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Page 1
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.
Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Among authors: dimauro s. Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339. Neurology. 1988. PMID: 3412580
Genetic heterogeneity in Leigh syndrome.
DiMauro S, De Vivo DC. DiMauro S, et al. 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. Among authors: dimauro s. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728
Cerebral lactic acidosis correlates with neurological impairment in MELAS.
Kaufmann P, Shungu DC, Sano MC, Jhung S, Engelstad K, Mitsis E, Mao X, Shanske S, Hirano M, DiMauro S, De Vivo DC. Kaufmann P, et al. Among authors: dimauro s. Neurology. 2004 Apr 27;62(8):1297-302. doi: 10.1212/01.wnl.0000120557.83907.a8. Neurology. 2004. PMID: 15111665 Clinical Trial.
735 results