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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1994
The principles of gene therapy in Duchenne muscular dystrophyG Karpati, G AcsadiAnnals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.Current Opinion in Molecular Therapeutics|March 16, 2001
Molecular therapy for glioblastomaG Karpati, H Li, J NalbantogluThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979
The effects of partial chronic denervation on forearm metabolismG Karpati, G Klassen, P TanserBrain : a Journal of Neurology|October 1, 1989
Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic studyS F Berkovic, S Carpenter, A Evans, et al.American Journal of Human Genetics|December 1, 1992
Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)L Boulet, G Karpati, E A ShoubridgeHuman Molecular Genetics|March 21, 1998
Complete restoration of a wild-type mtDNA genotype in regenerating muscle fibres in a patient with a tRNA point mutation and mitochondrial encephalomyopathyE A Shoubridge, T Johns, G KarpatiTrends in Neurosciences|February 1, 1996
The principles of gene therapy for the nervous systemG Karpati, H Lochmüller, J Nalbantoglu, et al.Cell|July 13, 1990
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial diseaseE A Shoubridge, G Karpati, K E HastingsJournal of Neuropathology and Experimental Neurology|April 10, 1999
Discordant expression of utrophin and its transcript in human and mouse skeletal musclesA O Gramolini, G Karpati, B J JasminPageof 90