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No to Hattatsu = Brain and Development
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April 19, 2013
[An 8-year-old boy with anti-NMDA receptor encephalitis, successfully treated with cyclophosphamide]
Tadahiro Mitani, Yoshimitsu Ohtsuka, Kei Yamamoto, et al.
Brain & Development
|
April 29, 2019
Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutation
Ayumi Matsumoto, Masako Nagashima, Kazuhiro Iwama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 23, 2024
First evaluation of Eyberg Child Behavior Inventory for foster children in Japan
Miyuki Matano, Hisayo Katabira, Tomoe Sekine, et al.
Human Gene Therapy
|
December 1, 2020
Gene Therapy in a Mouse Model of Niemann-Pick Disease Type C1
Yoshie Kurokawa, Hitoshi Osaka, Takeshi Kouga, et al.
Brain & Development
|
November 3, 2020
Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings
Ikuko Sato-Shirai, Erika Ogawa, Atsuko Arisaka, et al.
Scientific Reports
|
May 21, 2024
Synthetic aporphine alkaloids are potential therapeutics for Leigh syndrome
Mizuki Kobayashi, Akihiko Miyauchi, Eriko F Jimbo, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
September 19, 2022
Diagnostic accuracy of a novel SARS CoV-2 rapid antigen test and usefulness of specimens collected from the anterior nasal cavity
Daisuke Tamura, Hirokazu Yamagishi, Yuji Morisawa, et al.
Molecular Genetics and Metabolism
|
March 23, 2012
Effect of curcumin in a mouse model of Pelizaeus-Merzbacher disease
Li-Hua Yu, Toshifumi Morimura, Yurika Numata, et al.
Plos One
|
August 8, 2017
Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)
Shin Hayashi, Daniela Tiaki Uehara, Kousuke Tanimoto, et al.
Journal of the Neurological Sciences
|
April 23, 2017
Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia
Mikako Enokizono, Noriko Aida, Tetsu Niwa, et al.
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Search research articles
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Showing results (101-110 of 218) with videos related to
Sort By:
Page
of 22
No to Hattatsu = Brain and Development
|
April 19, 2013
[An 8-year-old boy with anti-NMDA receptor encephalitis, successfully treated with cyclophosphamide]
Tadahiro Mitani, Yoshimitsu Ohtsuka, Kei Yamamoto, et al.
Brain & Development
|
April 29, 2019
Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutation
Ayumi Matsumoto, Masako Nagashima, Kazuhiro Iwama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
May 23, 2024
First evaluation of Eyberg Child Behavior Inventory for foster children in Japan
Miyuki Matano, Hisayo Katabira, Tomoe Sekine, et al.
Human Gene Therapy
|
December 1, 2020
Gene Therapy in a Mouse Model of Niemann-Pick Disease Type C1
Yoshie Kurokawa, Hitoshi Osaka, Takeshi Kouga, et al.
Brain & Development
|
November 3, 2020
Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings
Ikuko Sato-Shirai, Erika Ogawa, Atsuko Arisaka, et al.
Scientific Reports
|
May 21, 2024
Synthetic aporphine alkaloids are potential therapeutics for Leigh syndrome
Mizuki Kobayashi, Akihiko Miyauchi, Eriko F Jimbo, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
September 19, 2022
Diagnostic accuracy of a novel SARS CoV-2 rapid antigen test and usefulness of specimens collected from the anterior nasal cavity
Daisuke Tamura, Hirokazu Yamagishi, Yuji Morisawa, et al.
Molecular Genetics and Metabolism
|
March 23, 2012
Effect of curcumin in a mouse model of Pelizaeus-Merzbacher disease
Li-Hua Yu, Toshifumi Morimura, Yurika Numata, et al.
Plos One
|
August 8, 2017
Comprehensive investigation of CASK mutations and other genetic etiologies in 41 patients with intellectual disability and microcephaly with pontine and cerebellar hypoplasia (MICPCH)
Shin Hayashi, Daniela Tiaki Uehara, Kousuke Tanimoto, et al.
Journal of the Neurological Sciences
|
April 23, 2017
Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia
Mikako Enokizono, Noriko Aida, Tetsu Niwa, et al.
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