(Q24672636)

1

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Y Hahn

2

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E H Sohn

3

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Y J Lee

4

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J H Yun

5

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J M Kim

6

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J H Chung

Journal of Neurology, Neurosurgery and Psychiatry

7

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language of work or name

English

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publication date

May 2001

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published in

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volume

70

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issue

5

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page(s)

618-23

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cites work

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Genomic organization of the human skeletal muscle sodium channel gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Assignment of a human skeletal muscle sodium channel α-subunit gene (SCN4A) to 17q23.1–25.3

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Primary structure of the adult human skeletal muscle voltage‐dependent sodium channel

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Ion-channel defects and aberrant excitability in myotonia and periodic paralysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

The skeletal muscle sodium and chloride channel diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737343

Mutations of sodium channels in periodic paralysis: can they explain the disease and predict treatment?

28 September 2017

1 reference

12 December 2020

Lack of sodium channel mutation in an Italian family with paramyotonia congenita

1 reference

12 December 2020

Adynamia episodica and paralysis periodica paramyotonica

1 reference

12 December 2020

Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families

1 reference

12 December 2020

Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapy

1 reference

12 December 2020

Myotonia fluctuans. A third type of muscle sodium channel disease

1 reference

12 December 2020