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Brain & Development|May 20, 2008
Different neuroradiological findings during two stroke-like episodes in a patient with a congenital disorder of glycosylation type IaNobutsune Ishikawa, Go Tajima, Hiroaki Ono, et al.Brain & Development|May 20, 2008
Primary soliter and multiple intracranial cyst hydatid disease: report of five casesHüseyin Per, Sefer Kumandaş, Hakan Gümüş, et al.Brain & Development|May 21, 2008
Upper limb movements and outcome in intrauterine-growth-retarded infants at 2 yearsLuba Zuk, Shaul Harel, Yael Leitner, et al.Brain & Development|May 21, 2008
Development of epilepsy in newborns with moderate hypoxic-ischemic encephalopathy and neonatal seizuresFrancesco Pisani, Manuela Orsini, Silvia Braibanti, et al.Brain & Development|January 1, 1989
Golgi study on the homozygote (Ml/Ml) of macular mutant mouseS Iwane, H Kawasaki, T Yamano, et al.Brain & Development|April 22, 2014
Carnitine in severely disabled patients: relation to anthropometric, biochemical variables, and nutritional intakeYoko Takeda, Masaru Kubota, Hinako Sato, et al.Brain & Development|January 1, 1989
Clinical improvement of adrenoleukodystrophy following intravenous gammaglobulin therapyT Miike, K Taku, T Tamura, et al.Brain & Development|January 1, 1989
Cerebral venous thrombosis associated with recurrent epilepsy-like attacksT Ichiyama, S Houdou, Y Tomita, et al.Brain & Development|January 9, 2017
Aspartylglucosaminuria caused by a novel homozygous mutation in the AGA gene was identified by an exome-first approach in a patient from JapanToshiyuki Yamamoto, Keiko Shimojima, Mayumi Matsufuji, et al.Brain & Development|January 9, 2017
Symmetrical thalamic calcification: A trio whole exome sequencing negative seriesKathleen Mary Gorman, John James Aird, Judith Conroy, et al.Pageof 483