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Neuropadiatrie|November 1, 1977
Cranial computertomography in children with tuberous sclerosisH D Kuhlendahl, G Gross-Selbeck, H Doose, et al.
Neuropediatrics|August 1, 1993
Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp wavesW Whitehouse, U Diebold, M Rees, et al.
Neuropediatrics|August 1, 1993
Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X regionM Rees, U Diebold, K Parker, et al.
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.
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.
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