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Ikuya Nonaka

Showing results (91-100 of 169) with videos related to

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Journal of the Neurological Sciences|May 28, 2003
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patientsKazuhiko Tagawa, Megumu Ogawa, Kiyokazu Kawabe, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Congenital generalized lipodystrophy type 4 with muscular dystrophy: clinical and pathological manifestations in early childhoodNobuyuki Murakami, Yukiko K Hayashi, Yuji Oto, et al.
Orphanet Journal of Rare Diseases|April 24, 2014
A nationwide survey on Marinesco-Sjögren syndrome in JapanMasahide Goto, Mari Okada, Hirofumi Komaki, et al.
The American Journal of the Medical Sciences|May 17, 2005
Vascular involvement in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesNobuyuki Takahashi, Toshio Shimada, Yo Murakami, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 6, 2004
[MELAS-like episodes in an adult case with cytochrome c oxidase deficiency]Tameko Kihira, Junko Kohmoto, Sohei Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 2, 2006
[Molecular pathomechanism of distal myopathy with rimmed vacuoles]Ichizo Nishino, Satoru Noguchi, Kumiko Murayama, et al.
Plos One|December 20, 2012
Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathiesKazunari Momma, Satoru Noguchi, May Christine V Malicdan, et al.
Internal Medicine (Tokyo, Japan)|March 4, 2008
Mitochondrial encephalomyopathy associated with diabetes mellitus, cataract, and corpus callosum atrophyMinoru Oishi, Kenji Miki, Akihiko Morita, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathologyRie S Tsuburaya, Kazunari Monma, Yasushi Oya, et al.
Brain & Development|January 8, 2011
A case of congenital axonal neuropathy associated with West syndromeTomoko Mizuno, Masayuki Sasaki, Hirofumi Komaki, et al.
Pageof 17

Showing results (91-100 of 169) with videos related to

Sort By:
Pageof 17
Journal of the Neurological Sciences|May 28, 2003
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patientsKazuhiko Tagawa, Megumu Ogawa, Kiyokazu Kawabe, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Congenital generalized lipodystrophy type 4 with muscular dystrophy: clinical and pathological manifestations in early childhoodNobuyuki Murakami, Yukiko K Hayashi, Yuji Oto, et al.
Orphanet Journal of Rare Diseases|April 24, 2014
A nationwide survey on Marinesco-Sjögren syndrome in JapanMasahide Goto, Mari Okada, Hirofumi Komaki, et al.
The American Journal of the Medical Sciences|May 17, 2005
Vascular involvement in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodesNobuyuki Takahashi, Toshio Shimada, Yo Murakami, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 6, 2004
[MELAS-like episodes in an adult case with cytochrome c oxidase deficiency]Tameko Kihira, Junko Kohmoto, Sohei Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 2, 2006
[Molecular pathomechanism of distal myopathy with rimmed vacuoles]Ichizo Nishino, Satoru Noguchi, Kumiko Murayama, et al.
Plos One|December 20, 2012
Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathiesKazunari Momma, Satoru Noguchi, May Christine V Malicdan, et al.
Internal Medicine (Tokyo, Japan)|March 4, 2008
Mitochondrial encephalomyopathy associated with diabetes mellitus, cataract, and corpus callosum atrophyMinoru Oishi, Kenji Miki, Akihiko Morita, et al.
Neuromuscular Disorders : NMD|December 27, 2011
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathologyRie S Tsuburaya, Kazunari Monma, Yasushi Oya, et al.
Brain & Development|January 8, 2011
A case of congenital axonal neuropathy associated with West syndromeTomoko Mizuno, Masayuki Sasaki, Hirofumi Komaki, et al.
Pageof 17