Hemiplegic migraine, familial type 1

Known as: FHM, MIGRAINE, FAMILIAL HEMIPLEGIC, 1, FHM1 
 
National Institutes of Health

Related topics

Related topics

14 relations
Autosomal dominant inheritanceCACNA1A geneConfusionDyscalculia
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Broader (2)

Cerebellar AtaxiaMigraine Disorders

Papers overview

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2011
2011
Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.
Familial hemiplegic migraine type 1, a monogenic migraine variant with aura, is linked to gain-of-function mutations in the… (More)
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Highly Cited
2010
Highly Cited
2010
Molecular basis of alternating access membrane transport by the sodium-hydantoin transporter Mhp1.
The structure of the sodium-benzylhydantoin transport protein Mhp1 from Microbacterium liquefaciens comprises a five-helix… (More)
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Highly Cited
2009
Highly Cited
2009
Enhanced Excitatory Transmission at Cortical Synapses as the Basis for Facilitated Spreading Depression in CaV2.1 Knockin Migraine Mice
Migraine is a common disabling brain disorder. A subtype of migraine with aura (familial hemiplegic migraine type 1: FHM1) is… (More)
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2008
2008
Divergent sodium channel defects in familial hemiplegic migraine.
Familial hemiplegic migraine type 3 (FHM3) is a severe autosomal dominant migraine disorder caused by mutations in the voltage… (More)
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Highly Cited
2007
Highly Cited
2007
Maternal family history of Alzheimer's disease predisposes to reduced brain glucose metabolism.
Having a parent affected with late-onset Alzheimer's disease (AD) is a risk factor for developing AD among cognitively normal… (More)
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Highly Cited
2006
Highly Cited
2006
Toxicity of an engineered nanoparticle (fullerene, C60) in two aquatic species, Daphnia and fathead minnow.
Water-soluble fullerene (nC60) has been shown to induce lipid peroxidation (LPO) in brain of juvenile largemouth bass (LMB… (More)
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Review
2006
Review
2006
Sporadic and familial hemiplegic migraine: diagnosis and treatment.
Hemiplegic migraine is a rare subtype of migraine with aura associated with transient hemiplegia. The weakness is caused by motor… (More)
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Highly Cited
2005
Highly Cited
2005
MHP1, a Magnaporthe grisea hydrophobin gene, is required for fungal development and plant colonization.
Fungal hydrophobins are implicated in cell morphogenesis and pathogenicity in several plant pathogenic fungi including the rice… (More)
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Highly Cited
2004
Highly Cited
2004
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.
A1A2 Na+/K+-ATPase mutations cause familial hemiplegic migraine type 2 (FHM2). The authors identified three putative A1A2… (More)
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2003
2003
Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Familial hemiplegic migraine (FHM) is a rare autosomal dominant disorder characterized by episodes of transient hemiparesis… (More)
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