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Journal of the Neurological Sciences|September 1, 1991
Riboflavin responsive multiple acyl-CoA dehydrogenase deficiency: functional evaluation of recovery after high dose vitamin supplementationD Peluchetti, C Antozzi, S Roi, et al.Annals of Neurology|November 1, 1978
Muscle carnitine palmityltransferase deficiency: a case with enzyme deficiency in cultured fibroblastsS DiDonato, F Cornelio, L Pacini, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1980
Friedreich's ataxia in northern Italy: I. Clinical, neurophysiological and in vivo biochemical studiesA D'Angelo, S DiDonato, G Negri, et al.Nature|May 25, 1989
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionM Zeviani, S Servidei, C Gellera, et al.European Journal of Biochemistry|May 20, 1990
Purification and properties of carnitine acetyltransferase from human liverW Bloisi, I Colombo, B Garavaglia, et al.Italian Journal of Neurological Sciences|February 1, 1986
Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophyG Uziel, F Cornelio, C Gellera, et al.Biochimica Et Biophysica Acta|September 13, 1994
Identification of 5' regulatory regions of the human carnitine palmitoyltransferase II geneL Montermini, H Wang, E Verderio, et al.The Journal of Clinical Investigation|March 1, 1994
Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathyC Mariotti, V Tiranti, F Carrara, et al.Nature Genetics|July 1, 1993
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patientsF Taroni, E Verderio, F Dworzak, et al.European Journal of Biochemistry|May 1, 1993
cDNA cloning and mitochondrial import of the beta-subunit of the human electron-transfer flavoproteinG Finocchiaro, I Colombo, B Garavaglia, et al.Pageof 5