R Boor - JoVE Visualize

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Epilepsy & Behavior : E&B|May 31, 2011

Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndromeA Mueller, R Boor, G Coppola, et al.

Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 24, 2007

Combined spike-related functional MRI and multiple source analysis in the non-invasive spike localization of benign rolandic epilepsyR Boor, J Jacobs, A Hinzmann, et al.

Seizure|June 17, 2015

Intravenous levetiracetam in clinical practice--Results from an independent registryN Lang, W Esser, S Evers, et al.

Annals of Neurology|August 12, 2000

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.

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Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Epilepsy & Behavior : E&B|May 31, 2011

Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndromeA Mueller, R Boor, G Coppola, et al.

Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 24, 2007

Combined spike-related functional MRI and multiple source analysis in the non-invasive spike localization of benign rolandic epilepsyR Boor, J Jacobs, A Hinzmann, et al.

Seizure|June 17, 2015

Intravenous levetiracetam in clinical practice--Results from an independent registryN Lang, W Esser, S Evers, et al.

Annals of Neurology|August 12, 2000

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.

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