(Q38260278)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

review article

1 reference

title

Sodium channel genes in pain-related disorders: phenotype-genotype associations and recommendations for clinical use (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

8

C Geoffrey Woods

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Stephen G Waxman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Ingemar S J Merkies

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Monique M Gerrits

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Sulayman D Dib-Hajj

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

James J Cox

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

John N Wood

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Joost P H Drenth

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Catharina G Faber

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

publication date

1 November 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

page(s)

1152-1160

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

The Na(V)1.7 sodium channel: from molecule to man.

21 February 2020

cites work

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7 January 2021

Neurological perspectives on voltage-gated sodium channels.

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7 January 2021

Genetic aspects of sodium channelopathy in small fiber neuropathy

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7 January 2021

A new Nav1.7 sodium channel mutation I234T in a child with severe pain

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7 January 2021

A stop codon mutation in SCN9A causes lack of pain sensation

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7 January 2021

Voltage-gated sodium channel polymorphisms play a pivotal role in the development of oxaliplatin-induced peripheral neurotoxicity: results from a prospective multicenter study

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7 January 2021

Genetic polymorphisms of SCN10A are associated with functional dyspepsia in Japanese subjects.

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7 January 2021

Genetic variation in SCN10A influences cardiac conduction

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7 January 2021

Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade

1 reference

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7 January 2021

Mutations at opposite ends of the DIII/S4-S5 linker of sodium channel Na V 1.7 produce distinct pain disorders

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7 January 2021

Deletion mutation of sodium channel Na(V)1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability.

1 reference

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7 January 2021

Mexiletine-responsive erythromelalgia due to a new Na(v)1.7 mutation showing use-dependent current fall-off.

1 reference

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7 January 2021

Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia

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7 January 2021

Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

1 reference

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7 January 2021

Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgia

1 reference

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7 January 2021

An SCN9A channelopathy causes congenital inability to experience pain

1 reference

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7 January 2021

Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations

1 reference

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7 January 2021

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons

1 reference

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7 January 2021

Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable

1 reference

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7 January 2021

Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene

1 reference

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7 January 2021

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels

1 reference

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7 January 2021

Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A sodium channel gene SCN9A polymorphism that increases nociceptor excitability

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Can robots patch-clamp as well as humans? Characterization of a novel sodium channel mutation

1 reference

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7 January 2021

Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A new Nav1.7 mutation in an erythromelalgia patient

1 reference

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7 January 2021

Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy

1 reference

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7 January 2021

Gain-of-function Nav1.8 mutations in painful neuropathy.

1 reference

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7 January 2021

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia

1 reference

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7 January 2021

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.

1 reference

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7 January 2021

Early- and late-onset inherited erythromelalgia: genotype-phenotype correlation.

1 reference

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7 January 2021

Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy.

1 reference

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7 January 2021

1 reference

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7 January 2021

The G1662S NaV1.8 mutation in small fibre neuropathy: impaired inactivation underlying DRG neuron hyperexcitability

1 reference

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7 January 2021

Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.

1 reference

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7 January 2021

Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.

1 reference

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7 January 2021

Small-fiber neuropathy Nav1.8 mutation shifts activation to hyperpolarized potentials and increases excitability of dorsal root ganglion neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.

1 reference

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7 January 2021

Size matters: Erythromelalgia mutation S241T in Nav1.7 alters channel gating

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Erythromelalgia mutation L823R shifts activation and inactivation of threshold sodium channel Nav1.7 to hyperpolarized potentials.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A de novo gain-of-function mutation in SCN11A causes loss of pain perception

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Small fibre neuropathy, fibromyalgia and dorsal root ganglia sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A case of primary erythermalgia with encephalopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Two novel mutations of SCN9A (Nav1.7) are associated with partial congenital insensitivity to pain

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A case of primary erythermalgia, wintry hypothermia and encephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Gain-of-function mutations in SCN11A cause familial episodic pain

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Autosomal dominant erythromelalgia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A single sodium channel mutation produces hyper- or hypoexcitability in different types of neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Paroxysmal extreme pain disorder mutations within the D3/S4-S5 linker of Nav1.7 cause moderate destabilization of fast inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Roles of tetrodotoxin (TTX)-sensitive Na+ current, TTX-resistant Na+ current, and Ca2+ current in the action potentials of nociceptive sensory neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Contribution of Na(v)1.8 sodium channels to action potential electrogenesis in DRG neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

NaN, a novel voltage-gated Na channel, is expressed preferentially in peripheral sensory neurons and down-regulated after axotomy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

GTP-induced tetrodotoxin-resistant Na+ current regulates excitability in mouse and rat small diameter sensory neurones

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Persistent TTX-resistant Na+ current affects resting potential and response to depolarization in simulated spinal sensory neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

GTP up-regulated persistent Na+ current and enhanced nociceptor excitability require NaV1.9.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Inactivation properties of sodium channel Nav1.8 maintain action potential amplitude in small DRG neurons in the context of depolarization

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Structural parts involved in activation and inactivation of the sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Pain perception is altered by a nucleotide polymorphism in SCN9A

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Paroxysmal itch caused by gain-of-function Nav1.7 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

Structural modelling and mutant cycle analysis predict pharmacoresponsiveness of a Na(V)1.7 mutant channel.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2814%2970150-4

7 January 2021

10.1016/S1474-4422(14)70150-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25316021%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference