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Ikuya Nonaka

Showing results (41-50 of 169) with videos related to

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Brain & Development|October 30, 2012
Intranuclear rods myopathy with autonomic dysfunctionPo-Ching Chou, Wen-Chen Liang, Ikuya Nonaka, et al.
Brain & Development|December 17, 2009
A case of intraneural perineurioma presenting with monomelic atrophy in a childAyako Miyahara-Katayama, Yasushi Ohya, Tsuyoshi Omi, et al.
Mitochondrion|August 27, 2005
A novel mtDNA C11777A mutation in Leigh syndromeHirofumi Komaki, Jun Akanuma, Hideki Iwata, et al.
Neuromuscular Disorders : NMD|October 28, 2008
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1)Sherine Shalaby, Yukiko K Hayashi, Kanako Goto, et al.
Neuromuscular Disorders : NMD|March 28, 2006
Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1Adrian Phillip Scott, Richard James Nigel Allcock, Frank Mastaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 13, 2013
Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)Anna Cho, Yukiko K Hayashi, Kazunari Monma, et al.
Neurology|December 16, 2014
DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycanMingrui Dong, Satoru Noguchi, Yukari Endo, et al.
Brain & Development|January 18, 2006
A case of congenital neuromuscular disease with uniform type 1 fibersHaruko Maeda Sakamoto, Mieko Yoshioka, Masahiro Tsuji, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 5, 2003
Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathyKiyotaka Suwa, Masashi Mizuguchi, Mariko Y Momoi, et al.
Journal of Human Genetics|February 1, 2003
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathyMasakazu Mimaki, Akemi Ikota, Aya Sato, et al.
Pageof 17

Showing results (41-50 of 169) with videos related to

Sort By:
Pageof 17
Brain & Development|October 30, 2012
Intranuclear rods myopathy with autonomic dysfunctionPo-Ching Chou, Wen-Chen Liang, Ikuya Nonaka, et al.
Brain & Development|December 17, 2009
A case of intraneural perineurioma presenting with monomelic atrophy in a childAyako Miyahara-Katayama, Yasushi Ohya, Tsuyoshi Omi, et al.
Mitochondrion|August 27, 2005
A novel mtDNA C11777A mutation in Leigh syndromeHirofumi Komaki, Jun Akanuma, Hideki Iwata, et al.
Neuromuscular Disorders : NMD|October 28, 2008
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1)Sherine Shalaby, Yukiko K Hayashi, Kanako Goto, et al.
Neuromuscular Disorders : NMD|March 28, 2006
Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1Adrian Phillip Scott, Richard James Nigel Allcock, Frank Mastaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 13, 2013
Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy)Anna Cho, Yukiko K Hayashi, Kazunari Monma, et al.
Neurology|December 16, 2014
DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycanMingrui Dong, Satoru Noguchi, Yukari Endo, et al.
Brain & Development|January 18, 2006
A case of congenital neuromuscular disease with uniform type 1 fibersHaruko Maeda Sakamoto, Mieko Yoshioka, Masahiro Tsuji, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 5, 2003
Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathyKiyotaka Suwa, Masashi Mizuguchi, Mariko Y Momoi, et al.
Journal of Human Genetics|February 1, 2003
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathyMasakazu Mimaki, Akemi Ikota, Aya Sato, et al.
Pageof 17