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Neuropediatrics|March 19, 2009
Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in ChinaJ Yuan, H Takashima, I Higuchi, et al.Neuropediatrics|December 21, 2006
Analysis of MxA, IL-4, and IRF-1 genes in Filipino patients with subacute sclerosing panencephalitisJ R Pipo-Deveza, K Kusuhara, C L T Silao, et al.Neuropediatrics|December 21, 2006
Neurological examination at 6 to 9 months in infants with cystic periventricular leukomalaciaD Ricci, F Cowan, M Pane, et al.Neuropediatrics|August 23, 2007
Motor outcome at the age of one after perinatal hypoxic-ischemic encephalopathyP E M van Schie, J G Becher, A J Dallmeijer, et al.Neuropediatrics|August 23, 2007
Familial spinal neurofibromatosisI Pascual-Castroviejo, S-I Pascual-Pascual, R Velazquez-Fragua, et al.Neuropediatrics|November 1, 1991
Detection of optic pathway misrouting in the human albino neonateP Apkarian, P G Eckhardt, M J van SchooneveldNeuropediatrics|November 1, 1991
Acute cerebellar ataxia in a child with transient pontine lesions demonstrated by MRIR J Groen, J H Begeer, J T Wilmink, et al.Neuropediatrics|August 2, 2008
Limited knowledge of Tourette syndrome causes delay in diagnosisN M M Mol Debes, H Hjalgrim, L SkovNeuropediatrics|August 2, 2008
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutationsM Kefi, R Amouri, S Chabrak, et al.Neuropediatrics|August 2, 2008
Thought ripples on muscle waves: recognition of rippling muscle diseaseN C Voermans, N van Alfen, G Drost, et al.Pageof 255