(Q33280531)

25 July 2017

1 reference

title

Familial hemiplegic migraine. (English)

1 reference

25 July 2017

1 reference

Daniela Pietrobon

1 reference

25 July 2017

publication date

1 April 2007

1 reference

25 July 2017

1 reference

25 July 2017

1 reference

25 July 2017

1 reference

25 July 2017

page(s)

274-284

1 reference

Neurobiology of migraine.

25 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Migraine: new molecular mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The molecular genetics of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Recent findings in headache genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Sporadic hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Structure and regulation of voltage-gated Ca2+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Physiologic principles underlying ion channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Migraine genetics: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Function and dysfunction of synaptic calcium channels: insights from mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Calcium channels and channelopathies of the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

21 January 2018

Episodic ataxia type 2.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Molecular pathogenesis of spinocerebellar ataxia type 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Suppression of cortical spreading depression in migraine prophylaxis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

New insights into migraine pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Evidence for a role of the N-methyl-D-aspartate (NMDA) receptor in cortical spreading depression in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Ion regulation in the brain: implications for pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The periaqueductal grey matter modulates trigeminovascular input: a role in migraine?

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Effects of antagonists to high-threshold calcium channels upon spinal mechanisms of pain, hyperalgesia and allodynia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Medullary N-type and P/Q-type calcium channels contribute to neuropathy-induced allodynia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Voltage-dependent calcium channels are involved in neurogenic dural vasodilatation via a presynaptic transmitter release mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Structure and mechanism of Na,K-ATPase: functional sites and their interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

ATP1A2 mutations in 11 families with familial hemiplegic migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

A novel ATP1A2 mutation in a family with FHM type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Functional roles of the alpha isoforms of the Na,K-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The Na,K-ATPase alpha 2 isoform is expressed in neurons, and its absence disrupts neuronal activity in newborn mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Malfunction of respiratory-related neuronal activity in Na+, K+-ATPase alpha2 subunit-deficient mice is attributable to abnormal Cl- homeostasis in brainstem neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Na+ pump low and high ouabain affinity alpha subunit isoforms are differently distributed in cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Na+ pump alpha 2-subunit expression modulates Ca2+ signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Sodium channel mutations in epilepsy and other neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Active properties of neuronal dendrites

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Channelopathies in idiopathic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The trigeminovascular system in humans: pathophysiologic implications for primary headache syndromes of the neural influences on the cerebral circulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Brain hyperexcitability: the basis for antiepileptic drugs in migraine prevention

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

The electrophysiology of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.NURT.2007.01.008

Minor Head Trauma–Induced Sporadic Hemiplegic Migraine Coma

21 January 2018

1 reference

12 December 2020

Haplotype-based systematic association studies of ATP1A2 in migraine with aura

1 reference

12 December 2020

Differential role of KIR channel and Na(+)/K(+)-pump in the regulation of extracellular K(+) in rat hippocampus

1 reference

12 December 2020

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

1 reference

12 December 2020

Repetitive cortical spreading depression in a gyrencephalic feline brain: inhibition by the novel benzoylamino-benzopyran SB-220453

1 reference

12 December 2020

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

1 reference

12 December 2020

Migraine, aura, and cortical spreading depression: why are we still talking about it?

1 reference

12 December 2020

Activity-dependent extracellular K+ accumulation in rat optic nerve: the role of glial and axonal Na+ pumps

1 reference

12 December 2020

Immunofluorescent localization of three Na,K-ATPase isozymes in the rat central nervous system: both neurons and glia can express more than one Na,K-ATPase

1 reference

12 December 2020

Degeneration of the amygdala/piriform cortex and enhanced fear/anxiety behaviors in sodium pump alpha2 subunit (Atp1a2)-deficient mice

1 reference

12 December 2020

P/Q-type calcium-channel blockade in the periaqueductal gray facilitates trigeminal nociception: a functional genetic link for migraine?

1 reference

12 December 2020

Glutamate uptake stimulates Na+,K+-ATPase activity in astrocytes via activation of a distinct subunit highly sensitive to ouabain.

1 reference

12 December 2020

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

1 reference

12 December 2020

Mechanisms of spreading depression and hypoxic spreading depression-like depolarization

1 reference

12 December 2020

Cortical spreading depression activates and upregulates MMP-9.

1 reference

12 December 2020

Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons.

1 reference

12 December 2020

Type I and type II Na(+) channel alpha-subunit polypeptides exhibit distinct spatial and temporal patterning, and association with auxiliary subunits in rat brain

1 reference

12 December 2020

10.1016/J.NURT.2007.01.008

Identifiers

DOI

1 reference

Dimensions Publication ID

25 July 2017

1006235466

0 references

1 reference