Hirano M - Search Results

1

Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegia.

Rowland LP, Hirano M, DiMauro S, Schon EA. Rowland LP, et al. Among authors: hirano m. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S15-21. doi: 10.1016/s0960-8966(97)00076-x. Neuromuscul Disord. 1997. PMID: 9392010 Review.

2

Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase.

Arnaudo E, Hirano M, Seelan RS, Milatovich A, Hsieh CL, Fabrizi GM, Grossman LI, Francke U, Schon EA. Arnaudo E, et al. Among authors: hirano m. Gene. 1992 Oct 1;119(2):299-305. doi: 10.1016/0378-1119(92)90287-y. Gene. 1992. PMID: 1327965 Free article.

3

Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidase.

Fabrizi GM, Sadlock J, Hirano M, Mita S, Koga Y, Rizzuto R, Zeviani M, Schon EA. Fabrizi GM, et al. Among authors: hirano m. Gene. 1992 Oct 1;119(2):307-12. doi: 10.1016/0378-1119(92)90288-z. Gene. 1992. PMID: 1327966

4

Melas: an original case and clinical criteria for diagnosis.

Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP. Hirano M, et al. Neuromuscul Disord. 1992;2(2):125-35. doi: 10.1016/0960-8966(92)90045-8. Neuromuscul Disord. 1992. PMID: 1422200 Review.

5

Epilepsy in mitochondrial encephalomyopathies.

DiMauro S, Ricci E, Hirano M, DeVivo DC. DiMauro S, et al. Among authors: hirano m. Epilepsy Res Suppl. 1991;4:173-80. Epilepsy Res Suppl. 1991. PMID: 1815599 Review. No abstract available.

6

Clinical syndromes associated with ragged red fibers.

Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Rowland LP, et al. Among authors: hirano m. Rev Neurol (Paris). 1991;147(6-7):467-73. Rev Neurol (Paris). 1991. PMID: 1962052

7

Mitochondrial encephalomyopathies: clinical and molecular analysis.

Schon EA, Hirano M, DiMauro S. Schon EA, et al. Among authors: hirano m. J Bioenerg Biomembr. 1994 Jun;26(3):291-9. doi: 10.1007/BF00763100. J Bioenerg Biomembr. 1994. PMID: 8077182 Review.

8

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Lovelace RE, Rowland LP, Schon EA, DiMauro S. Moraes CT, et al. Among authors: hirano m. J Clin Invest. 1993 Dec;92(6):2906-15. doi: 10.1172/JCI116913. J Clin Invest. 1993. PMID: 8254046 Free PMC article.

9

Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical study.

Sparaco M, Hirano A, Hirano M, DiMauro S, Bonilla E. Sparaco M, et al. Among authors: hirano m, hirano a. Brain Pathol. 1993 Oct;3(4):349-54. doi: 10.1111/j.1750-3639.1993.tb00762.x. Brain Pathol. 1993. PMID: 8293191

10

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA.

Moraes CT, Ciacci F, Silvestri G, Shanske S, Sciacco M, Hirano M, Schon EA, Bonilla E, DiMauro S. Moraes CT, et al. Among authors: hirano m. Neuromuscul Disord. 1993 Jan;3(1):43-50. doi: 10.1016/0960-8966(93)90040-q. Neuromuscul Disord. 1993. PMID: 8392410

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