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Epileptic Disorders : International Epilepsy Journal with Videotape
|
April 18, 2020
Praxis-induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome
Hirokazu Yamagishi, Masahide Goto, Hitoshi Osaka, et al.
Brain & Development
|
February 7, 2009
Expression analysis and mutation detection of DLX5 and DLX6 in autism
Naomi Nakashima, Takanori Yamagata, Masato Mori, et al.
Brain & Development
|
September 18, 2012
Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers
Yukifumi Monden, Masato Mori, Mari Kuwajima, et al.
Epilepsy & Behavior : E&B
|
May 19, 2023
Investigation of the efficacy and adverse effects of lacosamide over 36 months
Kei Wakabayashi, Hitoshi Osaka, Hirokazu Yamagishi, et al.
Journal of Human Genetics
|
August 30, 2013
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities
Ayumi Matsumoto, Mari Kuwajima, Kunio Miyake, 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.
Brain & Development
|
March 7, 2018
Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation
Akihiko Miyauchi, Hitoshi Osaka, Masako Nagashima, et al.
Brain & Development
|
February 12, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA<sup>Met</sup> gene
Mari Kuwajima, Masahide Goto, Koyuru Kurane, et al.
Brain Communications
|
August 23, 2021
Dopaminergic restoration of prefrontal cortico-putaminal network in gene therapy for aromatic l-amino acid decarboxylase deficiency
Yoshiyuki Onuki, Sayaka Ono, Takeshi Nakajima, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
August 17, 2019
Psychometric profile of the Ages and Stages Questionnaires, Japanese translation
Hidetoshi Mezawa, Sayaka Aoki, Shoji F Nakayama, et al.
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Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Epileptic Disorders : International Epilepsy Journal with Videotape
|
April 18, 2020
Praxis-induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome
Hirokazu Yamagishi, Masahide Goto, Hitoshi Osaka, et al.
Brain & Development
|
February 7, 2009
Expression analysis and mutation detection of DLX5 and DLX6 in autism
Naomi Nakashima, Takanori Yamagata, Masato Mori, et al.
Brain & Development
|
September 18, 2012
Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers
Yukifumi Monden, Masato Mori, Mari Kuwajima, et al.
Epilepsy & Behavior : E&B
|
May 19, 2023
Investigation of the efficacy and adverse effects of lacosamide over 36 months
Kei Wakabayashi, Hitoshi Osaka, Hirokazu Yamagishi, et al.
Journal of Human Genetics
|
August 30, 2013
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities
Ayumi Matsumoto, Mari Kuwajima, Kunio Miyake, 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.
Brain & Development
|
March 7, 2018
Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation
Akihiko Miyauchi, Hitoshi Osaka, Masako Nagashima, et al.
Brain & Development
|
February 12, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNA<sup>Met</sup> gene
Mari Kuwajima, Masahide Goto, Koyuru Kurane, et al.
Brain Communications
|
August 23, 2021
Dopaminergic restoration of prefrontal cortico-putaminal network in gene therapy for aromatic l-amino acid decarboxylase deficiency
Yoshiyuki Onuki, Sayaka Ono, Takeshi Nakajima, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
August 17, 2019
Psychometric profile of the Ages and Stages Questionnaires, Japanese translation
Hidetoshi Mezawa, Sayaka Aoki, Shoji F Nakayama, et al.
Page
of 2