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Page 1
TK2 mutation presenting as indolent myopathy.
Paradas C, Gutiérrez Ríos P, Rivas E, Carbonell P, Hirano M, DiMauro S. Paradas C, et al. Among authors: dimauro s. Neurology. 2013 Jan 29;80(5):504-6. doi: 10.1212/WNL.0b013e31827f0ff7. Epub 2013 Jan 9. Neurology. 2013. PMID: 23303857 Free PMC article.
Branching enzyme deficiency: expanding the clinical spectrum.
Paradas C, Akman HO, Ionete C, Lau H, Riskind PN, Jones DE, Smith TW, Hirano M, Dimauro S. Paradas C, et al. Among authors: dimauro s. JAMA Neurol. 2014 Jan;71(1):41-7. doi: 10.1001/jamaneurol.2013.4888. JAMA Neurol. 2014. PMID: 24248152 Free PMC article.
Pedaling from genotype to phenotype.
Dimauro S, Hirano M. Dimauro S, et al. Arch Neurol. 2006 Dec;63(12):1679-80. doi: 10.1001/archneur.63.12.1679. Arch Neurol. 2006. PMID: 17172605 No abstract available.
A diagnostic algorithm for metabolic myopathies.
Berardo A, DiMauro S, Hirano M. Berardo A, et al. Among authors: dimauro s. Curr Neurol Neurosci Rep. 2010 Mar;10(2):118-26. doi: 10.1007/s11910-010-0096-4. Curr Neurol Neurosci Rep. 2010. PMID: 20425236 Free PMC article. Review.
735 results