نتائج البحث - Yoshimura, Akiko

Effectiveness of drug safety measures for reducing the incidence of adverse drug reactions: Post-hoc analysis of data from all-case surveillance of iguratimod using generalized est... حسب Shibata, Kai, Yoshimura, Akiko, Ikeuchi, Satoshi, Ishii, Mika

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Clinical presentation of axial myopathy in two siblings with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP) حسب Matsuura, Eiji, Yoshimura, Akiko, Nozuma, Satoshi, Higuchi, Itsuro, Kubota, Ryuji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene حسب Lee, Jinhee, Iwasaki, Takuya, Kaida, Tomoko, Chuman, Hideki, Yoshimura, Akiko, Okamoto, Yuji, Takashima, Hiroshi, Miyata, Kazunori

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan حسب Yoshimura, Akiko, Yuan, Jun-Hui, Hashiguchi, Akihiro, Ando, Masahiro, Higuchi, Yujiro, Nakamura, Tomonori, Okamoto, Yuji, Nakagawa, Masanori, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Recurrence of Left Ventricular Outflow Tract Obstruction Requiring Alcohol Septal Ablation after Transcatheter Aortic Valve Implantation حسب Kitahara, Hideki, Matsuura, Kaoru, Sugiura, Atsushi, Yoshimura, Akiko, Muramatsu, Takahiro, Tamura, Yusaku, Nakayama, Takashi, Fujimoto, Yoshihide, Matsumiya, Goro, Kobayashi, Yoshio

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

An MFN2-related Charcot-Marie-Tooth Disease Patient with Optic Nerve Atrophy, Neurogenic Bladder Dysfunction, and Diaphragmatic Weakness حسب Kimura, Yasuyoshi, Nishikawa, Akira, Hashiguchi, Akihiro, Etoh, Masaki, Yoshimura, Akiko, Asai, Kanako, Miyashita, Noriko, Takashima, Hiroshi, Sumi, Hisae, Naka, Takashi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Peripheral neuropathy in a case with CADASIL: a case report حسب Sakiyama, Yusuke, Matsuura, Eiji, Maki, Yoshimitsu, Yoshimura, Akiko, Ando, Masahiro, Nomura, Miwa, Shinohara, Kazuya, Saigo, Ryuji, Nakamura, Tomonori, Hashiguchi, Akihiro, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins حسب Sawada, Jun, Katayama, Takayuki, Tokashiki, Takashi, Kikuchi, Shiori, Kano, Kohei, Takahashi, Kae, Saito, Tsukasa, Adachi, Yoshiki, Okamoto, Yuji, Yoshimura, Akiko, Takashima, Hiroshi, Hasebe, Naoyuki

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Benzalkonium Chloride Resistance in Staphylococcus epidermidis on the Ocular Surface of Glaucoma Patients Under Long-Term Administration of Eye Drops حسب Lee, Jinhee, Iwasaki, Takuya, Ohtani, Shinichiro, Matsui, Hidehito, Nejima, Ryohei, Mori, Yosai, Kagaya, Fumie, Yagi, Akiko, Yoshimura, Akiko, Hanaki, Hideaki, Aihara, Makoto, Miyata, Kazunori

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study حسب Ando, Masahiro, Hashiguchi, Akihiro, Okamoto, Yuji, Yoshimura, Akiko, Hiramatsu, Yu, Yuan, Junhui, Higuchi, Yujiro, Mitsui, Jun, Ishiura, Hiroyuki, Umemura, Ayako, Maruyama, Koichi, Matsushige, Takeshi, Morishita, Shinichi, Nakagawa, Masanori, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan حسب Taniguchi, Takaki, Ando, Masahiro, Okamoto, Yuji, Yoshimura, Akiko, Higuchi, Yujiro, Hashiguchi, Akihiro, Shiga, Kensuke, Hayashida, Arisa, Hatano, Taku, Ishiura, Hiroyuki, Mitsui, Jun, Hattori, Nobutaka, Mizuno, Toshiki, Nakagawa, Masanori, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

