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Mitochondrial myopathies.
DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. DiMauro S, et al. Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602. Ann Neurol. 1985. PMID: 3927817 Review.
Genetic heterogeneity in Leigh syndrome.
DiMauro S, De Vivo DC. DiMauro S, et al. Among authors: de vivo dc. Ann Neurol. 1996 Jul;40(1):5-7. doi: 10.1002/ana.410400104. Ann Neurol. 1996. PMID: 8687192 No abstract available.
Clinical manifestations of mitochondrial DNA depletion.
Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728
Mitochondrial defects of brain and muscle.
De Vivo DC, DiMauro S. De Vivo DC, et al. Biol Neonate. 1990;58 Suppl 1:54-69. doi: 10.1159/000243300. Biol Neonate. 1990. PMID: 2265220 Review.
345 results