Cited by 82Ion channel regulation and functionCardiac electrophysiology and arrhythmiasPotassium and Related Disorders

The familial periodic paralyses and nondystrophic myotonias

Ptáček, Louis·1998·The American Journal of Medicine

Integrity signals

Registry

Crossref · 10.1016/s0002-9343(98)00123-5

Cites

Statistics

Recomputing p-values needs the paper’s full text.

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Claims other papers make about this one

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  • In contrast to familial hypokalemic PP, carbonic anhydrase inhibitors have not been shown to be of benefit in thyrotoxic PP and may even increase the frequency of attacks.

    “In contrast to familial hypokalemic PP, carbonic anhydrase inhibitors have not been shown to be of benefit in thyrotoxic PP and may even increase the frequency of attacks [47].”

    From Thyrotoxic Periodic Paralysis: Clinical Challenges (2014) · cites this paper as [47]

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References 84 · Cited by 82

Authors
Ptáček, L.
Affiliations
Howard Hughes Medical Institute (US)
Corresponding author
Ptáček, Louis
Venue
The American Journal of Medicine
Publisher
Elsevier BV
Published
1998-07
Volume
105
Issue
1
Pages
58-70
ISSN
0002-9343 (ISSN-L)
OpenAlex
W2155744724
Cited by
82
References
84
Citations by year
2025: 1 · 2022: 1 · 2019: 2 · 2018: 1 · 2015: 2 · 2014: 1 · 2012: 3
FWCI
0.55
Type
journal article
Language
en
Open access
closed
Locations
  • The American Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Potassium and Related Disorders
Keywords
periodic paralysis, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, paramyotonia congenita, non-dystrophic myotonia, SCN4A mutation, autosomal dominant inheritance, genotype-phenotype correlation, temperature-sensitive mutation
MeSH terms
Humans, Ion Channels, Myotonia, Paralyses, Familial Periodic, Phenotype

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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

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