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Migraine, Familial Hemiplegic, 3

Known as: FHM3 
National Institutes of Health

Papers overview

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2019
2019
BackgroundFamilial hemiplegic migraine (FHM) is a group of genetic migraine, associated with hemiparesis and aura. Three… 
2018
2018
Familial hemiplegic migraine (FHM) is a rare, monogenic, autosomal dominant subtype of migraine, in which three genes, CACNA1A… 
Review
2014
Review
2014
Since the last RCPA Pathology Update meeting, NATA is receiving an ever increasing number of requests to have next generation… 
Review
2010
Review
2010
Chronic pain often represents a severe, debilitating condition. Up to 10% of the worldwide population are affected, and many… 
Review
2008
Review
2008
Purpose of reviewTo highlight recent genetic findings in migraine and discuss, new mutations in hemiplegic migraine genes in… 
Review
2008
Review
2008
Migraine is a multifactorial disorder in which both multiple genetic (estimated at up to 61%) and non-genetic factors are… 
Review
2006
Review
2006
ZusammenfassungZwillings- und Familienstudien belegen die Bedeutung genetischer Faktoren für die Migräne, insbesondere die Migr… 
2006
2006
Migraine is a frequent primary paroxysmal headache disorder. Within the migraine spectrum, rare variants can be recognized, such… 
Review
2006
Review
2006
Twin and family studies provide evidence of a genetic component in migraine, in particular migraine with aura (MA). Familial…