Clinical phenotype and the G11778A mutation of mitochondrial DNA in patients with Leber's hereditary optic neuropathy in Taiwan

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Neuro-Ophthalmology, Vol. 26, Iss. 4, 2001-12 ,pp. : 207-216

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`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

By Lodi R.  

Brain, Vol. 123, Iss. 9, 2000-09 ,pp. : 1896-1902

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Bilateral sequential non-arteritic anterior ischemic optic neuropathy in incomplete Reiter's syndrome

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Neuro-Ophthalmology, Vol. 28, Iss. 4, 2004-10 ,pp. : 191-194

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Multiple Myeloma Presenting as Bilateral Posterior Optic Neuropathy

By Muñoz Silvia   Acebes Xènia   Arruga Jorge   Vidaller Antonio   Majós Carles   Sarrà Josep  

Neuro-Ophthalmology, Vol. 34, Iss. 5-6, 2010-12 ,pp. : 351-355

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Multicenter study on the frequency of three primary mutations of mitochondrial DNA in Japanese pedigrees with Leber's hereditary optic neuropathy: comparison with American and British counterparts

By Yamada Keiko   Oguchi Yoshihisa   Hotta Yoshihiro   Nakamura Makoto   Isashiki Yasushi   Mashima Yukihiko  

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