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2,090 results
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Primary coenzyme Q10 deficiency and the brain.
Naini A, Lewis VJ, Hirano M, DiMauro S. Naini A, et al. Among authors: hirano m. Biofactors. 2003;18(1-4):145-52. doi: 10.1002/biof.5520180217. Biofactors. 2003. PMID: 14695930
Mitochondrial encephalomyopathy with coenzyme Q10 deficiency.
Sobreira C, Hirano M, Shanske S, Keller RK, Haller RG, Davidson E, Santorelli FM, Miranda AF, Bonilla E, Mojon DS, Barreira AA, King MP, DiMauro S. Sobreira C, et al. Among authors: hirano m. Neurology. 1997 May;48(5):1238-43. doi: 10.1212/wnl.48.5.1238. Neurology. 1997. PMID: 9153450
Mitochondria in neuromuscular disorders.
DiMauro S, Bonilla E, Davidson M, Hirano M, Schon EA. DiMauro S, et al. Among authors: hirano m. Biochim Biophys Acta. 1998 Aug 10;1366(1-2):199-210. doi: 10.1016/s0005-2728(98)00113-3. Biochim Biophys Acta. 1998. PMID: 9714805 Review.
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.
Musumeci O, Naini A, Slonim AE, Skavin N, Hadjigeorgiou GL, Krawiecki N, Weissman BM, Tsao CY, Mendell JR, Shanske S, De Vivo DC, Hirano M, DiMauro S. Musumeci O, et al. Among authors: hirano m. Neurology. 2001 Apr 10;56(7):849-55. doi: 10.1212/wnl.56.7.849. Neurology. 2001. PMID: 11294920
Reversion of mtDNA depletion in a patient with TK2 deficiency.
Vilà MR, Segovia-Silvestre T, Gámez J, Marina A, Naini AB, Meseguer A, Lombès A, Bonilla E, DiMauro S, Hirano M, Andreu AL. Vilà MR, et al. Among authors: hirano m. Neurology. 2003 Apr 8;60(7):1203-5. doi: 10.1212/01.wnl.0000055928.58122.47. Neurology. 2003. PMID: 12682338
Cerebellar ataxia and coenzyme Q10 deficiency.
Lamperti C, Naini A, Hirano M, De Vivo DC, Bertini E, Servidei S, Valeriani M, Lynch D, Banwell B, Berg M, Dubrovsky T, Chiriboga C, Angelini C, Pegoraro E, DiMauro S. Lamperti C, et al. Among authors: hirano m. Neurology. 2003 Apr 8;60(7):1206-8. doi: 10.1212/01.wnl.0000055089.39373.fc. Neurology. 2003. PMID: 12682339
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