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Brain & Development|November 22, 2017
Duchenne muscular dystrophy with platypnea-orthodeoxia from Chilaiditi syndromeMasashi Ogasawara, Akihiko Ishiyama, Akira Sugiura, et al.Brain & Development|January 4, 2018
Prevalence of idiopathic epilepsy among school children in Gharbia Governorate, EgyptAzza Kamal Alshahawy, Amira Hamed Darwish, Safynaz Elsaid Shalaby, et al.Brain & Development|December 27, 2017
Predictive value of EEG for febrile seizure recurrenceAlberto M Cappellari, Carolina Brizio, Marta B Mazzoni, et al.Brain & Development|December 21, 2017
Different MRI-defined tuber types in tuberous sclerosis complex: Quantitative evaluation and association with disease manifestationsSimonas Jesmanas, Kristina Norvainytė, Rymantė Gleiznienė, et al.Brain & Development|March 5, 2018
A novel mutation in sphingosine-1-phosphate lyase causing congenital brain malformationDaniel Bamborschke, Matthias Pergande, Kerstin Becker, et al.Brain & Development|February 19, 2018
The hot cross bun sign in a patient with encephalitisYingyan Gan, Huici Liang, Xiaojing Li, et al.Brain & Development|March 10, 2012
Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletionHiroyuki Torisu, Akiko Iwaki, Kenzo Takeshita, et al.Brain & Development|March 10, 2012
Abnormalities of joint mobility and gait in children with autism spectrum disordersMaya Shetreat-Klein, Shlomo Shinnar, Isabelle RapinBrain & Development|January 1, 1990
Glucose, free fatty acid and ketone body metabolism in Duchenne muscular dystrophyH Nishio, H Wada, T Matsuo, et al.Brain & Development|January 1, 1990
Ocular manifestations in Fukuyama type congenital muscular dystrophyM Yoshioka, S Kuroki, T KondoPageof 480