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Journal of the Neurological Sciences|December 19, 2008
Progressive carotid artery stenosis with a novel tRNA phenylalanine mitochondrial DNA mutationTakahiro Iizuka, Yu-ichi Goto, Saori Miyakawa, 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.
Parkinsonism & Related Disorders|May 16, 2013
Neuromelanin MRI in a family with mitochondrial parkinsonism harboring a Y955C mutation in POLG1Masako Mukai, Keizo Sugaya, Ichiro Yabe, et al.
Cell Communication and Signaling : CCS|June 2, 2023
LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditionsYoshinori Aoki, Hongmei Dai, Fumika Furuta, et al.
Brain & Development|April 27, 2016
Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in JapanMasahide Goto, Hirofumi Komaki, Eri Takeshita, et al.
Differentiation; Research in Biological Diversity|June 12, 2010
Partial loss of pancreas endocrine and exocrine cells of human ARX-null mutation: consideration of pancreas differentiationMasayuki Itoh, Yuji Takizawa, Sae Hanai, et al.
Brain & Development|April 16, 2013
MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNA(Leu(UUR)) geneMasahide Goto, Hirofumi Komaki, Takashi Saito, 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.
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.
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