Evidence map›Paper›PMID 29114033›Full record

ArticleThe Journal of general physiology2017

Na leak with gating pore properties in hypokalemic periodic paralysis V876E mutant muscle Ca channel.

Clarisse Fuster, Jimmy Perrot, Christine Berthier, Vincent Jacquemond, Pierre Charnet, Bruno Allard

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. A novel CACNA1S variant associated with diltiazem-related worsening of hypokalemic periodic paralysis: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  2. Periodic paralysis.Handbook of clinical neurology · 2024
    Review
  3. Article
  4. CaHandbook of experimental pharmacology · 2023
    Article
  5. Voltage-dependent CaAmerican journal of physiology. Cell physiology · 2022
    Article
  6. Article
  7. Voltage-Gated CaFrontiers in synaptic neuroscience · 2021
    Review
  8. Skeletal muscle CaPflugers Archiv : European journal of physiology · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Evaluation of mutant muscle CaThe Journal of general physiology · 2018
    Article
  13. When muscle CaThe Journal of physiology · 2018
    Review
  14. Article
  15. Stac3 enhances expression of human CaThe Journal of general physiology · 2018
    Article
  16. Review
  17. An atypical CaThe Journal of general physiology · 2017
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Clarisse FusterInstitut NeuroMyoGene, Université Lyon 1, Université de Lyon, UMR Centre National de la Recherche Scientifique 5310, Institut National de la Santé et de la Recherche Médicale U1217, Villeurbanne, France.
Jimmy PerrotInstitut NeuroMyoGene, Université Lyon 1, Université de Lyon, UMR Centre National de la Recherche Scientifique 5310, Institut National de la Santé et de la Recherche Médicale U1217, Villeurbanne, France.
Christine BerthierInstitut NeuroMyoGene, Université Lyon 1, Université de Lyon, UMR Centre National de la Recherche Scientifique 5310, Institut National de la Santé et de la Recherche Médicale U1217, Villeurbanne, France.ORCID http://orcid.org/0000-0002-9608-643X
Vincent JacquemondInstitut NeuroMyoGene, Université Lyon 1, Université de Lyon, UMR Centre National de la Recherche Scientifique 5310, Institut National de la Santé et de la Recherche Médicale U1217, Villeurbanne, France.
Pierre CharnetInstitut des Biomolécules Max Mousseron, Université Montpellier 1 et 2, UMR Centre National de la Recherche Scientifique 5247, Montpellier, France.
Bruno AllardInstitut NeuroMyoGene, Université Lyon 1, Université de Lyon, UMR Centre National de la Recherche Scientifique 5310, Institut National de la Santé et de la Recherche Médicale U1217, Villeurbanne, France bruno.allard@univ-lyon1.fr.ORCID http://orcid.org/0000-0002-7131-7828
Université Claude Bernard Lyon 1 · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 hypokalemic periodic paralysis (HypoPP1) is a poorly understood genetic neuromuscular disease characterized by episodic attacks of paralysis associated with low blood K

Indexed as

Ion Channel GatingMutation, MissenseAnimalsCaveolin 1Cells, CulturedHumansHypokalemic Periodic ParalysisMiceMuscle Fibers, SkeletalSodiumCAV1 protein, humanCaveolin 1Sodium

Identifiers

PMID29114033
PMCPMC5715907
OpenAlexW2768053464

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.