van Egmond, Martje E <br/><br/>
Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment.  [electronic resource] 

 -  European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society  Nov 2015 
 - 726-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1532-2130 
<br/><br/><label>Standard No.: </label>10.1016/j.ejpn.2015.07.003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anticonvulsants--therapeutic use<br/>Ataxia Telangiectasia--etiology<br/>Brain Diseases--complications<br/>Child<br/>Coffin-Lowry Syndrome--etiology<br/>Early Diagnosis<br/>Electromyography<br/>Epilepsies, Myoclonic--genetics<br/>Epilepsy--etiology<br/>Female<br/>Humans<br/>Male<br/>Movement Disorders--etiology<br/>Myoclonus--drug therapy<br/>NAV1.1 Voltage-Gated Sodium Channel--genetics<br/>Nervous System Diseases--complications<br/>Young Adult