Comparison of Predictive Values of Magnetic Resonance Biomarkers Based on Scan Timing in Neonatal Encephalopathy Following Therapeutic Hypothermia
Shibasaki, Jun, Niwa, Tetsu, Piedvache, Aurélie, Tomiyasu, Moyoko, Morisaki, Naho, Fujii, Yuta, Toyoshima, Katsuaki, Aida, Noriko
Published in The Journal of pediatrics (01.12.2021)
Published in The Journal of pediatrics (01.12.2021)
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Changes in Brain Metabolite Concentrations after Neonatal Hypoxic-ischemic Encephalopathy
Shibasaki, Jun, Aida, Noriko, Morisaki, Naho, Tomiyasu, Moyoko, Nishi, Yuri, Toyoshima, Katsuaki
Published in Radiology (01.09.2018)
Published in Radiology (01.09.2018)
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White matter microstructural changes in tuberous sclerosis: Evaluation by neurite orientation dispersion and density imaging (NODDI) and diffusion tensor images
Taoka, Toshiaki, Aida, Noriko, Fujii, Yuta, Ichikawa, Kazushi, Kawai, Hisashi, Nakane, Toshiki, Ito, Rintaro, Naganawa, Shinji
Published in Scientific reports (16.01.2020)
Published in Scientific reports (16.01.2020)
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Blended phenotype of AP4E1 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15
Murakami, Hiroaki, Uehara, Tomoko, Tsurusaki, Yoshinori, Enomoto, Yumi, Kuroda, Yukiko, Aida, Noriko, Kosaki, Kenjiro, Kurosawa, Kenji
Published in Brain & development (Tokyo. 1979) (01.03.2020)
Published in Brain & development (Tokyo. 1979) (01.03.2020)
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Clinical and neuroimaging review of monogenic cerebral small vessel disease from the prenatal to adolescent developmental stage
Enokizono, Mikako, Kurokawa, Ryo, Yagishita, Akira, Nakata, Yasuhiro, Koyasu, Sho, Nihira, Hiroshi, Kuwashima, Shigeko, Aida, Noriko, Kono, Tatsuo, Mori, Harushi
Published in Japanese journal of radiology (01.02.2024)
Published in Japanese journal of radiology (01.02.2024)
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Neuroimaging findings of inborn errors of metabolism: urea cycle disorders, aminoacidopathies, and organic acidopathies
Enokizono, Mikako, Aida, Noriko, Yagishita, Akira, Nakata, Yasuhiro, Ideguchi, Reiko, Kurokawa, Ryo, Kono, Tatsuo, Moritani, Toshio, Mori, Harushi
Published in Japanese journal of radiology (01.07.2023)
Published in Japanese journal of radiology (01.07.2023)
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A small pons as a characteristic finding in Down syndrome: A quantitative MRI study
Fujii, Yuta, Aida, Noriko, Niwa, Tetsu, Enokizono, Mikako, Nozawa, Kumiko, Inoue, Tomio
Published in Brain & development (Tokyo. 1979) (01.04.2017)
Published in Brain & development (Tokyo. 1979) (01.04.2017)
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Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood
Ohba, Chihiro, Osaka, Hitoshi, Iai, Mizue, Yamashita, Sumimasa, Suzuki, Yume, Aida, Noriko, Shimozawa, Nobuyuki, Takamura, Ayumi, Doi, Hiroshi, Tomita-Katsumoto, Atsuko, Nishiyama, Kiyomi, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Eto, Yoshikatsu, Tanaka, Fumiaki, Matsumoto, Naomichi, Saitsu, Hirotomo
Published in Neurogenetics (01.11.2013)
Published in Neurogenetics (01.11.2013)
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Expanding the phenotype of COL4A1-related disorders—Four novel variants
Nishimura, Naoto, Kumaki, Tatsuro, Murakami, Hiroaki, Enomoto, Yumi, Tsurusaki, Yoshinori, Tsuji, Megumi, Tsuyusaki, Yu, Goto, Tomohide, Aida, Noriko, Kurosawa, Kenji
Published in Brain & development (Tokyo. 1979) (01.10.2020)
Published in Brain & development (Tokyo. 1979) (01.10.2020)
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WDR45 mutations in three male patients with West syndrome
Nakashima, Mitsuko, Takano, Kyoko, Tsuyusaki, Yu, Yoshitomi, Shinsaku, Shimono, Masayuki, Aoki, Yoshihiro, Kato, Mitsuhiro, Aida, Noriko, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Osaka, Hitoshi, Saitsu, Hirotomo, Matsumoto, Naomichi
Published in Journal of human genetics (01.07.2016)
Published in Journal of human genetics (01.07.2016)
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Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis
Enomoto, Yumi, Tsurusaki, Yoshinori, Harada, Noriaki, Aida, Noriko, Kurosawa, Kenji
Published in Congenital anomalies (01.07.2018)
Published in Congenital anomalies (01.07.2018)
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Influence of ADORA2A gene polymorphism on leukoencephalopathy risk in MTX-treated pediatric patients affected by hematological malignancies
Tsujimoto, Shin-ichi, Yanagimachi, Masakatsu, Tanoshima, Reo, Urayama, Kevin Y., Tanaka, Fumiko, Aida, Noriko, Goto, Hiroaki, Ito, Shuichi
Published in Pediatric blood & cancer (01.11.2016)
Published in Pediatric blood & cancer (01.11.2016)
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Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy
Kodera, Hirofumi, Osaka, Hitoshi, Iai, Mizue, Aida, Noriko, Yamashita, Akio, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi
Published in Journal of human genetics (01.02.2015)
Published in Journal of human genetics (01.02.2015)
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Elevation of neuron specific enolase and brain iron deposition on susceptibility-weighted imaging as diagnostic clues for beta-propeller protein-associated neurodegeneration in early childhood: Additional case report and review of the literature
Takano, Kyoko, Shiba, Naoko, Wakui, Keiko, Yamaguchi, Tomomi, Aida, Noriko, Inaba, Yuji, Fukushima, Yoshimitsu, Kosho, Tomoki
Published in American journal of medical genetics. Part A (01.02.2016)
Published in American journal of medical genetics. Part A (01.02.2016)
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