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U Stephani

Showing results (51-60 of 62) with videos related to

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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.
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.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
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.
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.
Pageof 7