Familial Hemiplegic Migraine

Known as: Familial Hemiplegic Migraines, Hemiplegic Migraine, Familial, Hemiplegic-Ophthalmoplegic Migraine 
A migraine disorder characterized by individual and family history of aura that includes motor weakness.
National Institutes of Health

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Highly Cited
2003
Highly Cited
2003
Familial hemiplegic migraine (FHM) is a rare, severe, autosomal dominant subtype of migraine with aura. Up to 75% of FHM families… (More)
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Highly Cited
2002
Highly Cited
2002
Familial hemiplegic migraine (FHM) is a rare autosomal dominantly inherited subtype of migraine with aura. The clinical… (More)
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Highly Cited
2001
Highly Cited
2001
Trivial head trauma may be complicated by severe, sometimes even fatal, cerebral edema and coma occurring after a lucid interval… (More)
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Highly Cited
1999
Highly Cited
1999
Mutations in alpha1A, the pore-forming subunit of P/Q-type calcium channels, are linked to several human diseases, including… (More)
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Highly Cited
1999
Highly Cited
1999
OBJECTIVE To search for mutations in the calcium channel gene CACNA1A and to study the genotype-phenotype correlation in a family… (More)
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Highly Cited
1997
Highly Cited
1997
Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped an FHM gene on… (More)
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Highly Cited
1996
Highly Cited
1996
Genes for familial hemiplegic migraine (FHM) and episodic ataxia type-2 (EA-2) have been mapped to chromosome 19p13. We… (More)
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1996
1996
Familial hemiplegic migraine (FHM) is an autosomal dominant disorder characterized by transient hemiplegia during the aura phase… (More)
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Highly Cited
1994
Highly Cited
1994
Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped a gene… (More)
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Highly Cited
1993
Highly Cited
1993
Familial hemiplegic migraine is an autosomal dominant disorder of unknown pathogenesis in which the migrainous attacks are marked… (More)
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