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Journal of Child Neurology|October 31, 2013
A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical patternRomina Romaniello, Claudio Zucca, Erika Tenderini, et al.Journal of Child Neurology|October 22, 2013
Detection of an atypical teratoid rhabdoid brain tumor gene deletion in circulating blood using next-generation sequencingMadhavi Chakravadhanula, Waibhav Tembe, Christophe Legendre, et al.Journal of Child Neurology|October 17, 2014
Association of genetic polymorphism of pre-microRNA-146a rs2910164 and serum high-mobility group box 1 with febrile seizures in Egyptian childrenMarianne Samir Makboul Issac, Marian Girgis, Mervat Haroun, et al.Journal of Child Neurology|August 22, 2014
Acute pseudotumoral hemicerebellitis in a child: a rare and distinct entity?Elena Alberini, Valerio Vellante, Floriana Zennaro, et al.Journal of Child Neurology|August 27, 2014
Unusual Clinical Presentation and Role of Decompressive Craniectomy in Herpes Simplex EncephalitisPratibha Singhi, Arushi Gahlot Saini, Jitendra Kumar Sahu, et al.Journal of Child Neurology|March 24, 2026
Physician Perception and Education Impact on Neurologic Treatment of People With Developmental DisabilitiesJoceline J Rodrigues, Mauricio F Villamar, Neishay Ayub, et al.Journal of Child Neurology|January 22, 2013
Vitamin D intake is inadequate in spinal muscular atrophy type I cohort: correlations with bone healthJennifer Aton, Rebecca Hurst Davis, Kristine C Jordan, et al.Journal of Child Neurology|May 23, 2026
Farber Lipogranulomatosis With Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy: Expanding the Phenotypic SpectrumLokesh Saini, Pradeep Kumar Gunasekaran, Ashna Kumar, et al.Journal of Child Neurology|May 19, 2026
Evaluating Associations Between Postconcussion Physical Activity and Brain Neurometabolite Concentrations in the Posterior Cingulate GyrusRoss Moseley, Ved Hatolkar, Mathew J Wingerson, et al.Journal of Child Neurology|May 19, 2026
Mania in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3 Disease): A Rare Neuropsychiatric Presentation in an AdolescentEkin Sut, Duygu Nur TutamPageof 586