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Neuroimage|January 29, 2008
Variability of the hemodynamic response as a function of age and frequency of epileptic discharge in children with epilepsyJulia Jacobs, Colin Hawco, Eliane Kobayashi, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Epilepsia|April 30, 2009
Mapping brain activity on the verge of a photically induced generalized tonic-clonic seizureFriederike Moeller, Hartwig R Siebner, Stephan Wolff, et al.
Brain : a Journal of Neurology|November 24, 2006
Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability patternMichael Siniatchkin, Sergey Groppa, Bettina Jerosch, et al.
Epilepsy Research|June 30, 2022
Intrathecal application of ethosuximide is highly efficient in suppressing seizures in a genetic model of absence epilepsyAnna-Sophia Buschhoff, Regina Scherließ, Johanne G de Mooij-van Malsen, 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 18, 2020
SVD Square-root Iterated Extended Kalman Filter for Modeling of Epileptic Seizure Count Time Series with External InputsSidratul Moontaha, Andreas Galka, Michael Siniatchkin, et al.
Epilepsia|April 26, 2008
Simultaneous EEG-fMRI in drug-naive children with newly diagnosed absence epilepsyFriederike Moeller, Hartwig R Siebner, Stephan Wolff, et al.
Brain Topography|February 4, 2014
Cortical Thickness Changes Associated with Photoparoxysmal ResponseAlexandru Hanganu, Stanislav A Groppa, Günther Deuschl, et al.
Journal of Child Neurology|July 27, 2012
CDKL5 mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 patientsJohanna Jähn, Almuth Caliebe, Sarah von Spiczak, et al.
International Journal of Molecular Medicine|March 25, 2008
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mappingGudrun Nürnberg, Felix K Jacobi, Martina Broghammer, et al.
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