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Brain & Development|March 19, 1999
Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosisK Kurata, M Hayashi, J Satoh, et al.Brain & Development|March 19, 1999
Sturge--Weber syndrome: report of an unusual cutaneous distributionC Inan, J MarcusBrain & Development|October 24, 2000
Intranasal midazolam for prolonged convulsive seizuresN O Kutlu, C Yakinci, M Dogrul, et al.Brain & Development|October 24, 2000
Spatial cognition in children. I. Development of drawing-related (visuospatial and constructional) abilities in preschool and early school yearsE Del Giudice, D Grossi, R Angelini, et al.Brain & Development|October 24, 2000
An autopsy case of atypical adrenoleukomyeloneuropathy in childhoodM Kurihara, K Kumagai, Y Noda, et al.Brain & Development|September 14, 2000
Studies on the genotype-phenotype relation in the hph-1 mouse mutant deficient in guanosine triphosphate (GTP) cyclohydrolase I activityT Maeda, S Haeno, K Oda, et al.Brain & Development|September 14, 2000
Gene mutation in hereditary progressive dystonia with marked diurnal fluctuation (HPD), strictly defined dopa-responsive dystoniaN Nishiyama, S Yukishita, H Hagiwara, et al.Brain & Development|September 14, 2000
Autosomal recessive juvenile parkinsonismM Saito, M Maruyama, K Ikeuchi, et al.Brain & Development|September 14, 2000
Diagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiencyH Shintaku, M Asada, Y SawadaPageof 483