Hirano M - Search Results

1

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.

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

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: clinical features, biochemistry, and molecular genetics.

Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, et al. Ciafaloni E, et al. Among authors: hirano m. Ann Neurol. 1992 Apr;31(4):391-8. doi: 10.1002/ana.410310408. Ann Neurol. 1992. PMID: 1586140

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

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts.

Hirano M, Pavlakis SG. Hirano M, et al. J Child Neurol. 1994 Jan;9(1):4-13. doi: 10.1177/088307389400900102. J Child Neurol. 1994. PMID: 8151079 Review.

9

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.

Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE, et al. Hirano M, et al. Neurology. 1994 Apr;44(4):721-7. doi: 10.1212/wnl.44.4.721. Neurology. 1994. PMID: 8164833

10

Mitochondrial DNA mutations in an outbreak of optic neuropathy in Cuba.

Hirano M, Cleary JM, Stewart AM, Lincoff NS, Odel JG, Santiesteban R, Santiago Luis R. Hirano M, et al. Neurology. 1994 May;44(5):843-5. doi: 10.1212/wnl.44.5.843. Neurology. 1994. PMID: 8190285

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