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Neurologic Clinics|August 1, 1990
Mitochondrial encephalomyopathiesS DiMauro, E Bonilla, A Lombes, et al.Brain Pathology (Zurich, Switzerland)|April 1, 1992
New morphological approaches to the study of mitochondrial encephalomyopathiesE Bonilla, M Sciacco, K Tanji, et al.Science (New York, N.Y.)|April 21, 1989
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNAE A Schon, R Rizzuto, C T Moraes, et al.American Journal of Human Genetics|March 1, 1990
Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisH Nakase, C T Moraes, R Rizzuto, et al.Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.Nature Genetics|July 1, 1993
A mitochondrial tRNA anticodon swap associated with a muscle diseaseC T Moraes, F Ciacci, E Bonilla, et al.Lancet (London, England)|March 2, 1991
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathyE Arnaudo, M Dalakas, S Shanske, et al.The American Journal of Pathology|September 1, 1988
Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patientsA F Miranda, E Bonilla, G Martucci, et al.Pediatric Research|October 6, 1997
A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathyA Verma, D A Piccoli, E Bonilla, et al.Annals of Neurology|June 1, 1991
Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromesM L Zupanc, C T Moraes, S Shanske, et al.Pageof 9