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Brain & Development|May 1, 1996
Clinical and EEG findings in eleven patients affected by mitochondrial encephalomyopathy with MERRF-MELAS overlapG Serra, R Piccinnu, M Tondi, et al.Genomics|January 8, 1999
Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chainV Petruzzella, V Tiranti, P Fernandez, et al.Journal of Neurology|October 1, 1994
The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patientsM Eoli, M Pandolfo, C Milanese, et al.Biochimica Et Biophysica Acta|May 24, 1995
Searching for genes affecting the structural integrity of the mitochondrial genomeM Zeviani, P Amati, G Comi, 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.Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, 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.Mitochondrion|February 8, 2012
Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cellsF Invernizzi, I D'Amato, P B Jensen, et al.Muscle & Nerve. Supplement|January 1, 1995
OXPHOS defects and mitochondrial DNA mutations in cardiomyopathyM Zeviani, C Mariotti, C Antozzi, et al.Human Molecular Genetics|November 11, 1999
Characterization of SURF-1 expression and Surf-1p function in normal and disease conditionsV Tiranti, C Galimberti, L Nijtmans, et al.Pageof 18