Evidence map›Paper›PMID 33088529›Full record

ArticleClinical case reports2020

CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis.

Nader Rezkalla, Kamran Imam, Miriam Marti, Karen Ip, Ardavan Mashhadian, Antonio Liu

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 3 institutions in 1 country.

Nader RezkallaRoss University School of Medicine Miramar Florida USA.ORCID https://orcid.org/0000-0003-4477-8300
Kamran ImamDepartment of Neurology Adventist Health White Memorial Los Angeles California USA.ORCID https://orcid.org/0000-0003-1112-815X
Miriam MartiDepartment of Neurology Adventist Health White Memorial Los Angeles California USA.
Karen IpDepartment of Neurology Adventist Health White Memorial Los Angeles California USA.
Ardavan MashhadianDepartment of Nephrology California Hospital Medical Center Los Angeles California USA.
Antonio LiuDepartment of Neurology Adventist Health White Memorial Los Angeles California USA.ORCID https://orcid.org/0000-0002-1932-7308
White Memorial Medical Center · USCalifornia Hospital Medical Center Foundation · USCalifornia Miramar University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has long been believed that the patients with thyrotoxic hypokalemic periodic paralysis (THPP) may harbor genetic mutations commonly found in familial hypokalemic periodic paralysis. Despite extensive testing, such a mutation has escaped detection until now.

Indexed as

endocrinologygeneticsmetabolic disordersneurology

Identifiers

PMID33088529
PMCPMC7562840
OpenAlexW3038278219

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.