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Neuropediatrics|November 24, 1999
Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1B Echenne, A Ducros, F Rivier, et al.
Neuropediatrics|June 1, 2000
Congenital disorder of glycosylation-Ic: case report and genetic defectF Hanefeld, C Körner, U Holzbach-Eberle, et al.
Neuropediatrics|June 1, 2000
Reorganization of the hand somatosensory cortex following perinatal unilateral brain injuryD Chu, P R Huttenlocher, D N Levin, et al.
Neuropediatrics|June 1, 2000
Novel cluster of tRNALeu(UUR) mutations in a sporadic case of infantile myopathy restricted to muscle tissueS Zanssen, M Molnar, G Buse, et al.
Neuropediatrics|June 1, 2000
Fetal-onset severe skeletal muscle glycogenosis associated with phosphorylase-b kinase deficiencyC Bührer, F van Landeghem, W Brück, et al.
Neuropediatrics|February 7, 2003
Eating epilepsy characterized by periodic spasmsC Nakazawa, S Fujimoto, M Watanabe, et al.
Neuropediatrics|February 7, 2003
Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literatureL Klinge, J Schaper, D Wieczorek, et al.
Neuropediatrics|February 7, 2003
Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literatureG Haliloglu, A Chattopadhyay, L Skorodis, et al.
Neuropediatrics|February 7, 2003
Diagnostic difficulties in childhood bilateral thalamic astrocytomasS Gudowius, V Engelbrecht, M Messing-Jünger, et al.
Neuropediatrics|October 9, 2002
Cerebellar vermis defect, oligophrenia, congenital ataxia, and hepatic fibrocirrhosis without coloboma and renal abnormalities: report of three casesG Coppola, P Vajro, S De Virgiliis, et al.
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