Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Journal of Child Neurology|July 20, 2018
Predictive Value of Epileptiform Discharges for Subsequent Epilepsy After Febrile SeizuresAlja Kavčič, Zvonka Rener-PrimecThe American Journal of Case Reports|October 7, 2019
Severe Hyperkalemia Immediately After BirthAlja Kavčič, Simona Avčin, Štefan GrosekChild: Care, Health and Development|December 22, 2018
Using child- and family-centred goal setting as an outcome measure in residential rehabilitation for children and youth with acquired brain injuries: The challenge of predicting expected levels of achievementGemma Kelly, Carolyn Dunford, Rob Forsyth, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 27, 2023
Age related changes and sex related differences of functional brain networks in childhood: A high-density EEG studyAlja Kavčič, Jure Demšar, Dejan Georgiev, et al.Acta Clinica Croatica|December 11, 2019
Efficacy and tolerability of vagus nerve stimulation therapy (VNS) in Slovenian epilepsy patients: younger age and shorter duration of epilepsy might result in better outcomeAlja Kavčič, Nina Kajdič, Zvonka Rener-Primec, et al.Brain Research Bulletin|March 9, 2026
Born Under a Cloud: Neurophysiological Consequences of Maternal Smoking on Neonatal Sleep and EEG PatternsAlja Kavčič, Jure Demšar, Maša Štihec, et al.Cerebral Cortex (New York, N.Y. : 1991)|July 6, 2023
EEG functional connectivity after perinatal strokeAlja Kavčič, Jure Demšar, Dejan Georgiev, et al.Neuroimage|July 27, 2024
EEG alpha band functional brain network correlates of cognitive performance in children after perinatal strokeAlja Kavčič, Daša Kocjančič Borko, Jana Kodrič, et al.American Journal of Medical Genetics. Part A|April 22, 2026
Tubulinopathy Case Series: Marked Intrafamilial Phenotypic Variability Associated With a Novel Missense TUBB VariantAlja Kavčič, Jernej Avsenik, Karin Writzl, et al.The American Journal of Case Reports|November 5, 2022
Compound Heterozygote Mutation in the SMPD1 Gene Leading to Nieman-Pick Disease Type AAlja Kavčič, Matjaž Homan, Milanka Živanović, et al.Pageof 1