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