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Noradrenergic and Cholinergic Modulation of Belief Updating
Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation
Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis
Two novel SCNIA mutations identified in families with familial hemiplegic migraine
RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice
PRRT2 MUTATION CAUSES BENIGN FAMILIAL INFANTILE CONVULSIONS
Meta-analysis of genome-wide association for migraine in six population-based European cohorts