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收藏Novel Aspects of Hereditary Spastic Paraplegia: A Clinicopathologic and Biochemical Study of a Patient With a Heterozygous GCH1 Variant
Hongo, Shoko; Ikeda, Tetsuhiko; Tada, Mari; Aida, Rina; Ozawa, Tetsuo; Hara, Norikazu; Miyashita, Akinori; Nakajima, Takashi; Onodera, Osamu; Ikeuchi, Takeshi; Ichinose, Hiroshi; Kakita, Akiyoshi
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收藏Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation
Hayashi, Hideki; Saito, Rie; Tanaka, Hidetomo; Hara, Norikazu; Koide, Shin; Yonemochi, Yosuke; Ozawa, Tetsuo; Hokari, Mariko; Toyoshima, Yasuko; Miyashita, Akinori; Onodera, Osamu; Okamoto, Kouichirou; Ikeuchi, Takeshi; Nakajima, Takashi; Kakita, Akiyoshi
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收藏Percutaneous endoscopic gastrostomy procedure in patients with advanced duchenne muscular dystrophy
Aida, I.; Miyoshi, M.; Endo, H.; Tobinaga, M.; Ikeda, T.; Oota, K.; Yonemochi, Y.; Takahara, M.; Kanaya, H.; Ozawa, T.; Nakajima, T.
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收藏A case of sporadic amyotrophic lateral sclerosis presenting with chorea as the initial symptom
Ohta, K.; Ito, J.; Shimizu, H.; Takahashi, H.; Kakita, A.; Tobinaga, M.; Endo, H.; Ikeda, T.; Aida, I.; Yonemoti, Y.; Ozawa, T.; Nakajima, T.
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收藏Prognostic impact of venous thromboembolism in patients with Duchenne muscular dystrophy: Prospective multicenter 5-year cohort study
Kimura, Koichi; Morita, Hiroyuki; Daimon, Masao; Kawata, Takayuki; Nakao, Tomoko; Lee, Seitetsu L.; Hirokawa, Megumi; Ebihara, Aya; Nakajima, Takashi; Ozawa, Tetsuo; Yonemochi, Yosuke; Aida, Izumi; Motoyoshi, Yasufumi; Mikata, Takashi; Uchida, Idai; Komori, Tetsuo; Kitao, Ruriko; Nagata, Tetsuya; Takeda, Shin'ichi; Komaki, Hirofumi; Segawa, Kazuhiko; Takenaka, Katsu; Komuro, Issei
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收藏Prognostic impact of left ventricular noncompaction in patients with Duchenne/Becker muscular dystrophy - Prospective multicenter cohort study左心室心肌致密化不全对Duchenne/Becker型肌营养不良患者预后的影响 -- 前瞻性多中心队列研究
Kimura, Koichi; Takenaka, Katsu; Ebihara, Aya; Uno, Kansei; Morita, Hiroyuki; Nakajima, Takashi; Ozawa, Tetsuo; Aida, Izumi; Yonemochi, Yosuke; Higuchi, Shinya; Motoyoshi, Yasufumi; Mikata, Takashi; Uchida, Idai; Ishihara, Tadayuki; Komori, Tetsuo; Kitao, Ruriko; Nagata, Tetsuya; Takeda, Shin'ichi; Yatomi, Yutaka; Nagai, Ryozo; Komuro, Issei
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收藏Identification of a novel amino acid deletion mutation and a very rare single nucleotide variant in a Japanese family with type I antithrombin deficiency
Katayama, K; Hashimoto, N; Tanaka, Y; Ozawa, T; Emi, Y; Ikeda, T; Katayama, M; Nomura, S; Kitajima, I; Nakano, T; Imanaka, T
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收藏Intracellular accumulation of antithrombin Morioka (C95R), a novel mutation causing type I antithrombin deficiency
Tanaka, Y; Ueda, K; Ozawa, T; Sakuragawa, N; Yokota, S; Sato, R; Okamura, S; Morita, M; Imanaka, T
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