The application of shotgun metagenomics to the diagnosis of granulomatous amoebic encephalitis due to Balamuthia mandrillaris: a case report حسب Hirakata, Shota, Sakiyama, Yusuke, Yoshimura, Akiko, Ikeda, Mei, Takahata, Katsunori, Tashiro, Yuichi, Yoshimura, Michiyoshi, Arata, Hitoshi, Yonezawa, Hajime, Kirishima, Mari, Higashi, Michiyo, Hatanaka, Miho, Kanekura, Takuro, Yagita, Kenji, Matsuura, Eiji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan حسب Ando, Masahiro, Higuchi, Yujiro, Yuan, Jun‐Hui, Yoshimura, Akiko, Kitao, Ruriko, Morimoto, Takehiko, Taniguchi, Takaki, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible حسب Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Kojima, Fumikazu, Noguchi, Yutaka, Hobara, Takahiro, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease حسب Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Takei, Jun, Takeuchi, Mika, Hiramatsu, Yu, Shimizu, Fumitaka, Kubota, Masaya, Takeshima, Akari, Ueda, Takehiro, Koh, Kishin, Nagaoka, Utako, Tokashiki, Takashi, Sawai, Setsu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Sato, Ryota, Kanda, Takashi, Okamoto, Yuji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan حسب Tanabe, Hajime, Higuchi, Yujiro, Yuan, Jun‐Hui, Hashiguchi, Akihiro, Yoshimura, Akiko, Ishihara, Satoshi, Nozuma, Satoshi, Okamoto, Yuji, Matsuura, Eiji, Ishiura, Hiroyuki, Mitsui, Jun, Takashima, Ryotaro, Kokubun, Norito, Maeda, Kengo, Asano, Yuri, Sunami, Yoko, Kono, Yu, Ishigaki, Yasunori, Yanamoto, Shosaburo, Fukae, Jiro, Kida, Hiroshi, Morita, Mitsuya, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes حسب Hiramatsu, Yu, Okamoto, Yuji, Yoshimura, Akiko, Yuan, Jun-Hui, Ando, Masahiro, Higuchi, Yujiro, Hashiguchi, Akihiro, Matsuura, Eiji, Nozaki, Fumihito, Kumada, Tomohiro, Murayama, Kei, Suzuki, Mikiya, Yamamoto, Yuki, Matsui, Naoko, Miyazaki, Yoshimichi, Yamaguchi, Masamitsu, Suzuki, Youji, Mitsui, Jun, Ishiura, Hiroyuki, Tanaka, Masaki, Morishita, Shinichi, Nishino, Ichizo, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy حسب Higuchi, Yujiro, Okunushi, Ryuta, Hara, Taichi, Hashiguchi, Akihiro, Yuan, Junhui, Yoshimura, Akiko, Murayama, Kei, Ohtake, Akira, Ando, Masahiro, Hiramatsu, Yu, Ishihara, Satoshi, Tanabe, Hajime, Okamoto, Yuji, Matsuura, Eiji, Ueda, Takehiro, Toda, Tatsushi, Yamashita, Sumimasa, Yamada, Kenichiro, Koide, Takashi, Yaguchi, Hiroaki, Mitsui, Jun, Ishiura, Hiroyuki, Yoshimura, Jun, Doi, Koichiro, Morishita, Shinichi, Sato, Ken, Nakagawa, Masanori, Yamaguchi, Masamitsu, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan حسب Sakiyama, Yusuke, Kanda, Naoaki, Higuchi, Yujiro, Yoshimura, Michiyoshi, Wakaguri, Hiroyuki, Takata, Yoshiharu, Watanabe, Osamu, Yuan, Junhui, Tashiro, Yuichi, Saigo, Ryuji, Nozuma, Satoshi, Yoshimura, Akiko, Arishima, Shiho, Ikeda, Kenichi, Shinohara, Kazuya, Arata, Hitoshi, Michizono, Kumiko, Higashi, Keiko, Hashiguchi, Akihiro, Okamoto, Yuji, Hirano, Ryuki, Shiraishi, Tadafumi, Matsuura, Eiji, Okubo, Ryuichi, Higuchi, Itsuro, Goto, Masamichi, Hirano, Hirofumi, Sano, Akira, Iwasaki, Takuya, Matsuda, Fumihiko, Izumo, Shuji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل

Mutations in MME cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2 حسب Higuchi, Yujiro, Hashiguchi, Akihiro, Yuan, Junhui, Yoshimura, Akiko, Mitsui, Jun, Ishiura, Hiroyuki, Tanaka, Masaki, Ishihara, Satoshi, Tanabe, Hajime, Nozuma, Satoshi, Okamoto, Yuji, Matsuura, Eiji, Ohkubo, Ryuichi, Inamizu, Saeko, Shiraishi, Wataru, Yamasaki, Ryo, Ohyagi, Yasumasa, Kira, Jun‐ichi, Oya, Yasushi, Yabe, Hayato, Nishikawa, Noriko, Tobisawa, Shinsuke, Matsuda, Nozomu, Masuda, Masayuki, Kugimoto, Chiharu, Fukushima, Kazuhiro, Yano, Satoshi, Yoshimura, Jun, Doi, Koichiro, Nakagawa, Masanori, Morishita, Shinichi, Tsuji, Shoji, Takashima, Hiroshi

احصل على النص الكامل احصل على النص الكامل احصل على النص الكامل