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British Journal of Cancer
|
April 4, 2013
Putative tumour suppressor gene necdin is hypermethylated and mutated in human cancer
L E De Faveri, C D Hurst, F M Platt, et al.
Journal of Inherited Metabolic Disease
|
December 27, 2006
Severe endothelial dysfunction in the aorta of a mouse model of Fabry disease; partial prevention by N-butyldeoxynojirimycin treatment
T Heare, N J Alp, D A Priestman, et al.
Brain : a Journal of Neurology
|
March 5, 2003
Central nervous system inflammation is a hallmark of pathogenesis in mouse models of GM1 and GM2 gangliosidosis
M Jeyakumar, R Thomas, E Elliot-Smith, et al.
NMR in Biomedicine
|
October 6, 2005
MRS reveals additional hexose N-acetyl resonances in the brain of a mouse model for Sandhoff disease
J P Lowe, D J Stuckey, F R Awan, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Sustained therapeutic effects of oral miglustat (Zavesca, N-butyldeoxynojirimycin, OGT 918) in type I Gaucher disease
D Elstein, C Hollak, J M F G Aerts, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2001
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy
F M Platt, M Jeyakumar, U Andersson, et al.
Trials
|
January 23, 2021
A master protocol to investigate a novel therapy acetyl-L-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia
T Fields, M Patterson, T Bremova-Ertl, et al.
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of 5
Search research articles
Search
Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 47 results.
British Journal of Cancer
|
April 4, 2013
Putative tumour suppressor gene necdin is hypermethylated and mutated in human cancer
L E De Faveri, C D Hurst, F M Platt, et al.
Journal of Inherited Metabolic Disease
|
December 27, 2006
Severe endothelial dysfunction in the aorta of a mouse model of Fabry disease; partial prevention by N-butyldeoxynojirimycin treatment
T Heare, N J Alp, D A Priestman, et al.
Brain : a Journal of Neurology
|
March 5, 2003
Central nervous system inflammation is a hallmark of pathogenesis in mouse models of GM1 and GM2 gangliosidosis
M Jeyakumar, R Thomas, E Elliot-Smith, et al.
NMR in Biomedicine
|
October 6, 2005
MRS reveals additional hexose N-acetyl resonances in the brain of a mouse model for Sandhoff disease
J P Lowe, D J Stuckey, F R Awan, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Sustained therapeutic effects of oral miglustat (Zavesca, N-butyldeoxynojirimycin, OGT 918) in type I Gaucher disease
D Elstein, C Hollak, J M F G Aerts, et al.
Journal of Inherited Metabolic Disease
|
June 19, 2001
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy
F M Platt, M Jeyakumar, U Andersson, et al.
Trials
|
January 23, 2021
A master protocol to investigate a novel therapy acetyl-L-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia
T Fields, M Patterson, T Bremova-Ertl, et al.
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of 5