Related references
Note: Only part of the references are listed.Pure haploinsufficiency for Dravet syndrome NaV1.1 (SCN1A) sodium channel truncating mutations
Giulia Bechi et al.
EPILEPSIA (2012)
Dravet syndrome: The long-term outcome
Pierre Genton et al.
EPILEPSIA (2011)
NaV1.1 channels and epilepsy
William A. Catterall et al.
JOURNAL OF PHYSIOLOGY-LONDON (2010)
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects
Miriam H. Meisler et al.
JOURNAL OF PHYSIOLOGY-LONDON (2010)
Dlx1&2 and Mash1 Transcription Factors Control Striatal Patterning and Differentiation Through Parallel and Overlapping Pathways
Jason E. Long et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2009)
Generation of Cre-transgenic mice using Dlx1/Dlx2 enhancers and their characterization in GABAergic interneurons
Gregory B. Potter et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2009)
Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy
John C. Oakley et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Inherited Neuronal Ion Channelopathies: New Windows on Complex Neurological Diseases
William A. Catterall et al.
JOURNAL OF NEUROSCIENCE (2008)
Reduced sodium current in Purkinje neurons from NaV1.1 mutant mice:: Implications for ataxia in severe myoclonic epilepsy in infancy
Franck Kalume et al.
JOURNAL OF NEUROSCIENCE (2007)
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons:: A circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation
Ikuo Ogiwara et al.
JOURNAL OF NEUROSCIENCE (2007)
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
Frank H. Yu et al.
NATURE NEUROSCIENCE (2006)
The origin and specification of cortical interneurons
Carl P. Wonders et al.
NATURE REVIEWS NEUROSCIENCE (2006)
Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy
I Cobos et al.
NATURE NEUROSCIENCE (2005)
Localization of voltage-gated ion channels in mammalian brain
JS Trimmer et al.
ANNUAL REVIEW OF PHYSIOLOGY (2004)
Nav 1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents
T Sugawara et al.
EPILEPSY RESEARCH (2003)
An unexpected requirement for brain-type sodium channels for control of heart rate in the mouse sinoatrial node
SKG Maier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
An unexpected role for brain-type sodium channels in coupling of cell surface depolarization to contraction in the heart
SKG Maier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Severe myoclonic epilepsy in infants - a review based on the Tokyo Women's Medical University series of 84 cases
H Oguni et al.
BRAIN & DEVELOPMENT (2001)
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
L Claes et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Sodium channel β subunits:: Anything but auxiliary
LL Isom
NEUROSCIENTIST (2001)