Showing results (111-120 of 129) with videos related to

Sort By:
Pageof 13
Neuropediatrics|November 9, 2000
Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndromeM Hoffmann-Riem, W Diener, C Benninger, et al.
Developmental Medicine and Child Neurology|March 22, 2003
Grip force parameters in precision grip of individuals with myelomeningoceleM Gölge, C Schütz, M Dreesmann, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Validating the effect of muscle artifact suppression in localizing focal epilepsyK G Mideksa, A Santillan-Guzman, N Japaridze, et al.
Acta Neurologica Scandinavica|June 18, 2002
Guidelines for the use of EEG methodology in the diagnosis of epilepsy. International League Against Epilepsy: commission report. Commission on European Affairs: Subcommission on European GuidelinesR Flink, B Pedersen, A B Guekht, et al.
Molecular Genetics and Metabolism|July 12, 2003
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspectsR Santer, H Muhle, T Suormala, et al.
Cephalalgia : an International Journal of Headache|August 8, 2007
Central mechanisms of controlled-release metoprolol in migraine: a double-blind, placebo-controlled studyM Siniatchkin, F Andrasik, P Kropp, et al.
Human Molecular Genetics|November 1, 1994
Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406T Martinsson, C Bjursell, H Stibler, et al.
Neuropediatrics|November 7, 2007
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander diseaseH Hartmann, J Herchenbach, U Stephani, et al.
Klinische Padiatrie|July 21, 2005
[Optimizing epilepsy therapy in children and adolescents with lamotrigine]H Siemes, U Brandl, C Helmstädter, et al.
Neuropediatrics|June 10, 2005
SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizuresK Ebach, H Joos, H Doose, et al.
Pageof 13