Hirano M - Search Results

1

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

Salviati L, Sacconi S, Murer L, Zacchello G, Franceschini L, Laverda AM, Basso G, Quinzii C, Angelini C, Hirano M, Naini AB, Navas P, DiMauro S, Montini G. Salviati L, et al. Among authors: hirano m. Neurology. 2005 Aug 23;65(4):606-8. doi: 10.1212/01.wnl.0000172859.55579.a7. Neurology. 2005. PMID: 16116126

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

Glycogen branching enzyme deficiency in adult polyglucosan body disease.

Bruno C, Servidei S, Shanske S, Karpati G, Carpenter S, McKee D, Barohn RJ, Hirano M, Rifai Z, DiMauro S. Bruno C, et al. Among authors: hirano m. Ann Neurol. 1993 Jan;33(1):88-93. doi: 10.1002/ana.410330114. Ann Neurol. 1993. PMID: 8494336

6

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

7

Mitochondrial DNA and RNA processing in MELAS.

Kaufmann P, Koga Y, Shanske S, Hirano M, DiMauro S, King MP, Schon EA. Kaufmann P, et al. Among authors: hirano m. Ann Neurol. 1996 Aug;40(2):172-80. doi: 10.1002/ana.410400208. Ann Neurol. 1996. PMID: 8773598

8

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency.

Sobreira C, Hirano M, Shanske S, Keller RK, Haller RG, Davidson E, Santorelli FM, Miranda AF, Bonilla E, Mojon DS, Barreira AA, King MP, DiMauro S. Sobreira C, et al. Among authors: hirano m. Neurology. 1997 May;48(5):1238-43. doi: 10.1212/wnl.48.5.1238. Neurology. 1997. PMID: 9153450

9

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

Manfredi G, Vu T, Bonilla E, Schon EA, DiMauro S, Arnaudo E, Zhang L, Rowland LP, Hirano M. Manfredi G, et al. Among authors: hirano m. Ann Neurol. 1997 Aug;42(2):180-8. doi: 10.1002/ana.410420208. Ann Neurol. 1997. PMID: 9266727

10

Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.

Carrozzo R, Hirano M, Fromenty B, Casali C, Santorelli FM, Bonilla E, DiMauro S, Schon EA, Miranda AF. Carrozzo R, et al. Among authors: hirano m. Neurology. 1998 Jan;50(1):99-106. doi: 10.1212/wnl.50.1.99. Neurology. 1998. PMID: 9443465

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