A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G) (Q33599318)

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8 January 2020

case report

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title

A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15716625%20AND%20SRC:MED&resulttype=core&format=json

hypokalemic periodic paralysis

8 January 2020

main subject

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2

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8 January 2020

author name string

June Bum Kim

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15716625%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Jae Kyun Hur

series ordinal

3

1 reference

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8 January 2020

publication date

1 February 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15716625%20AND%20SRC:MED&resulttype=core&format=json

Journal of Korean Medical Science

8 January 2020

published in

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8 January 2020

volume

20

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8 January 2020

issue

1

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8 January 2020

page(s)

162-165

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Creative Commons Attribution-NonCommercial 3.0 Unported

8 January 2020

copyright license

start time

1 January 2005

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic Paralysis

21 June 2018

1 reference

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Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

A calcium channel mutation causing hypokalemic periodic paralysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Hypokalemic periodic paralysis exacerbated by acetazolamide

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Induction of calcium currents by the expression of the alpha 1-subunit of the dihydropyridine receptor from skeletal muscle

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Structure and function of voltage-sensitive ion channels

21 June 2018

1 reference

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Anesthetic experiences in a family with hypokalemic familial periodic paralysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Severe prognosis in a large family with hypokalemic periodic paralysis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808567

Periodic paralysis with response to spironolactone

30 October 2018

1 reference

12 December 2020

Acetazolamide opens the muscular K Ca 2+ channel: A novel mechanism of action that may explain the therapeutic effect of the drug in hypokalemic periodic paralysis

1 reference

12 December 2020

Identification of mutations including de novo mutations in Korean patients with hypokalaemic periodic paralysis

1 reference

12 December 2020

Acetazolamide treatment of hypokalemic periodic paralysis. Prevention of attacks and improvement of persistent weakness

1 reference

12 December 2020

Hypokalaemic periodic paralysis unresponsive to acetazolamide

1 reference

12 December 2020

Hypokalemic periodic paralysis with unusual responses to acetazolamide and sympathomimetics

1 reference

12 December 2020

Familial hypokalemic periodic paralysis. Clinical, diagnostic and therapeutic aspects

1 reference

12 December 2020

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

1 reference

12 December 2020

Malignant hyperthermia in a patient with hypokalemic periodic paralysis

1 reference

12 December 2020

Hypokalemic periodic paralysis mutations: confirmation of mutation and analysis of founder effect

1 reference

12 December 2020

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

1 reference

12 December 2020

10.3346/JKMS.2005.20.1.162

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15716625%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15716625%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

PubMed publication ID

15716625

1 reference