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M T Vanier

Showing results (91-100 of 156) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 10, 2005
[X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences]G Lesca, M T Vanier, E Creisson, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rateW Sperl, G Bart, M T Vanier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2006
Niemann-Pick type C disease in a 68-year-old patientG Trendelenburg, M T Vanier, S Maza, et al.
Lancet (London, England)|May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cellsM T Vanier, R M Rousson, G Mandon, et al.
Clinical Genetics|January 1, 1985
Biochemical studies in Niemann-Pick disease. III. In vitro and in vivo assays of sphingomyelin degradation in cultured skin fibroblasts and amniotic fluid cells for the diagnosis of the various forms of the diseaseM T Vanier, R Rousson, I Garcia, et al.
Neuroscience Letters|April 29, 1983
Effect of tricyclic antidepressants on sphingomyelinase and other sphingolipid hydrolases in C6 cultured glioma cellsS Albouz, M T Vanier, J J Hauw, et al.
Pediatrie|September 1, 1977
[Krabbe's disease]L Larget-Piet, M T Vanier, J Berthelot, et al.
Clinical Genetics|May 1, 1988
Niemann-Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification. A collaborative study on 70 patientsM T Vanier, D A Wenger, M E Comly, et al.
Journal of Neuroscience Research|January 29, 2000
Biochemistry and neuropathology of mice doubly deficient in synthesis and degradation of galactosylceramideT Ezoe, M T Vanier, Y Oya, et al.
Journal of Neuroscience Research|January 29, 2000
Twitcher mice with only a single active galactosylceramide synthase gene exhibit clearly detectable but therapeutically minor phenotypic improvementsT Ezoe, M T Vanier, Y Oya, et al.
Pageof 16

Showing results (91-100 of 156) with videos related to

Sort By:
Pageof 16
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 10, 2005
[X-linked adrenoleukodystrophy in a female proband: clinical presentation, biological diagnosis and family consequences]G Lesca, M T Vanier, E Creisson, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rateW Sperl, G Bart, M T Vanier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2006
Niemann-Pick type C disease in a 68-year-old patientG Trendelenburg, M T Vanier, S Maza, et al.
Lancet (London, England)|May 6, 1989
Diagnosis of Niemann-Pick disease type C on chorionic villus cellsM T Vanier, R M Rousson, G Mandon, et al.
Clinical Genetics|January 1, 1985
Biochemical studies in Niemann-Pick disease. III. In vitro and in vivo assays of sphingomyelin degradation in cultured skin fibroblasts and amniotic fluid cells for the diagnosis of the various forms of the diseaseM T Vanier, R Rousson, I Garcia, et al.
Neuroscience Letters|April 29, 1983
Effect of tricyclic antidepressants on sphingomyelinase and other sphingolipid hydrolases in C6 cultured glioma cellsS Albouz, M T Vanier, J J Hauw, et al.
Pediatrie|September 1, 1977
[Krabbe's disease]L Larget-Piet, M T Vanier, J Berthelot, et al.
Clinical Genetics|May 1, 1988
Niemann-Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification. A collaborative study on 70 patientsM T Vanier, D A Wenger, M E Comly, et al.
Journal of Neuroscience Research|January 29, 2000
Biochemistry and neuropathology of mice doubly deficient in synthesis and degradation of galactosylceramideT Ezoe, M T Vanier, Y Oya, et al.
Journal of Neuroscience Research|January 29, 2000
Twitcher mice with only a single active galactosylceramide synthase gene exhibit clearly detectable but therapeutically minor phenotypic improvementsT Ezoe, M T Vanier, Y Oya, et al.
Pageof 16