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Journal of Child Neurology|January 8, 2011
The homozygous ganglioside-induced differentiation-associated protein 1 mutation c.373C > T causes a very early-onset neuropathy: case report and literature reviewCarlo Fusco, Valentina Ucchino, Giovanni Barbon, et al.Journal of Child Neurology|January 8, 2011
Intracardiac shunting and stroke in children: a systematic reviewMichael M Dowling, Catherine M IkembaJournal of Child Neurology|January 8, 2011
Lymphocytic hypophysitis in children: a novel presentation and literature reviewArun A Kalra, Rosario Maria S Riel-Romero, Eduardo Gonzalez-ToledoJournal of Child Neurology|July 13, 2011
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: compound heterozygotes for nonsense mutations of the SACS geneVinodh Narayanan, Stephen G Rice, Shannon S Olfers, et al.Journal of Child Neurology|July 22, 2011
Maltreatment of children with disabilities: the breaking pointNancy MurphyJournal of Child Neurology|October 18, 2007
Pediatric headache: an examination of process variables in treatmentJamie A Cvengros, Dennis Harper, Michael ShevellJournal of Child Neurology|October 18, 2007
Neurological examination of difficult and poorly cooperative childrenMohammed M S JanJournal of Child Neurology|October 18, 2007
Benign hereditary chorea: clinical, neuroimaging, and genetic findingsMuhammad Mahajnah, Dov Inbar, Adam Steinmetz, et al.Journal of Child Neurology|September 1, 2007
Perspectives on clinical trials in spinal muscular atrophyKathryn J Swoboda, John T Kissel, Thomas O Crawford, et al.Journal of Child Neurology|September 1, 2007
Modern management of spinal muscular atrophySusan T IannacconePageof 586