Αποτελέσματα αναζήτησης - Okamoto, Yuji
- Εμφανίζονται 1 - 20 Αποτελέσματα από 27
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Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice από Okamoto, Yuji, Lipstein, Noa, Hua, Yunfeng, Lin, Kun-Han, Brose, Nils, Sakaba, Takeshi, Midorikawa, Mitsuharu
Έκδοση 2016Κείμενο -
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A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene από Lee, Jinhee, Iwasaki, Takuya, Kaida, Tomoko, Chuman, Hideki, Yoshimura, Akiko, Okamoto, Yuji, Takashima, Hiroshi, Miyata, Kazunori
Έκδοση 2022Κείμενο -
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Stenotic changes of the posterior cerebral artery are a major contributing factor for cerebral infarction in moyamoya disease από Ohkura, Akira, Negoto, Tetsuya, Aoki, Takachika, Noguchi, Kei, Okamoto, Yuji, Komatani, Hideki, Kawano, Takayuki, Mukasa, Akitake, Morioka, Motohiro
Έκδοση 2018Κείμενο -
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Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan από Yoshimura, Akiko, Yuan, Jun-Hui, Hashiguchi, Akihiro, Ando, Masahiro, Higuchi, Yujiro, Nakamura, Tomonori, Okamoto, Yuji, Nakagawa, Masanori, Takashima, Hiroshi
Έκδοση 2019Κείμενο -
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Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy από Kawashima, Kazuhiro, Okamoto, Yuji, Annayev, Orazmuhammet, Toyokura, Nobuo, Takahashi, Ryota, Lippmaa, Mikk, Itaka, Kenji, Suzuki, Yoshikazu, Matsuki, Nobuyuki, Koinuma, Hideomi
Έκδοση 2017Κείμενο -
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A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy από Sakiyama, Yusuke, Okamoto, Yuji, Higuchi, Itsuro, Inamori, Yukie, Sangatsuda, Yoko, Michizono, Kumiko, Watanabe, Osamu, Hatakeyama, Hideyuki, Goto, Yu-ichi, Arimura, Kimiyoshi, Takashima, Hiroshi
Έκδοση 2011Κείμενο -
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The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins από Sawada, Jun, Katayama, Takayuki, Tokashiki, Takashi, Kikuchi, Shiori, Kano, Kohei, Takahashi, Kae, Saito, Tsukasa, Adachi, Yoshiki, Okamoto, Yuji, Yoshimura, Akiko, Takashima, Hiroshi, Hasebe, Naoyuki
Έκδοση 2019Κείμενο -
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Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study από 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
Έκδοση 2017Κείμενο -
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Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan από 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
Έκδοση 2020Κείμενο -
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Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan από 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
Έκδοση 2022Κείμενο -
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Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible από 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
Έκδοση 2022Κείμενο -
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Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D από Okamoto, Yuji, Goksungur, Meryem Tuba, Pehlivan, Davut, Beck, Christine R., Gonzaga-Jauregui, Claudia, Muzny, Donna M., Atik, Mehmed M., Carvalho, Claudia M.B., Matur, Zeliha, Bayraktar, Serife, Boone, Philip M., Akyuz, Kaya, Gibbs, Richard A., Battaloglu, Esra, Parman, Yesim, Lupski, James R.
Έκδοση 2013Κείμενο -
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Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease από 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
Έκδοση 2022Κείμενο