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Neurology|November 1, 1994
Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiencyC Antozzi, B Garavaglia, M Mora, et al.American Journal of Human Genetics|February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)M Zeviani, P Amati, N Bresolin, et al.Acta Neuropathologica. Supplementum|January 1, 1981
Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical studyF Cornelio, D Peluchetti, M Rimoldi, et al.Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.Annals of Neurology|May 1, 1989
Normalization of short-chain acylcoenzyme A dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme A dehydrogenase-deficient myopathyS DiDonato, C Gellera, D Peluchetti, et al.Neurology|March 1, 1990
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymesC Gellera, G Uziel, M Rimoldi, et al.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.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.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.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 5