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Nature Genetics|November 4, 2000
Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetesJ P Silva, M Köhler, C Graff, et al.European Journal of Pediatrics|January 1, 1995
Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletionsM H Tulinius, A Oldfors, E Holme, et al.Nature Genetics|October 1, 1995
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyT Bourgeron, P Rustin, D Chretien, et al.Journal of Inherited Metabolic Disease|January 1, 1996
Clinical presentation of mitochondrial disorders in childhoodA Munnich, A Rötig, D Chretien, et al.Journal of the Neurological Sciences|April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiencyE Boitier, F Degoul, I Desguerre, et al.Pediatric Research|December 1, 1992
Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduriaE Holme, J Greter, C E Jacobson, et al.Journal of Inherited Metabolic Disease|April 5, 2001
Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenoneT Lerman-Sagie, P Rustin, D Lev, et al.The Journal of Pediatrics|May 1, 1997
Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationV Cormier-Daire, D Chretien, P Rustin, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1997
Severe complex I deficiency in a case of neonatal-onset lactic acidosis and fatal liver failureM Mazzella, R Cerone, W Bonacci, et al.The Journal of Pediatrics|April 1, 1995
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisA Rötig, F Goutières, P Niaudet, et al.Pageof 18