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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 diarrhoea
A Gomez-Brouchet, P Cintas, E Lagier, et al.
Annals of Neurology
|
January 1, 1994
Human beta-mannosidase deficiency associated with peripheral neuropathy
T Levade, D Graber, V Flurin, et al.
The British Journal of Dermatology
|
April 1, 1994
Neutral lipid storage disease. Case report and lipid studies
M 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 resistance
J 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 sisters
M 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 B
E 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 cells
F Malecaze, A Decha, B Serre, et al.
Human Gene Therapy
|
June 12, 1999
Retrovirus-mediated correction of the metabolic defect in cultured Farber disease cells
J 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 death
E Lafont, D Milhas, S Carpentier, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 124) with videos related to
Sort By:
Page
of 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 diarrhoea
A Gomez-Brouchet, P Cintas, E Lagier, et al.
Annals of Neurology
|
January 1, 1994
Human beta-mannosidase deficiency associated with peripheral neuropathy
T Levade, D Graber, V Flurin, et al.
The British Journal of Dermatology
|
April 1, 1994
Neutral lipid storage disease. Case report and lipid studies
M 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 resistance
J 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 sisters
M 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 B
E 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 cells
F Malecaze, A Decha, B Serre, et al.
Human Gene Therapy
|
June 12, 1999
Retrovirus-mediated correction of the metabolic defect in cultured Farber disease cells
J 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 death
E Lafont, D Milhas, S Carpentier, et al.
Page
of 13