Hirano M - Search Results

1

Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions.

Carrozzo R, Davidson MM, Walker WF, Hirano M, Miranda AF. Carrozzo R, et al. Among authors: hirano m. J Neurol Sci. 1999 Nov 15;170(1):24-31. doi: 10.1016/s0022-510x(99)00193-8. J Neurol Sci. 1999. PMID: 10540032 Free article.

2

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

3

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.

4

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.

5

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.

6

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

7

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

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

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

10

Mitochondrial dysfunction as a mechanism of CNS injury.

DiMauro S, Simonetti S, Chen X, Petruzzella V, Hirano M, Shanske S, Moraes CT, Schon EA. DiMauro S, et al. Among authors: hirano m. Res Publ Assoc Res Nerv Ment Dis. 1993;71:67-79. Res Publ Assoc Res Nerv Ment Dis. 1993. PMID: 8417473 Review. No abstract available.

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