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European Journal of Medical Genetics|July 9, 2011
A 2 Mb deletion in 14q13 associated with severe developmental delay and hemophagocytic lymphohistiocytosisAlmuth Caliebe, Jose I Martin Subero, Hiltrud Muhle, et al.
Neuroimage|July 22, 2009
fMRI activation during spike and wave discharges evoked by photic stimulationFriederike Moeller, Hartwig R Siebner, Nils Ahlgrimm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 3, 2008
Childhood-onset restless legs syndrome: clinical and genetic features of 22 familiesHiltrud Muhle, Anja Neumann, Katja Lohmann-Hedrich, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 8, 2022
L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null VariantsIlona Krey, Sarah von Spiczak, Kathrine M Johannesen, et al.
Neuromolecular Medicine|June 25, 2010
Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivitySarah von Spiczak, Hiltrud Muhle, Ingo Helbig, et al.
Epilepsia Open|July 17, 2025
Efficacy and tolerability of fenfluramine with concomitant potassium bromide in patients with Dravet syndromeMilka Pringsheim, Gerhard Kluger, Adam Strzelczyk, et al.
Epilepsia|June 23, 2011
A retrospective population-based study on seizures related to childhood vaccinationSarah von Spiczak, Ingo Helbig, Ursula Drechsel-Baeuerle, et al.
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