Search Results - Ozawa, Matsuko

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  1. 1
    Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family

    Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family by Tojo, Megumu, Ozawa, Matsuko, Nonaka, Ikuya

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  2. 2
    Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers (MERRF): a single-photon emission computed tomographic (SPECT) and electrophysiological study

    Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers (MERRF): a single-photon emission computed tomographic (SPECT) and electrop... by Tanaka, Soichiro, Osaria, Shin-ichi, Ozawa, Matsuko, Yamanouchi, Hideo, Goto, Yu-ichi, Matsuda, Hiroshi, Nonaka, Ikuya

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  3. 3
    Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families

    Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families by Ozawa, M, Nishino, I, Horai, S, Nonaka, I, Goto, Y I

    Published in Muscle & nerve
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  4. 4
    Single muscle fiber analysis in patients with 3243 mutation in mitochondrial DNA: Comparison with the phenotype and the proportion of mutant genome

    Single muscle fiber analysis in patients with 3243 mutation in mitochondrial DNA: Comparison with the phenotype and the proportion of mutant genome by Ozawa, Matsuko, Nonaka, Ikuya, Goto, Yu-ichi

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  5. 5
    Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA super(Lys) in two families

    Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA super(Lys) in two families by Ozawa, Matsuko, Nishino, Ichizo, Horai, Satoshi, Nonaka, Ikuya, Goto, Yu-Ichi

    Published in Muscle & nerve
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  6. 6
    The 8,344 mutation in mitochondrial DNA: A comparison between the proportion of mutant DNA and clinico-pathologic findings

    The 8,344 mutation in mitochondrial DNA: A comparison between the proportion of mutant DNA and clinico-pathologic findings by Ozawa, Matsuko, Goto, Yu-Ichi, Sakuta, Ryoichi, Tanno, Yoshinori, Tsuji, Shoji, Nonaka, Ikuya

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  7. 7
    Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNALys in two families

    Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNALys in two families by Ozawa, Matsuko, Nishino, Ichizo, Horai, Satoshi, Nonaka, Ikuya, Goto, Yu-Ichi

    Published in Muscle & nerve
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  8. 8
    Severe Central Nervous System Involvement in a Patient With Congenital Fiber-Type Disproportion Myopathy

    Severe Central Nervous System Involvement in a Patient With Congenital Fiber-Type Disproportion Myopathy by Nakagawa, Eiji, Ozawa, Matsuko, Yamanouchi, Hideo, Sugai, Kenji, Goto, Yu-ichi, Nonaka, Ikuya

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