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Migraine, Familial Hemiplegic, 3

Known as: FHM3 
National Institutes of Health

Related topics

Related topics

6 relations
Autosomal dominant inheritanceHemiparesisHemiplegiaMigraine with Aura

Broader (1)

Migraine Disorders

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
What have we learned from genetic of migraine?
Review
2015
Review
2015
Clinical and Genetic Features of Familial Hemiplegic Migraine
Migraine is a common cause of episodic headache disorder, and multiple factors are associated with the pathogenic mechanism… 
Review
2014
Review
2014
The NATA/RCPA accreditation of next generation sequencing - the story so far
Since the last RCPA Pathology Update meeting, NATA is receiving an ever increasing number of requests to have next generation… 
2009
2009
Self-limited hyperexcitability: a novel pathogenic mechanism for a familial hemiplegic migraine mutation of Na v 1.1 (SCN1A) Na + channel.
Familial hemiplegic migraine (FHM) is an autosomal dominant inherited subtype of severe migraine with aura. Mutations causing FHM… 
2008
2008
Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-type Migraine and Childhood Periodic Syndromes
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes… 
2006
2006
Hemiplegic and Basilar‐type Migraine: Epidemiology, Genetics, and Mechanisms
Migraine is a frequent primary paroxysmal headache disorder. Within the migraine spectrum, rare variants can be recognized, such… 
Review
2006
Review
2006
[Genetics of migraine].
Twin and family studies provide evidence of a genetic component in migraine, in particular migraine with aura (MA). Familial… 
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