Practical aspects in the management of hypokalemic periodic paralysis (Q21245474)

Dimensions Publication ID

Dimensions

1010668446

Journal of Translational Medicine

18 August 2022

language of work or name

English

0 references

publication date

2008

0 references

published in

0 references

volume

6

0 references

issue

1

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page(s)

18

0 references

copyright license

Creative Commons Attribution 2.0 Generic

start time

21 April 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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1 reference

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

19 March 2017

1 reference

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Correlating phenotype and genotype in the periodic paralyses

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

19 March 2017

1 reference

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A novel SCN4A mutation causing myotonia aggravated by cold and potassium

19 March 2017

1 reference

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Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis

19 March 2017

1 reference

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

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SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide

12 September 2017

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Intravenous treatment of hypokalemic periodic paralysis

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Myotonia fluctuans. A third type of muscle sodium channel disease

1 reference

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