(Q34011949)

30 July 2017

1 reference

title

Skeletal muscle sodium current is reduced in hypokalemic periodic paralysis (English)

1 reference

hypokalemic periodic paralysis

30 July 2017

main subject

1 reference

Ruff RL

1

1 reference

30 July 2017

language of work or name

English

0 references

publication date

1 August 2000

1 reference

Proceedings of the National Academy of Sciences of the United States of America

30 July 2017

published in

1 reference

30 July 2017

volume

97

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30 July 2017

issue

18

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30 July 2017

page(s)

9832-9833

1 reference

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Voltage-gated ion channels and hereditary disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Calcium currents and transients of native and heterologously expressed mutant skeletal muscle DHP receptor alpha1 subunits (R528H)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Insulin-induced membrane changes in K(+)-depleted rat skeletal muscle.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

A calcium channel mutation causing hypokalemic periodic paralysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Interictal conduction slowing in muscle fibers in hypokalemic periodic paralysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families.

5 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Insulin modulation of ATP-sensitive K+ channel of rat skeletal muscle is impaired in the hypokalaemic state.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

A novel sodium channel mutation in a family with hypokalemic periodic paralysis

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34036

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

29 October 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

The muscle fiber conduction velocity and power spectra in familial hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Muscle fiber conduction velocity in the diagnosis of familial hypokalemic periodic paralysis--invasive versus surface determination

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Muscle fiber conduction velocity in arg1239his mutation in hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Insulin acts in hypokalemic periodic paralysis by reducing inward rectifier K+ current

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Cognitive effects of topiramate, gabapentin, and lamotrigine in healthy young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.170293197

Expression and functional characterization of the cardiac L-type calcium channel carrying a skeletal muscle DHP-receptor mutation causing hypokalaemic periodic paralysis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10954743

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.170293197

1 reference

30 July 2017

0 references

1 reference

30 July 2017

1 reference