Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy
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DOI: 10.1016/j.braindev.2019.12.007
Abstract: OBJECTIVE To understand the clinical characteristics of familial hemiplegic migraine (FHM) caused by a PRRT2 mutation and to examine the efficacy of preventive treatment. METHODS Using the literature, we investigated clinical details of FHM in… read more here.
Keywords: treatment; familial hemiplegic; prrt2 mutation; hemiplegic migraine ... See more keywords