Besançon, L Castelnau, H Nicolesco, et al.
Genomics|September 1, 1991
Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragmentsS Akli, J Chelly, J M Lacorte, et al.
Annales De Medecine Interne|January 1, 1985
[Early prenatal diagnosis of lysosomal enzymopathies from biopsies of trophoblasts]L Poenaru, J P Belon, A M Besançon, et al.
Human Genetics|December 1, 1996
Fluorescence-assisted mismatch analysis (FAMA) for exhaustive screening of the alpha-galactosidase A gene and detection of carriers in Fabry diseaseD Germain, M Biasotto, M Tosi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1984
Sodium taurocholate effect on beta-glucosidase activity: a new approach for identification of Gaucher disease using the synthetic substrate and leucocytesJ Magalhães, M C Sá Miranda, R Pinto, et al.
Annales De Biologie Clinique|January 1, 1978
[Rational basis for a choice of enzymes in physiopathology (proceedings)]J C Dreyfus, F Schapira, J C Kaplan, et al.
Gene Therapy|August 1, 1995
Gene delivery into the central nervous system by nasal instillation in ratsR Draghia, C Caillaud, R Manicom, et al.
Biochemical and Biophysical Research Communications|March 30, 1984
High frequency of beta-hexosaminidase deficiency in lymphoblastoid cell linesJ C Dreyfus, J P Belon, S Gautron, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|October 1, 1982
Prenatal diagnosis of a heterozygote for mucopolysaccharidosis type VII (beta-glucuronidase deficiency)L Poenaru, L Castelnau, J Mossman, et al.
American Journal of Human Genetics|May 1, 1977
Characterization of a variant of beta-hexosaminidase: "hexosaminidase Paris"J C Dreyfus, L Poenaru, M Vibert, et al.
Clinical Genetics|May 1, 1985
Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsyA M Besançon, L Castelnau, H Nicolesco, et al.
Genomics|September 1, 1991
Seven novel Tay-Sachs mutations detected by chemical mismatch cleavage of PCR-amplified cDNA fragmentsS Akli, J Chelly, J M Lacorte, et al.
Annales De Medecine Interne|January 1, 1985
[Early prenatal diagnosis of lysosomal enzymopathies from biopsies of trophoblasts]L Poenaru, J P Belon, A M Besançon, et al.
Human Genetics|December 1, 1996
Fluorescence-assisted mismatch analysis (FAMA) for exhaustive screening of the alpha-galactosidase A gene and detection of carriers in Fabry diseaseD Germain, M Biasotto, M Tosi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1984
Sodium taurocholate effect on beta-glucosidase activity: a new approach for identification of Gaucher disease using the synthetic substrate and leucocytesJ Magalhães, M C Sá Miranda, R Pinto, et al.
Annales De Biologie Clinique|January 1, 1978
[Rational basis for a choice of enzymes in physiopathology (proceedings)]J C Dreyfus, F Schapira, J C Kaplan, et al.
Gene Therapy|August 1, 1995
Gene delivery into the central nervous system by nasal instillation in ratsR Draghia, C Caillaud, R Manicom, et al.
Biochemical and Biophysical Research Communications|March 30, 1984
High frequency of beta-hexosaminidase deficiency in lymphoblastoid cell linesJ C Dreyfus, J P Belon, S Gautron, et al.
Pageof 10