Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

2,288 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Biochemical studies of patients with Cuban epidemic neuropathy.
Rodríguez-Hernandez M, Hirano M, Naini A, Santiestéban R. Rodríguez-Hernandez M, et al. Among authors: hirano m. Ophthalmic Res. 2001 Nov-Dec;33(6):310-3. doi: 10.1159/000055686. Ophthalmic Res. 2001. PMID: 11721182
[Molecular studies in Cuban patients with progressive external ophthalmoplegia].
Rodríguez-Hernández M, Hirano M, Arrieta T, Lestayo Z, Estrada R, Santiesteban R, Guerra-Badía R, Galarraga J, Gutierres J, Hechevarría E, Andreu A, Montoya J, DiMauro S. Rodríguez-Hernández M, et al. Among authors: hirano m. Rev Neurol. 2000 Jun 1-15;30(11):1001-5. Rev Neurol. 2000. PMID: 10904941 Spanish.
[Clinical manifestation and molecular identification of patients with Leber's hereditary optic neuropathy in a national reference center for neuro-ophthalmology in Cuba].
Santiesteban-Freixas R, Rodríguez-Hernández M, Mendoza-Santiesteban CE, Carrero-Salgado M, Francisco-Plasencia M, Méndez-Larramendi I, Vidal-Casalís S, Rivero-Reyes R, Hirano M. Santiesteban-Freixas R, et al. Among authors: hirano m. Rev Neurol. 1999 Sep 1-15;29(5):408-15. Rev Neurol. 1999. PMID: 10584242 Review. Spanish.
Human CoQ10 deficiencies.
Quinzii CM, López LC, Naini A, DiMauro S, Hirano M. Quinzii CM, et al. Among authors: hirano m. Biofactors. 2008;32(1-4):113-8. doi: 10.1002/biof.5520320113. Biofactors. 2008. PMID: 19096106 Free PMC article.
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
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
Mancuso M, Salviati L, Sacconi S, Otaegui D, Camaño P, Marina A, Bacman S, Moraes CT, Carlo JR, Garcia M, Garcia-Alvarez M, Monzon L, Naini AB, Hirano M, Bonilla E, Taratuto AL, DiMauro S, Vu TH. Mancuso M, et al. Among authors: hirano m. Neurology. 2002 Oct 22;59(8):1197-202. doi: 10.1212/01.wnl.0000028689.93049.9a. Neurology. 2002. PMID: 12391347
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
2,288 results