|
Mojon, D S; Herbert, J; Sadiq, S A et al. (1999) Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis. Ophthalmologica 213:171-5
|
|
Mojon, D S; Fujihara, K; Hirano, M et al. (1999) Leber's hereditary optic neuropathy mitochondrial DNA mutations in familial multiple sclerosis. Graefes Arch Clin Exp Ophthalmol 237:348-50
|
|
Hirano, M; Garcia-de-Yebenes, J; Jones, A C et al. (1998) Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter. Am J Hum Genet 63:526-33
|
|
Sobreira, C; Hirano, M; Shanske, S et al. (1997) Mitochondrial encephalomyopathy with coenzyme Q10 deficiency. Neurology 48:1238-43
|
|
Hirano, M; Shtilbans, A; Mayeux, R et al. (1997) Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes. Proc Natl Acad Sci U S A 94:14894-9
|
|
Bohlega, S; Tanji, K; Santorelli, F M et al. (1996) Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy. Neurology 46:1329-34
|
|
Hirano, M; Pavlakis, S G (1994) Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts. J Child Neurol 9:4-13
|
|
Hirano, M; Silvestri, G; Blake, D M et al. (1994) Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology 44:721-7
|
|
Hirano, M; Cleary, J M; Stewart, A M et al. (1994) Mitochondrial DNA mutations in an outbreak of optic neuropathy in Cuba. Neurology 44:843-5
|
|
Lincoff, N S; Odel, J G; Hirano, M (1993) 'Outbreak' of optic and peripheral neuropathy in Cuba? JAMA 270:511-8
|
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