PRRT2 and hemiplegic migraine: A complex association

Neurology

Volumn 83, Issue 3, 2014, Pages 288-290

  Pelzer, Nadine ^a   De Vries, Boukje ^a   Kamphorst, Jessica T ^a   Vijfhuizen, Lisanne S ^a   Ferrari, Michel D ^a   Haan, Joost ^a,b   Van Den Maagdenberg, Arn M J M ^a   Terwindt, Gisela M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; GLUTAMINE; HEMIPLEGIA; HUMANS; MEMBRANE PROTEINS; MIGRAINE DISORDERS; NERVE TISSUE PROTEINS; PEDIGREE; PHENOTYPE; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 84905825498     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0000000000000590     Document Type: Article

References (7)

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3. Gardiner AR, Bhatia KP, Stamelou M, et al. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Neurology 2012;79: 2115-2121.
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