(Q28273747)

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Normokalemic periodic paralysis is not a distinct disease

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Normokalemic periodic paralysis is not a distinct disease (English)

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normokalemic periodic paralysis

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Young-Wha Song

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Sung-Jo Kim

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Tae-Hwe Heo

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Man-Ho Kim

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June-Bum Kim

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language of work or name

English

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publication date

December 2012

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914-6

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cites work

Normokalemic periodic paralysis revisited: does it exist?

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

From mutation to myotonia in sodium channel disorders

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reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

An expanding view for the molecular basis of familial periodic paralysis

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stated in

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reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis

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reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A.

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

Novel de novo mutation in the KCNJ2 gene in a patient with Andersen-Tawil syndrome

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reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

Non-dystrophic myotonias and periodic paralyses

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stated in

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reference URL

https://api.crossref.org/works/10.1002%2FMUS.23441

retrieved

21 January 2018

Identifiers

DOI

10.1002/MUS.23441

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PubMed publication ID

22926674

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