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MIGRAINE, FAMILIAL HEMIPLEGIC, 2

Known as: MHP2, Hemiplegic migraine, familial type 2, Familial hemiplegic migraine, type 2 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
Migraine is a complex brain disorder, and understanding the complexity of this prevalent disease could improve quality of life… 
Highly Cited
2011
Highly Cited
2011
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with aura that is caused by mutations of the… 
Review
2011
Review
2011
GLOSSARYATPase = adenosine triphosphatase; FHM = familial hemiplegic migraine; MAP = mitogen activated protein; MS = multiple… 
Review
2011
Review
2011
Highly Cited
2010
Highly Cited
2010
Some patients with anosognosia for hemiplegia, i.e. apparent unawareness of hemiplegia, have been clinically observed to show… 
Highly Cited
2008
Highly Cited
2008
Familial hemiplegic migraine type 2 (FHM-2) and common types of migraine show phenotypic similarities which may indicate a common… 
Highly Cited
2008
Highly Cited
2008
Familial hemiplegic migraine (FHM) is a rare type of migraine with aura. Mutations in three genes have been described in FHM… 
Highly Cited
2004
Highly Cited
2004
A1A2 Na+/K+-ATPase mutations cause familial hemiplegic migraine type 2 (FHM2). The authors identified three putative A1A2… 
Highly Cited
2004
Highly Cited
2004
Familial hemiplegic migraine (FHM), a rare autosomal dominant subtype of migraine with aura, has been linked to two chromosomal… 
Highly Cited
2003
Highly Cited
2003
Headache attacks and autonomic dysfunctions characterize migraine, a very common, disabling disorder with a prevalence of 12% in…