MIGRAINE, FAMILIAL HEMIPLEGIC, 2
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Migraine is a complex brain disorder, and understanding the complexity of this prevalent disease could improve quality of life… (More)
- EMBO molecular medicine
Migraine is a common disabling brain disorder. A subtype of migraine with aura (familial hemiplegic migraine type 2: FHM2) is… (More)
To report biphasic changes in cerebral blood flow (CBF) in the acute phase of hemiplegic migraine with prolonged aura… (More)
Familial hemiplegic migraine (FHM) is a rare subtype of migraine with transient hemiplegic aura.
PATIENTS AND… (More)
- World journal of biological chemistry
Functional characterization of ATP1A2 mutations that are related to familial or sporadic hemiplegic migraine (FHM2, SHM… (More)
To report cerebral blood flow changes during attacks of hemiplegic migraine with prolonged aura (HMPA) longer than 24… (More)
- The Journal of biological chemistry
The neurological disorder familial hemiplegic migraine type II (FHM2) is caused by mutations in the α2-isoform of the Na(+),K… (More)
Familial hemiplegic migraine type 2 (FHM-2) and common types of migraine show phenotypic similarities which may indicate a common… (More)
Familial hemiplegic migraine (FHM) is a rare and genetically heterogeneous autosomal dominant subtype of migraine with aura… (More)
Headache attacks and autonomic dysfunctions characterize migraine, a very common, disabling disorder with a prevalence of 12% in… (More)