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Cardiovascular Research|August 30, 2000
Aging is associated with increased lipid peroxidation in human hearts, but not with mitochondrial respiratory chain enzyme defectsO Miró, J Casademont, E Casals, et al.
FEBS Letters|August 28, 1998
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesisP Cantatore, V Petruzzella, C Nicoletti, et al.
Clinical and Experimental Pharmacology & Physiology|April 1, 1995
Use of primary cultures and continuous cell lines to study effects on astrocytic regulatory functionsE Walum, G Eriksson, A Peterson, et al.
American Journal of Human Genetics|December 1, 1992
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeN G Larsson, M H Tulinius, E Holme, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 17, 2004
Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiencyM A Kurian, E S O'Mahoney, P Rustin, et al.
Pediatrics|November 3, 2005
Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patientsA García-Cazorla, P De Lonlay, M C Nassogne, et al.
Human Genetics|September 1, 1995
De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspringM H Tulinius, M Houshmand, N G Larsson, et al.
The Biochemical Journal|February 28, 1998
Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changesD Chretien, J Gallego, A Barrientos, et al.
The British Journal of Dermatology|June 22, 2010
Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth diseaseM Marque, B Gardie, B Bressac de Paillerets, et al.
Lancet (London, England)|August 28, 1999
Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary studyP Rustin, J C von Kleist-Retzow, K Chantrel-Groussard, et al.
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