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Prenatal Diagnosis|June 14, 2021
Myelomeningocele-Chiari II malformation-Neurological predictability based on fetal and postnatal magnetic resonance imagingFarjad Khalaveh, Rainer Seidl, Thomas Czech, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 21, 2025
Effects of CI Electrode Pullback on Electrophysiology, Audiology, and Postoperative ImagingGina Mittmann, Philipp Mittmann, Jelena Bevanda, et al.
Brain and Language|July 9, 2016
Intrafamilial phenotypic variability of Specific Language ImpairmentLisa Bartha-Doering, Sabrina Regele, Dirk Deuster, et al.
European Journal of Pediatrics|December 3, 2014
MED20 mutation associated with infantile basal ganglia degeneration and brain atrophyJulia Vodopiutz, Maria T Schmook, Vassiliki Konstantopoulou, et al.
BMJ Case Reports|June 21, 2011
Isolated cytochrome c oxidase deficiency as a cause of MELASWalter Rossmanith, Michael Freilinger, Julia Roka, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 24, 2022
Sex differences in neural processing of speech in neonatesJohanna Alexopoulos, Vito Giordano, Stephan Doering, et al.
Pediatric Neurology|March 26, 2023
Humoral Immune Response Following SARS-CoV-2 mRNA Vaccination and Infection in Pediatric-Onset Multiple SclerosisMarkus Breu, Christian Lechner, Lisa Schneider, et al.
Scientific Reports|February 13, 2020
A novel de novo variant of GABRA1 causes increased sensitivity for GABA in vitroFriederike Steudle, Sabah Rehman, Konstantina Bampali, et al.
Epilepsy Research|December 20, 2014
Efficacy and tolerability of the ketogenic diet in Dravet syndrome - Comparison with various standard antiepileptic drug regimenAnastasia Dressler, Petra Trimmel-Schwahofer, Eva Reithofer, et al.
Developmental Science|August 14, 2020
The role of the corpus callosum in language network connectivity in childrenLisa Bartha-Doering, Kathrin Kollndorfer, Ernst Schwartz, et al.
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