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Brain & Development|January 1, 1989
Hypoglycemia in a child with congenital muscular dystrophyS Shu, R P Cruse, G P RedmondBrain & Development|December 23, 2017
Long-term follow up of an adult with alternating hemiplegia of childhood and a p.Gly755Ser mutation in the ATP1A3 geneTomoshiro Ito, Masashi Narugami, Kiyoshi Egawa, et al.Brain & Development|December 3, 2017
Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registryMadoka Mori-Yoshimura, Yukio Mizuno, Sumiko Yoshida, et al.Brain & Development|September 21, 2017
CACNA1A-related early-onset encephalopathy with myoclonic epilepsy: A case reportTakuya Hayashida, Yoshiaki Saito, Atsushi Ishii, et al.Brain & Development|January 1, 1987
Tuberous sclerosis: aberrant metabolism of ornithine, proline and glutamate in cultured fibroblastsH Tanaka, K Nakazawa, M Arima, et al.Brain & Development|July 7, 2016
Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformationYu Kobayashi, Shinichi Magara, Kenichi Okazaki, et al.Brain & Development|July 16, 2017
The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like featuresJao-Shwann Liang, Li-Ju Lin, Ming-Tao Yang, et al.Brain & Development|January 4, 2018
Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patientsHyun Woo Kim, Zhejiu Quan, Young-Beom Kim, et al.Brain & Development|September 5, 2020
A case of severe autosomal dominant spinal muscular atrophy with lower extremity predominance caused by a de novo BICD2 mutationYuki Ueda, Takashi Suganuma, Yoko Narumi-Kishimoto, et al.Brain & Development|September 7, 2020
Dominant SCN2A mutation with variable phenotype in two generationsGouri Rao Passi, Shekeeb S MohammadPageof 483