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Frontiers in Neurology|May 30, 2023
Genetic and clinical features of pediatric-onset hereditary spastic paraplegia: a single-center study in JapanAzusa Ikeda, Tatsuro Kumaki, Yu Tsuyusaki, et al.Brain & Development|October 12, 2010
Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseasesMayu Shinohara, Makiko Saitoh, Jun-ichi Takanashi, et al.Biomedicines|March 29, 2023
Evaluation of Human-Induced Pluripotent Stem Cells Derived from a Patient with Schwartz-Jampel Syndrome Revealed Distinct Hyperexcitability in the Skeletal MusclesYuri Yamashita, Satoshi Nakada, Kyoko Nakamura, et al.Journal of Neurology|April 10, 2019
Correction to: A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging featuresYu Hongo, Juntaro Kaneko, Hiroki Suga, et al.Journal of Neurology|March 20, 2019
A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging featuresYu Hongo, Juntaro Kaneko, Hiroki Suga, 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 hypoplasiaMikako Enokizono, Noriko Aida, Tetsu Niwa, et al.Brain & Development|September 17, 2017
Japanese Leigh syndrome case treated with EPI-743Takeshi Kouga, Mariko Takagi, Akihiko Miyauchi, et al.Epilepsy & Behavior Reports|December 28, 2019
Epilepsy in Christianson syndrome: Two cases of Lennox-Gastaut syndrome and a review of literatureAzusa Ikeda, Ayako Yamamoto, Kazushi Ichikawa, et al.Brain & Development|September 15, 2018
Aggregate formation analysis of GFAPJanyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, et al.Brain & Development|August 25, 2020
Guidelines for the diagnosis and treatment of acute encephalopathy in childhoodMasashi Mizuguchi, Takashi Ichiyama, George Imataka, et al.Pageof 6