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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… Expand
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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… Expand
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Review
2011
Review
2011
GLOSSARYATPase = adenosine triphosphatase; FHM = familial hemiplegic migraine; MAP = mitogen activated protein; MS = multiple… Expand
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Review
2011
Review
2011
SummaryFamilial hemiplegic migraine (FHM) is a rare and genetically heterogeneous autosomal dominant subtype of migraine with… Expand
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Highly Cited
2010
Highly Cited
2010
Some patients with anosognosia for hemiplegia, i.e. apparent unawareness of hemiplegia, have been clinically observed to show… Expand
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2008
2008
Familial hemiplegic migraine type 2 (FHM-2) and common types of migraine show phenotypic similarities which may indicate a common… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
A1A2 Na+/K+-ATPase mutations cause familial hemiplegic migraine type 2 (FHM2). The authors identified three putative A1A2… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
Headache attacks and autonomic dysfunctions characterize migraine, a very common, disabling disorder with a prevalence of 12% in… Expand
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