Boys with attention-deficit/hyperactivity disorder perform wider and fewer finger tapping than typically developing boys – Peer comparisons and the effects of methylphenidate from... von Enokizono, Takashi, Ohto, Tatsuyuki, Tanaka, Mai, Maruo, Kazushi, Mizuguchi, Tomohiko, Sano, Yuko, Kandori, Akihiko, Takada, Hidetoshi

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Quantitative assessment of fine motor skills in children using magnetic sensors von Enokizono, Takashi, Ohto, Tatsuyuki, Tanaka, Mai, Maruo, Kazushi, Sano, Yuko, Kandori, Akihiko, Takada, Hidetoshi

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Novel ACOX1 mutations in two siblings with peroxisomal acyl-CoA oxidase deficiency von Morita, Atsushi, Enokizono, Takashi, Ohto, Tatsuyuki, Tanaka, Mai, Watanabe, Shiena, Takada, Yui, Iwama, Kazuhiro, Mizuguchi, Takeshi, Matsumoto, Naomichi, Morita, Masashi, Takashima, Shigeo, Shimozawa, Nobuyuki, Takada, Hidetoshi

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Schuurs‐Hoeijmakers syndrome in two patients from Japan von Hoshino, Yusuke, Enokizono, Takashi, Imagawa, Kazuo, Tanaka, Ryuta, Suzuki, Hisato, Fukushima, Hiroko, Arai, Junichi, Sumazaki, Ryo, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro

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Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles von Okamoto, Nobuhiko, Ohto, Tatsuyuki, Enokizono, Takashi, Wada, Yoshinao, Kohmoto, Tomohiro, Imoto, Issei, Haga, Yoshimi, Seino, Junichi, Suzuki, Tadashi

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Cyclic vomiting syndrome after acute autonomic and sensory neuropathy von Enokizono, Takashi, Nemoto, Kiyotaka, Fujiwara, Junko, Tanaka, Ryuta, Ohto, Tatsuyuki

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A Case of Anorexia Nervosa with Focal Cortical Dysplasia von Nemoto, Hiroki, Imagawa, Kazuo, Enokizono, Takashi, Masuda, Yosuke, Ide, Masayuki, Deguchi, Takuma, Hara, Monami, Morita, Atsushi, Kido, Takahiro, Tanaka, Mai, Ohto, Tatsuyuki, Takada, Hidetoshi

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Exonic deletions in GALC are frequent in Japanese globoid-cell leukodystrophy patients von Irahara-Miyana, Kaori, Enokizono, Takashi, Ozono, Keiichi, Sakai, Norio

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A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay von Ueno, Yuichi, Enokizono, Takashi, Fukushima, Hiroko, Ohto, Tatsuyuki, Imagawa, Kazuo, Tanaka, Mai, Sakai, Aiko, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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Novel ARX mutation identified in infantile spasm syndrome patient von Takeshita, Yohei, Ohto, Tatsuyuki, Enokizono, Takashi, Tanaka, Mai, Suzuki, Hisato, Fukushima, Hiroko, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2 von Saeki, Saki, Enokizono, Takashi, Imagawa, Kazuo, Fukushima, Hiroko, Kajikawa, Daigo, Sakai, Aiko, Tanaka, Mai, Ohto, Tatsuyuki, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kenjiro, Kosaki, Takada, Hidetoshi

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A novel BBS10 mutation identified in a patient with Bardet–Biedl syndrome with a violent emotional outbreak von Ohto, Tatsuyuki, Enokizono, Takashi, Tanaka, Ryuta, Tanaka, Mai, Suzuki, Hisato, Sakai, Aiko, Imagawa, Kazuo, Fukushima, Hiroko, Fukushima, Takashi, Sumazaki, Ryo, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro

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Continuous regional arterial infusion effective for children with acute necrotizing pancreatitis even under neutropenia von Fukushima, Hiroko, Fukushima, Takashi, Suzuki, Ryoko, Enokizono, Takashi, Matsunaga, Maki, Nakao, Tomohei, Koike, Kazutoshi, Mori, Kensaku, Matsueda, Kiyoshi, Sumazaki, Ryo

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Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia: Three Case Reports von LIANG, Qin-Chuan, OTSUKI, Taisuke, TAKAHASHI, Akio, ENOKIZONO, Takashi, KAIDO, Takanobu, KANEKO, Yuu, NAKAGAWA, Eiji, SUGAI, Kenji, SASAKI, Masayuki

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Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia von Liang, Qin-Chuan, Otsuki, Taisuke, Takahashi, Akio, Enokizono, Takashi, Kaido, Takanobu, Kaneko, Yuu, Nakagawa, Eiji, Sugai, Kenji, Sasaki, Masayuki

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Identification of a novel splice‐site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy von Nishino, Megumi, Tanaka, Mai, Imagawa, Kazuo, Yaita, Katsuyuki, Enokizono, Takashi, Ohto, Tatsuyuki, Suzuki, Hisato, Yamada, Mamiko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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Association of Kabuki syndrome and tethered cord syndrome: a report of three cases and literature review von Muroi, Ai, Enokizono, Takashi, Tsurubuchi, Takao, Tsukada, Kazuaki, Ohto, Tatsuyuki, Ishikawa, Eiichi

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Preaxial polydactyly in an individual with Wiedemann-Steiner syndrome caused by a novel nonsense mutation in KMT2A (vol 173, 2821, 2017) von Enokizono, Takashi, Ohto, Tatsuyuki, Tanaka, Ryuta, Tanaka, Mai, Suzuki, Hisato, Sakai, Aiko, Imagawa, Kazuo, Fukushima, Hiroko, Iwabuti, Atsushi, Fukushima, Takashi, Sumazaki, Ryo, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro

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Variants in KIF2A cause broad clinical presentation; the computational structural analysis of a novel variant in a patient with a cortical dysplasia, complex, with other brain malf... von Hatano, Maiko, Fukushima, Hiroko, Ohto, Tatsuyuki, Ueno, Yuichi, Saeki, Saki, Enokizono, Takashi, Tanaka, Ryuta, Tanaka, Mai, Imagawa, Kazuo, Kanai, Yu, Kato, Mitsuhiro, Shiraku, Hiroshi, Suzuki, Hisato, Uehara, Tomoko, Takenouchi, Toshiki, Kosaki, Kenjiro, Takada, Hidetoshi

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MLL2 and KDM6A mutations in patients with Kabuki syndrome von Miyake, Noriko, Koshimizu, Eriko, Okamoto, Nobuhiko, Mizuno, Seiji, Ogata, Tsutomu, Nagai, Toshiro, Kosho, Tomoki, Ohashi, Hirofumi, Kato, Mitsuhiro, Sasaki, Goro, Mabe, Hiroyo, Watanabe, Yoriko, Yoshino, Makoto, Matsuishi, Toyojiro, Takanashi, Jun-Ichi, Shotelersuk, Vorasuk, Tekin, Mustafa, Ochi, Nobuhiko, Kubota, Masaya, Ito, Naoko, Ihara, Kenji, Hara, Toshiro, Tonoki, Hidefumi, Ohta, Tohru, Saito, Kayoko, Matsuo, Mari, Urano, Mari, Enokizono, Takashi, Sato, Astushi, Tanaka, Hiroyuki, Ogawa, Atsushi, Fujita, Takako, Hiraki, Yoko, Kitanaka, Sachiko, Matsubara, Yoichi, Makita, Toshio, Taguri, Masataka, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Yoshiura, Ko-Ichiro, Matsumoto, Naomichi, Niikawa, Norio

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