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Published in Journal of Atherosclerosis and Thrombosis (01.06.2018)
Published in Journal of Atherosclerosis and Thrombosis (01.06.2018)
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Published in Journal of Atherosclerosis and Thrombosis (01.05.2023)
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Published in Journal of human genetics (01.02.2019)
Published in Journal of human genetics (01.02.2019)
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Published in PLoS genetics (01.01.2016)
Published in PLoS genetics (01.01.2016)
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Published in Journal of human genetics (01.08.2017)
Published in Journal of human genetics (01.08.2017)
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Published in Scientific reports (27.05.2021)
Published in Scientific reports (27.05.2021)
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Published in Scientific reports (27.02.2024)
Published in Scientific reports (27.02.2024)
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Published in Journal of inherited metabolic disease (01.09.2017)
Published in Journal of inherited metabolic disease (01.09.2017)
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Published in Scientific reports (12.12.2023)
Published in Scientific reports (12.12.2023)
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Author Correction: Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan
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Published in Scientific reports (16.11.2021)
Published in Scientific reports (16.11.2021)
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Kimura, Akihiko, Mizuochi, Tatsuki, Takei, Hajime, Ohtake, Akira, Mori, Jun, Shinoda, Kunihiro, Hashimoto, Takuji, Kasahara, Mureo, Togawa, Takao, Murai, Tsuyoshi, Iida, Takashi, Nittono, Hiroshi
Published in Digestive diseases and sciences (01.11.2021)
Published in Digestive diseases and sciences (01.11.2021)
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Published in Journal of clinical pathology (01.06.2021)
Published in Journal of clinical pathology (01.06.2021)
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Published in Journal of human genetics (01.09.2023)
Published in Journal of human genetics (01.09.2023)
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Shimura, Masaru, Kuranobu, Naomi, Ogawa-Tominaga, Minako, Akiyama, Nana, Sugiyama, Yohei, Ebihara, Tomohiro, Fushimi, Takuya, Ichimoto, Keiko, Matsunaga, Ayako, Tsuruoka, Tomoko, Kishita, Yoshihito, Umetsu, Shuichiro, Inui, Ayano, Fujisawa, Tomoo, Tanikawa, Ken, Ito, Reiko, Fukuda, Akinari, Murakami, Jun, Kaji, Shunsaku, Kasahara, Mureo, Shiraki, Kazuo, Ohtake, Akira, Okazaki, Yasushi, Murayama, Kei
Published in Orphanet journal of rare diseases (24.07.2020)
Published in Orphanet journal of rare diseases (24.07.2020)
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Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan
Akiyama, Nana, Shimura, Masaru, Yamazaki, Taro, Harashima, Hiroko, Fushimi, Takuya, Tsuruoka, Tomoko, Ebihara, Tomohiro, Ichimoto, Keiko, Matsunaga, Ayako, Saito-Tsuruoka, Megumi, Yatsuka, Yukiko, Kishita, Yoshihito, Kohda, Masakazu, Namba, Akira, Kamei, Yoshimasa, Okazaki, Yasushi, Kosugi, Shinji, Ohtake, Akira, Murayama, Kei
Published in Scientific reports (11.02.2021)
Published in Scientific reports (11.02.2021)
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Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings
Sato-Shirai, Ikuko, Ogawa, Erika, Arisaka, Atsuko, Osaka, Hitoshi, Murayama, Kei, Kuwajima, Mari, Watanabe, Miyuki, Ichimoto, Keiko, Ohtake, Akira, Kumada, Satoko
Published in Brain & development (Tokyo. 1979) (01.02.2021)
Published in Brain & development (Tokyo. 1979) (01.02.2021)
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Imai-Okazaki, Atsuko, Matsunaga, Ayako, Yatsuka, Yukiko, Nitta, Kazuhiro R., Kishita, Yoshihito, Sugiura, Ayumu, Sugiyama, Yohei, Fushimi, Takuya, Shimura, Masaru, Ichimoto, Keiko, Tajika, Makiko, Ogawa-Tominaga, Minako, Ebihara, Tomohiro, Matsuhashi, Tetsuro, Tsuruoka, Tomoko, Kohda, Masakazu, Hirata, Tomoko, Harashima, Hiroko, Nojiri, Shuko, Takeda, Atsuhito, Nakaya, Akihiro, Kogaki, Shigetoyo, Sakata, Yasushi, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi
Published in International journal of cardiology (15.10.2021)
Published in International journal of cardiology (15.10.2021)
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Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis
Ebihara, Tomohiro, Nagatomo, Taro, Sugiyama, Yohei, Tsuruoka, Tomoko, Osone, Yoshiteru, Shimura, Masaru, Tajika, Makiko, Matsuhashi, Tetsuro, Ichimoto, Keiko, Matsunaga, Ayako, Akiyama, Nana, Ogawa-Tominaga, Minako, Yatsuka, Yukiko, Nitta, Kazuhiro R, Kishita, Yoshihito, Fushimi, Takuya, Imai-Okazaki, Atsuko, Ohtake, Akira, Okazaki, Yasushi, Murayama, Kei
Published in Archives of disease in childhood. Fetal and neonatal edition (01.05.2022)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.05.2022)
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A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation
Saitsu, Hirotomo, Tohyama, Jun, Walsh, Tom, Kato, Mitsuhiro, Kobayashi, Yu, Lee, Ming, Tsurusaki, Yoshinori, Miyake, Noriko, Goto, Yu-Ichi, Nishino, Ichizo, Ohtake, Akira, King, Mary-Claire, Matsumoto, Naomichi
Published in Journal of human genetics (01.10.2014)
Published in Journal of human genetics (01.10.2014)
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