Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management (Q37860502)

24 August 2017

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title

Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management (English)

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familial hemiplegic migraine

24 August 2017

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1 reference

Anne Ducros

2

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Michael Bjørn Russell

series ordinal

1

object named as

Michael Bjørn Russell

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24 August 2017

30 March 2011

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24 August 2017

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24 August 2017

10

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24 August 2017

457-470

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24 August 2017

5

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On Recurrent Motor Paralysis in Migraine, with Report of a Family in which Recurrent Hemiplegia Accompanied the Attacks

24 August 2017

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7 January 2021

Familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial occurrence of migraine with a hemiplegic syndrome and cerebellar manifestations

1 reference

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7 January 2021

Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus

1 reference

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7 January 2021

Varieties of hemiplegic migraine

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7 January 2021

Respiratory arrest in familial hemiplegic migraine: a clinical and neuropathological study.

1 reference

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7 January 2021

An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor

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7 January 2021

Familial hemiplegic migraine: EEG and CT scan study of two cases

1 reference

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7 January 2021

Familial hemiplegic migraine--a reappraisal and a long-term follow-up study

1 reference

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7 January 2021

Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia

1 reference

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7 January 2021

Familial migraine coma: a case study

1 reference

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7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

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7 January 2021

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

1 reference

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7 January 2021

Is familial hemiplegic migraine a hereditary form of basilar migraine?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG

1 reference

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7 January 2021

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

1 reference

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7 January 2021

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

1 reference

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7 January 2021

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Acetazolamide responsiveness in familial hemiplegic migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine, nystagmus, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

No mutations in CACNA1A and ATP1A2 in probands with common types of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

1H-MRS alterations in the cerebellum of patients with familial hemiplegic migraine type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type II

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

ATP1A2 mutations in 11 families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A novel ATP1A2 mutation in a family with FHM type II

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Prolonged hemiplegic episodes in children due to mutations in ATP1A2.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Epilepsy as part of the phenotype associated with ATP1A2 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Molecular genetics of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Stepwise developmental regression associated with novel CACNA1A mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

CACNA1A Mutation Linking Hemiplegic Migraine and Alternating Hemiplegia of Childhood

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A new locus for hemiplegic migraine maps to chromosome 1q31

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine versus migraine with prolonged aura: an uncertain diagnosis in a family report.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine with irreversible brain damage.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Neurological picture. Cortical oedema: a link between delusional misidentification syndromes and hemiplegic migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A family with hemiplegic migraine and focal seizures

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine associated with an aseptic meningeal reaction

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Adult-onset hemiplegic migraine with cortical enhancement and oedema

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Serial MRI in a case of familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine during pregnancy: unusual magnetic resonance appearance with SPECT scan correlation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Prolonged cortical electrical depression and diffuse vasospasm without ischemia in a case of severe hemiplegic migraine during pregnancy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Increased risk of migraine with typical aura in probands with familial hemiplegic migraine and their relatives

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Elicited repetitive daily blindness: a new familial disorder related to migraine and epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Genetic heterogeneity of familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

An epidemiological survey of hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A long-term follow-up study of 18 patients with sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Alternating hemiplegia of childhood

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Symptomatic sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Sporadic hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial oculoleptomeningeal amyloidosis. Report of a new family with unusual features

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Implication of augmented vasogenic leakage in the mechanism of persistent aura in sporadic hemiplegic migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine with prolonged aura and multimodality imaging: a case report

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Imaging abnormalities in sporadic hemiplegic migraine on conventional MRI, diffusion and perfusion MRI and MRS.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine: hyperperfusion and abortive therapy with intravenous verapamil.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Cerebral hemodynamics in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Transcranial Doppler sonography in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Magnetic resonance angiogram evidence of vasospasm in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine with CSF abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine and its abortive therapy with intravenous verapamil

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Treatment of hemiplegic migraine with triptans

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine in childhood: diagnostic and therapeutic aspects

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Treatment of sporadic hemiplegic migraine with calcium-channel blocker verapamil

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

History of migraine with aura and cortical spreading depression from 1941 and onwards

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Divergent sodium channel defects in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Habituation of evoked responses is greater in patients with familial hemiplegic migraine than in controls: a contrast with the common forms of migraine.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Motor cortex excitability in patients with migraine with aura and hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Single-fiber EMG in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

A nosographic analysis of the migraine aura in a general population.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Characterization of consistent triggers of migraine with aura.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Hemiplegic migraine induced by exertion

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Migraine and tension-type headache in a general population: precipitating factors, female hormones, sleep pattern and relation to lifestyle.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial Hemiplegic Migraine Type 2 does not Share Hypersensitivity to Nitric Oxide with Common Types of Migraine

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Calcitonin gene-related peptide does not cause the familial hemiplegic migraine phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Familial Hemiplegic Migraine Type 1 Shows no Hypersensitivity to Nitric Oxide

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Basilar-type migraine: clinical, epidemiologic, and genetic features.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Improved Description of the Migraine Aura by a Diagnostic Aura Diary

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Timing and topography of cerebral blood flow, aura, and headache during migraine attacks

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

Lamotrigine reduces migraine aura and migraine attacks in patients with migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970048-5

7 January 2021

10.1016/S1474-4422(11)70048-5

Identifiers

DOI

1 reference

24 August 2017

1 reference

PubMed ID

21458376