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Epilepsia
|
January 7, 2020
SCN2A channelopathies: Mechanisms and models
Ulrike B S Hedrich, Stephan Lauxmann, Holger Lerche
Epilepsia
|
May 16, 2008
A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1
Yvonne G Weber, Miriam Jacob, Gabriele Weber, et al.
Pflugers Archiv : European Journal of Physiology
|
April 20, 2010
KV7 channelopathies
Snezana Maljevic, Thomas V Wuttke, Guiscard Seebohm, et al.
Advances in Experimental Medicine and Biology
|
September 9, 2010
Hereditary channelopathies in neurology
Karin Jurkat-Rott, Holger Lerche, Yvonne Weber, et al.
Epilepsy Research
|
March 10, 2009
Cervical spinal MRI in a patient with a vagus nerve stimulator (VNS)
Robert Roebling, Klaus Huch, Jan Kassubek, et al.
Neurological Research and Practice
|
December 16, 2020
Neuro-Sweet syndrome - a rare differential diagnosis in aseptic meningoencephalitis
Elgin Hoffmann, Christian Boßelmann, Stephan Forchhammer, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 26, 2014
Genetic biomarkers in epilepsy
Yvonne G Weber, Anne T Nies, Matthias Schwab, et al.
Pediatric Neurology
|
July 9, 2013
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine
Iciar Sánchez-Albisua, Martin Schöning, Karin Jurkat-Rott, et al.
Stem Cell Research
|
August 30, 2019
Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation
Betül Uysal, Heidi Löffler, Filip Rosa, et al.
Der Nervenarzt
|
June 28, 2019
[Epileptogenesis and consequences for treatment]
Ulrike B S Hedrich, Henner Koch, Albert Becker, et al.
Page
of 29
Search research articles
Search
Showing results (31-40 of 282) with videos related to
Sort By:
Page
of 29
Epilepsia
|
January 7, 2020
SCN2A channelopathies: Mechanisms and models
Ulrike B S Hedrich, Stephan Lauxmann, Holger Lerche
Epilepsia
|
May 16, 2008
A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1
Yvonne G Weber, Miriam Jacob, Gabriele Weber, et al.
Pflugers Archiv : European Journal of Physiology
|
April 20, 2010
KV7 channelopathies
Snezana Maljevic, Thomas V Wuttke, Guiscard Seebohm, et al.
Advances in Experimental Medicine and Biology
|
September 9, 2010
Hereditary channelopathies in neurology
Karin Jurkat-Rott, Holger Lerche, Yvonne Weber, et al.
Epilepsy Research
|
March 10, 2009
Cervical spinal MRI in a patient with a vagus nerve stimulator (VNS)
Robert Roebling, Klaus Huch, Jan Kassubek, et al.
Neurological Research and Practice
|
December 16, 2020
Neuro-Sweet syndrome - a rare differential diagnosis in aseptic meningoencephalitis
Elgin Hoffmann, Christian Boßelmann, Stephan Forchhammer, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
February 26, 2014
Genetic biomarkers in epilepsy
Yvonne G Weber, Anne T Nies, Matthias Schwab, et al.
Pediatric Neurology
|
July 9, 2013
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine
Iciar Sánchez-Albisua, Martin Schöning, Karin Jurkat-Rott, et al.
Stem Cell Research
|
August 30, 2019
Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation
Betül Uysal, Heidi Löffler, Filip Rosa, et al.
Der Nervenarzt
|
June 28, 2019
[Epileptogenesis and consequences for treatment]
Ulrike B S Hedrich, Henner Koch, Albert Becker, et al.
Page
of 29