Hirano M - Search Results

1

Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

Bohlega S, Tanji K, Santorelli FM, Hirano M, al-Jishi A, DiMauro S. Bohlega S, et al. Among authors: hirano m. Neurology. 1996 May;46(5):1329-34. doi: 10.1212/wnl.46.5.1329. Neurology. 1996. PMID: 8628476

2

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.

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

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

5

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.

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

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.

8

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

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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