Quantizing a multi-pronged open string junction von Asano, Masako, Kato, Mitsuhiro

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Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report von Sato, Rieko, Takanashi, Jun-Ichi, Tsuyusaki, Yu, Kato, Mitsuhiro, Saitsu, Hirotomo, Matsumoto, Naomichi, Takahashi, Takao

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Supersymmetric extended string field theory in NSn sector and NSn−1–R sector von Asano, Masako, Kato, Mitsuhiro

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Dopaminergic restoration of prefrontal cortico-putaminal network in gene therapy for aromatic l-amino acid decarboxylase deficiency von Onuki, Yoshiyuki, Ono, Sayaka, Nakajima, Takeshi, Kojima, Karin, Taga, Naoyuki, Ikeda, Takahiro, Kuwajima, Mari, Kurokawa, Yoshie, Kato, Mitsuhiro, Kawai, Kensuke, Osaka, Hitoshi, Sato, Toshihiko, Muramatsu, Shin-ichi, Yamagata, Takanori

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A new paradigm for West syndrome based on molecular and cell biology von Kato, Mitsuhiro

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Lissencephaly and the molecular basis of neuronal migration von Kato, Mitsuhiro, Dobyns, William B.

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Comparison of an Immunochromatographic Assay Kit with DAS-ELISA for Large-Scale Diagnosis and Molecular Discrimination of Satsuma Dwarf Virus Collected from Citrus Orchards von Kato, Mitsuhiro, Tomimura, Kenta, Ishii, Kanako

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Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation von Kobayashi, Yu, Magara, Shinichi, Okazaki, Kenichi, Komatsubara, Takao, Saitsu, Hirotomo, Matsumoto, Naomichi, Kato, Mitsuhiro, Tohyama, Jun

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Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor δ2 autoantibody von Shiihara, Takashi, Kato, Mitsuhiro, Konno, Akihiro, Takahashi, Yukitoshi, Hayasaka, Kiyoshi

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Maternal Uniparental Disomy 14 Syndrome Demonstrates Prader-Willi Syndrome-Like Phenotype von Hosoki, Kana, MS, Kagami, Masayo, MD, PhD, Tanaka, Touju, MD, PhD, Kubota, Masaya, MD, PhD, Kurosawa, Kenji, MD, PhD, Kato, Mitsuhiro, MD, PhD, Uetake, Kimiaki, MD, Tohyama, Jun, MD, PhD, Ogata, Tsutomu, MD, PhD, Saitoh, Shinji, MD, PhD

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The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome von Nakashima, Mitsuko, Miyajima, Masakazu, Sugano, Hidenori, Iimura, Yasushi, Kato, Mitsuhiro, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Arai, Hajime, Matsumoto, Naomichi

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Closed string field theory in a-gauge von Asano, Masako, Kato, Mitsuhiro

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A lattice formulation of the ${\mathcal N}=2$ supersymmetric SYK model von Kato, Mitsuhiro, Sakamoto, Makoto, So, Hiroto

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Gene therapy improves motor and mental function of aromatic l-amino acid decarboxylase deficiency von Kojima, Karin, Nakajima, Takeshi, Taga, Naoyuki, Miyauchi, Akihiko, Kato, Mitsuhiro, Matsumoto, Ayumi, Ikeda, Takahiro, Nakamura, Kazuyuki, Kubota, Tetsuo, Mizukami, Hiroaki, Ono, Sayaka, Onuki, Yoshiyuki, Sato, Toshihiko, Osaka, Hitoshi, Muramatsu, Shin-ichi, Yamagata, Takanori

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Spiky strings in de Sitter space von Kato, Mitsuhiro, Nishii, Kanji, Noumi, Toshifumi, Takeuchi, Toshiaki, Zhou, Siyi

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ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H+-ATPases is essential for brain development in humans and mice von Aoto, Kazushi, Kato, Mitsuhiro, Akita, Tenpei, Nakashima, Mitsuko, Mutoh, Hiroki, Akasaka, Noriyuki, Tohyama, Jun, Nomura, Yoshiko, Hoshino, Kyoko, Ago, Yasuhiko, Tanaka, Ryuta, Epstein, Orna, Ben-Haim, Revital, Heyman, Eli, Miyazaki, Takehiro, Belal, Hazrat, Takabayashi, Shuji, Ohba, Chihiro, Takata, Atsushi, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Fukuda, Atsuo, Matsumoto, Naomichi, Saitsu, Hirotomo

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Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review von Watanabe, Kazuki, Nakashima, Mitsuko, Kumada, Satoko, Mashimo, Hideaki, Enokizono, Mikako, Yamada, Keitaro, Kato, Mitsuhiro, Saitsu, Hirotomo

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Somatic Mutations in the MTOR gene cause focal cortical dysplasia type IIb von Nakashima, Mitsuko, Saitsu, Hirotomo, Takei, Nobuyuki, Tohyama, Jun, Kato, Mitsuhiro, Kitaura, Hiroki, Shiina, Masaaki, Shirozu, Hiroshi, Masuda, Hiroshi, Watanabe, Keisuke, Ohba, Chihiro, Tsurusaki, Yoshinori, Miyake, Noriko, Zheng, Yingjun, Sato, Tatsuhiro, Takebayashi, Hirohide, Ogata, Kazuhiro, Kameyama, Shigeki, Kakita, Akiyoshi, Matsumoto, Naomichi

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Going BAC or oligo microarray to the well: A commentary on Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental... von Kato, Mitsuhiro

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ATP1A3-related early childhood onset developmental and epileptic encephalopathy responding to corpus callosotomy: A case report von Moriyama, Kengo, Mizuno, Tomoko, Suzuki, Tomonori, Inaji, Motoki, Maehara, Taketoshi, Fujita, Atsushi, Kato, Mitsuhiro, Matsumoto, Naomichi

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