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Human Molecular Genetics|June 21, 2002
Muscle as a putative producer of acid alpha-glucosidase for glycogenosis type II gene therapyE Martin-Touaux, J P Puech, D Château, et al.Human Genetics|April 1, 1992
Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in PortugalC Caillaud, L Vilarinho, A Vilarinho, et al.Medicine and Science in Sports and Exercise|August 26, 1998
Exercise training reduces myocardial lipid peroxidation following short-term ischemia-reperfusionH A Demirel, S K Powers, C Caillaud, et al.Optics Express|June 13, 2014
Large-mode-area infrared guiding in ultrafast laser written waveguides in sulfur-based chalcogenide glassesC D'Amico, G Cheng, C Mauclair, et al.Human Genetics|December 1, 1988
Interstitial deletion of chromosome 15: two casesL D Formiga, L Poenaru, F Couronne, et al.Neurology|May 29, 2008
Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe diseaseP Laforêt, P Petiot, M Nicolino, et al.Journal of Inherited Metabolic Disease|July 25, 2008
Phenotypic spectrum of fucosidosis in TunisiaH Ben Turkia, N Tebib, H Azzouz, et al.Archives De L'Institut Pasteur De Tunis|April 25, 2009
[Mutation spectrum of Gaucher disease in Tunisia: high frequency of N370S/Rec NciI compound heterozygous]W Cherif, H Ben Turkia, N Tebib, et al.Pathologie-Biologie|May 1, 2012
[Molecular diagnosis of Gaucher disease in Tunisia]W Cherif, H Ben Turkia, F Ben Rhouma, et al.Acta Neuropathologica Communications|September 7, 2017
Long-term neurologic and cardiac correction by intrathecal gene therapy in Pompe diseaseJ Hordeaux, L Dubreil, C Robveille, et al.Pageof 14