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T Levade

Showing results (101-110 of 124) with videos related to

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Revue Neurologique|April 4, 2007
[Adult leukoencephalopathy caused by alpha-mannosidosis deficiency]G Castelnovo, T Levade, H M F Riise Stensland, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Adult Sandhoff disease presenting with chronic diarrhoeaA Gomez-Brouchet, P Cintas, E Lagier, et al.
Annals of Neurology|January 1, 1994
Human beta-mannosidase deficiency associated with peripheral neuropathyT Levade, D Graber, V Flurin, et al.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Biochimica Et Biophysica Acta|April 6, 1995
Inhibition of lysosomal acid sphingomyelinase by agents which reverse multidrug resistanceJ P Jaffrézou, Kevin Gang Chen, G E Durán, et al.
Dermatology (Basel, Switzerland)|January 1, 1993
Fabry's disease: heterozygous form of different expression in two monozygous twin sistersM C Marguery, F Giordano, M Parant, et al.
Human Genetics|August 21, 2001
Mutation analyses in 17 patients with deficiency in acid beta-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type BE Paschke, I Milos, H Kreimer-Erlacher, et al.
Gene Therapy|October 28, 2005
Prevention of posterior capsule opacification by the induction of therapeutic apoptosis of residual lens cellsF Malecaze, A Decha, B Serre, et al.
Human Gene Therapy|June 12, 1999
Retrovirus-mediated correction of the metabolic defect in cultured Farber disease cellsJ A Medin, T Takenaka, S Carpentier, et al.
Cell Death and Differentiation|September 26, 2009
Caspase-mediated inhibition of sphingomyelin synthesis is involved in FasL-triggered cell deathE Lafont, D Milhas, S Carpentier, et al.
Pageof 13

Showing results (101-110 of 124) with videos related to

Sort By:
Pageof 13
Revue Neurologique|April 4, 2007
[Adult leukoencephalopathy caused by alpha-mannosidosis deficiency]G Castelnovo, T Levade, H M F Riise Stensland, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Adult Sandhoff disease presenting with chronic diarrhoeaA Gomez-Brouchet, P Cintas, E Lagier, et al.
Annals of Neurology|January 1, 1994
Human beta-mannosidase deficiency associated with peripheral neuropathyT Levade, D Graber, V Flurin, et al.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Biochimica Et Biophysica Acta|April 6, 1995
Inhibition of lysosomal acid sphingomyelinase by agents which reverse multidrug resistanceJ P Jaffrézou, Kevin Gang Chen, G E Durán, et al.
Dermatology (Basel, Switzerland)|January 1, 1993
Fabry's disease: heterozygous form of different expression in two monozygous twin sistersM C Marguery, F Giordano, M Parant, et al.
Human Genetics|August 21, 2001
Mutation analyses in 17 patients with deficiency in acid beta-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type BE Paschke, I Milos, H Kreimer-Erlacher, et al.
Gene Therapy|October 28, 2005
Prevention of posterior capsule opacification by the induction of therapeutic apoptosis of residual lens cellsF Malecaze, A Decha, B Serre, et al.
Human Gene Therapy|June 12, 1999
Retrovirus-mediated correction of the metabolic defect in cultured Farber disease cellsJ A Medin, T Takenaka, S Carpentier, et al.
Cell Death and Differentiation|September 26, 2009
Caspase-mediated inhibition of sphingomyelin synthesis is involved in FasL-triggered cell deathE Lafont, D Milhas, S Carpentier, et al.
Pageof 13