Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Search research articles

Related Experiment Videos

Central/nervous system/neuromuscularchannelopathies

¹Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK. sameer.zuberi@yorkhill.scot.nhs.UK

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society

|October 5, 2001

Summary

No abstract available in PubMed .

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

Brain : a journal of neurology·2012

Same author

Genotype-phenotype associations in SCN1A-related epilepsies.

Neurology·2011

Same author

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins.

Neurology·2010

Same author

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

Journal of medical genetics·2007

Same author

Anoxic-epileptic seizures: observational study of epileptic seizures induced by syncopes.

Archives of disease in childhood·2005

Same author

Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.

Neuropediatrics·2004