Hirano M - Search Results

1

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.

Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Sproule DM, Battista V, Koenigsberger DY, Pascual JM, Shanske S, Sano M, Mao X, Hirano M, Shungu DC, Dimauro S, De Vivo DC. Kaufmann P, et al. Among authors: hirano m. Neurology. 2011 Nov 29;77(22):1965-71. doi: 10.1212/WNL.0b013e31823a0c7f. Epub 2011 Nov 16. Neurology. 2011. PMID: 22094475 Free PMC article.

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

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

4

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.

5

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

6

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.

7

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.

8

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

9

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

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,303 results

Search Page

Filters