Hemiplegic migraine: genetics and pathophysiology. [PDF]
Pietrobon D.
europepmc +1 more source
Clinical and genetic analysis of PRRT2 gene mutations in a cohort of 21 pediatric patients: a case series. [PDF]
Zheng X, Lin C.
europepmc +1 more source
The emerging role of the meningeal lymphatic and glymphatic systems in migraine pathophysiology: a systematic review. [PDF]
Bagheri K +7 more
europepmc +1 more source
Effectiveness and safety of anti-CGRP monoclonal antibodies in hemiplegic migraine: an individual patient quantitative analysis. [PDF]
Romozzi M +10 more
europepmc +1 more source
Hemiplegic Migraine: An Imitator of Cerebrovascular Disease. [PDF]
Kana A +4 more
europepmc +1 more source
Elicited Repetitive Daily Blindness Associated With Gain-of-Function <i>SCN1A</i> Variants and Responsiveness to Sodium Channel Blockers. [PDF]
Cestèle S +14 more
europepmc +1 more source
CACNA1A c.5610del in a three-generation family: epilepsy with ataxia/migraine. [PDF]
Long Z +6 more
europepmc +1 more source
Trigger factors for familial hemiplegic migraine
The aim was to identify and describe migraine trigger factors in patients with familial hemiplegic migraine (FHM) from a population-based ...
Jes Olesen +2 more
exaly +2 more sources
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
BACKGROUND: Familial hemiplegic migraine is an autosomal dominant severe subtype of migraine with aura characterised by some degree of hemiparesis during the attacks.
Michel D Ferrari +2 more
exaly +2 more sources

