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Brain : a Journal of Neurology|August 7, 2010
Neuronal networks in children with continuous spikes and waves during slow sleepMichael Siniatchkin, Kristina Groening, Jan Moehring, et al.
European Journal of Pediatrics|August 27, 2009
Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system-a novel entity?Ingo Helbig, Regina Fölster-Holst, Jochen Brasch, et al.
The Journal of Headache and Pain|April 9, 2010
MIPAS-Family-evaluation of a new multi-modal behavioral training program for pediatric headaches: clinical effects and the impact on quality of lifeWolf-Dieter Gerber, Franz Petermann, Gabriele Gerber-von Müller, et al.
Plos One|May 1, 2015
Neuronal Networks during Burst Suppression as Revealed by Source AnalysisNatia Japaridze, Muthuraman Muthuraman, Christine Reinicke, et al.
Archives of Neurology|April 5, 2012
Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiencyNorbert Brüggemann, Juliane Spiegler, Yorck Hellenbroich, et al.
Epilepsia|July 25, 2007
Hemodynamic responses to interictal epileptiform discharges in children with symptomatic epilepsyJulia Jacobs, Eliane Kobayashi, Rainer Boor, et al.
Neuropsychologia|January 14, 2014
Developmental changes of neuronal networks associated with strategic social decision-makingElisabeth Steinmann, Antonia Schmalor, Alexander Prehn-Kristensen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2018
Multifocal epilepsy in children is associated with increased long-distance functional connectivity: An explorative EEG-fMRI studyMichael Siniatchkin, Jan Moehring, Bianca Kroeher, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
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.
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