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Annals of Neurology|August 5, 2004
The factor V G1691A mutation is a risk for porencephaly: A case-control studyOtfried M Debus, Andrea Kosch, Ronald Sträter, et al.Neuroscience Letters|October 26, 2005
P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEGBarbara J Fiedler, Otfried M Debus, Bernd A Neubauer, et al.American Journal of Medical Genetics. Part A|December 7, 2021
A mutation in the neonatal isoform of SCN2A causes neonatal-onset epilepsyAnja Penkl, Janine Reunert, Otfried M Debus, et al.Journal of Pineal Research|October 23, 2002
Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF studyOtfried M Debus, Alexander Lerchl, Hans W Bothe, et al.Neurology|July 5, 2023
Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1Kim M Thalwitzer, Jan H Driedger, Julie Xian, et al.Pageof 1