(Q37726582)

22 August 2017

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title

Neurological channelopathies: new insights into disease mechanisms and ion channel function (English)

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22 August 2017

Dimitri M Kullmann

1

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author name string

Stephen G Waxman

series ordinal

2

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22 August 2017

language of work or name

English

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publication date

7 April 2010

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22 August 2017

published in

Journal of Physiology

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22 August 2017

volume

588

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22 August 2017

issue

Pt 11

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22 August 2017

page(s)

1823-1827

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

22 August 2017

cites work

1 reference

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1 September 2018

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Sodium channels in normal and pathological pain

1 September 2018

1 reference

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Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects

1 September 2018

1 reference

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Mutations in GABAA receptor subunits associated with genetic epilepsies

1 September 2018

1 reference

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Insights into migraine mechanisms and CaV2.1 calcium channel function from mouse models of familial hemiplegic migraine

1 September 2018

1 reference

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NaV1.1 channels and epilepsy

1 September 2018

1 reference

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Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901970

Voltage-sensor mutations in channelopathies of skeletal muscle

1 September 2018

1 reference

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1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901970

Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?

1 September 2018

1 reference

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

1 September 2018

1 reference

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Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis

1 September 2018

1 reference

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

1 September 2018

1 reference

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The self-tuning neuron: synaptic scaling of excitatory synapses

1 September 2018

1 reference

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

1 September 2018

1 reference

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

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901970

Adaptive regulation of neuronal excitability by a voltage-independent potassium conductance

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901970

Neurological Channelopathies

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20375141

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1113/JPHYSIOL.2010.190652

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22 August 2017

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1 reference