Search Results - Ruoyi Ishikawa
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Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented ga... by Ruoyi Ishikawa, Masahiro Nakamori, Megumi Takenaka, Shiro Aoki, Yu Yamazaki, Akihiro Hashiguchi, Hiroshi Takashima, Hirofumi Maruyama
Published in Frontiers in Neurology (2023-06-01)Get full text
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Swallowing sound evaluation using an electronic stethoscope and artificial intelligence analysis for patients with amyotrophic lateral sclerosis by Masahiro Nakamori, Ruoyi Ishikawa, Tomoaki Watanabe, Megumi Toko, Hiroyuki Naito, Tamayo Takahashi, Yoshitaka Simizu, Yu Yamazaki, Hirofumi Maruyama
Published in Frontiers in Neurology (2023-08-01)Get full text
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