Showing results (771-780 of 4,790) with videos related to
Sort By:
Pageof 479
Brain & Development|June 7, 2021
Hemiplegic migraine type 2 caused by a novel variant within the P-type ATPase motif in ATP1A2 concomitant with a CACNA1A variantTomoya Kubota, Shin Nabatame, Ruka Sato, et al.Brain & Development|June 2, 2021
A retrospective analysis of memantine use in a pediatric neurology clinicSarah Bouhadoun, Chantal Poulin, Saoussen Berrahmoune, et al.Brain & Development|January 1, 1988
Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndromeM Nakajima, S Ishii, T Mito, et al.Brain & Development|November 16, 2020
Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disabilityChupong Ittiwut, Sathida Poonmaksatit, Ponghatai Boonsimma, et al.Brain & Development|January 6, 2021
Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variantIkumi Hori, Daisuke Ieda, Shogo Ito, et al.Brain & Development|January 12, 2021
Magnetic resonance neurography in diagnosing childhood chronic inflammatory demyelinating polyradiculoneuropathyShoko Yoshii, Kazumoto Shibuya, Hajime Yokota, et al.Brain & Development|January 13, 2021
Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variantsYu Kobayashi, Jun Tohyama, Yukitoshi Takahashi, et al.Brain & Development|February 29, 2020
Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusionTomoyuki Akiyama, Soichiro Toda, Nobusuke Kimura, et al.Brain & Development|March 7, 2020
Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathyJi-Hoon Na, Saeam Shin, Donghwa Yang, et al.Brain & Development|March 9, 2020
A short form of gross motor function measure for Fukuyama congenital muscular dystrophyTakatoshi Sato, Michiru Adachi, Aya Matsuo, et al.Pageof 479