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Neurology|July 1, 1996
Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscleH A Bentlage, U Wendel, H Schägger, et al.
European Journal of Biochemistry|January 15, 1995
Kinetic properties and ligand binding of the eleven-subunit cytochrome-c oxidase from Saccharomyces cerevisiae isolated with a novel large-scale purification methodB M Geier, H Schägger, C Ortwein, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 4, 1999
Altered gene expression and functions of mitochondria in human nephrotic syndromeH Holthöfer, M Kretzler, A Haltia, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Biochimica Et Biophysica Acta|March 8, 1995
Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathiesH A Bentlage, A J Janssen, A Chomyn, et al.
Neuromuscular Disorders : NMD|December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantationF M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Biochemistry|April 12, 1994
Characterization of the chloroplast cytochrome b6f complex as a structural and functional dimerD Huang, R M Everly, R H Cheng, et al.
Annals of Neurology|January 23, 1999
A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndromeI F De Coo, W O Renier, W Ruitenbeek, et al.
Neurology|March 14, 2001
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeR Carrozzo, A Tessa, M E Vázquez-Memije, et al.
Neuromuscular Disorders : NMD|August 30, 2001
Respiratory chain defects in hereditary spastic paraplegiasF Piemonte, C Casali, R Carrozzo, et al.
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