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Brain & Development|November 9, 2021
Compound heterozygous ADAMTS9 variants in Joubert syndrome-related disorders without renal manifestationHiroko Baber Matsushita, Takuya Hiraide, Katsumi Hayakawa, et al.Brain & Development|November 10, 2021
Somatic mutations involving TSC 1 and TSC2 genes in two children with focal cortical dysplasiaRuchika Jha, Arjun Kurup, U B Kovilapu, et al.Brain & Development|March 14, 2021
Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitisMioko Mori, Tomohiro Kumada, Kenji Inoue, et al.Brain & Development|January 12, 2022
Unilateral internal carotid artery absence in trisomy 18Megumi Shiota, Keisuke Ito, Yuri Shirato, et al.Brain & Development|January 7, 2022
Long-term efficacy of low-dose perampanel for progressive myoclonus epilepsy in a patient with Gaucher disease type 3Mayu Tahara, Norimichi Higurashi, Aya Narita, et al.Brain & Development|January 19, 2022
Vitamin D and Nerve Conduction In Pediatric Type-1 Diabetes Mellitusİpek Polat, Gülay Can Yılmaz, Özge DedeoğluBrain & Development|December 5, 2021
Intravenous ketogenic diet therapy for neonatal-onset pyruvate dehydrogenase complex deficiencyTakehiko Inui, Yoichi Wada, Moriei Shibuya, et al.Brain & Development|December 8, 2021
Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorderHitomi Nishizawa, Mitsuo Motobayashi, Miwa Akahane, et al.Brain & Development|January 1, 1987
Magnetic resonance imaging of heterotopic gray matterA Ishikawa, N Fukushima, Y Wagatsuma, et al.Brain & Development|January 1, 1987
Nonspecific congenital myopathy (minimal change myopathy): a case reportY J Jong, K Shishikura, M Aoyama, et al.Pageof 482