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Neurology|August 23, 2006
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27B A Neubauer, I Stefanova, C A Hübner, et al.
Neurology|July 16, 2008
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromesB A Neubauer, S Waldegger, J Heinzinger, et al.
Neurology|November 23, 2007
Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?K Lohmann-Hedrich, A Neumann, A Kleensang, et al.
Neurology|December 17, 1998
Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14B A Neubauer, B Fiedler, B Himmelein, et al.
Seizure|June 17, 2015
Intravenous levetiracetam in clinical practice--Results from an independent registryN Lang, W Esser, S Evers, et al.
Epilepsy Research|May 19, 2006
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsyA Ayerdi-Izquierdo, G Stavrides, J J Sellés-Martínez, et al.
Epilepsy Research|February 16, 2010
Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysisC G F de Kovel, D Pinto, U Tauer, et al.
Human Mutation|January 22, 2008
Myoclonus-dystonia: significance of large SGCE deletionsA Grünewald, A Djarmati, K Lohmann-Hedrich, et al.
Epilepsy & Behavior : E&B|March 25, 2008
The Wada test in Austrian, Dutch, German, and Swiss epilepsy centers from 2000 to 2005: a review of 1421 proceduresA Haag, S Knake, H M Hamer, et al.
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