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Journal of Neurology|August 1, 1995
Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathyG M Fabrizi, V Tiranti, C Mariotti, et al.FEBS Letters|May 6, 1991
Evidence that nebulin is a protein-ruler in muscle thin filamentsS Labeit, T Gibson, A Lakey, et al.Lancet (London, England)|July 20, 1991
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR)M Zeviani, C Gellera, C Antozzi, et al.Neurology|September 1, 2006
POLG1 in idiopathic Parkinson diseaseW Tiangyou, G Hudson, D Ghezzi, et al.European Journal of Human Genetics : EJHG|January 1, 1993
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) geneM Zeviani, F Muntoni, N Savarese, et al.American Journal of Medical Genetics|December 1, 1986
Metabolic myopathiesS DiMauro, A F Miranda, S Sakoda, et al.Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.Journal of Bioenergetics and Biomembranes|June 1, 1988
Molecular defects in cytochrome oxidase in mitochondrial diseasesS DiMauro, M Zeviani, R Rizzuto, et al.Biochemical and Biophysical Research Communications|May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patientF M Santorelli, E Bertini, V Petruzzella, et al.Journal of Neurology|September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic studyC Mariotti, G Uziel, F Carrara, et al.Pageof 18