Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia.
about
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.The cerebellum and migraineA Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ InfluxDelayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraineAn epidemiological survey of hemiplegic migraineDiffusion- and perfusion-weighted MR imaging in persistent migrainous visual disturbances.Neuropsychiatric manifestations in CADASIL.Familial hemiplegic migraine.Head injury induced migraine coma simulating acute extradural intracranial haemorrhageContribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven familiesThe S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation.Management of sporadic and familial hemiplegic migraine.The genetics of migraine without aura and migraine with aura.Migraine coma.Genetic epidemiology of migraine and cluster headache.Sporadic hemiplegic migraine.Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.Plasma interleukin-1, tumour necrosis factor and hypothalamic-pituitary-adrenal axis responses during migraine attacks.Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.Stroke-Like Episodes and Cerebellar Syndrome in Phosphomannomutase Deficiency (PMM2-CDG): Evidence for Hypoglycosylation-Driven Channelopathy.Familial hemiplegic migraine: follow-up findings of diffusion-weighted magnetic resonance imaging (MRI), perfusion-MRI and [99mTc] HMPAO-SPECT in a patient with prolonged hemiplegic aura.Is familial hemiplegic migraine a hereditary form of basilar migraine?
P2860
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P2860
Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
1985年论文
@zh
1985年论文
@zh-cn
name
Migraine coma. Meningitic migr ...... al dominant cerebellar ataxia.
@en
type
label
Migraine coma. Meningitic migr ...... al dominant cerebellar ataxia.
@en
prefLabel
Migraine coma. Meningitic migr ...... al dominant cerebellar ataxia.
@en
P356
P1433
P1476
Migraine coma. Meningitic migr ...... al dominant cerebellar ataxia.
@en
P2093
Fitzsimons RB
Wolfenden WH
P304
P356
10.1093/BRAIN/108.3.555-A
P407
P478
108 ( Pt 3)
P577
1985-09-01T00:00:00Z