Evidence map›Paper›PMID 34046503›Full record

ArticleBioMed research international2021

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous

Jian-Hui Zhang, Dan-Dan Ruan, Ya-Nan Hu, Xing-Lin Ruan, Yao-Bin Zhu, Xiao Yang, Jia-Bin Wu, Xin-Fu Lin, Jie-Wei Luo, Fa-Qiang Tang

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Novel compound heterozygous mutation ofWorld journal of clinical cases · 2022
    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

10 authors at 1 institution in 1 country.

Jian-Hui ZhangShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0002-3053-3428
Dan-Dan RuanShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0001-9611-2979
Ya-Nan HuShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0001-6704-6108
Xing-Lin RuanDepartment of Neurology, Fujian Medical University Union Hospital, Fuzhou 350001, China.ORCID https://orcid.org/0000-0003-0074-2410
Yao-Bin ZhuDepartment of Traditional Chinese Medicine the First Affiliated Hospital, Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0003-2186-2286
Xiao YangTeaching and Research Office of Medical Cosmetology, Department of Management, Fujian Health College, Fuzhou 350001, China.ORCID https://orcid.org/0000-0003-2091-7126
Jia-Bin WuShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0002-4268-2017
Xin-Fu LinShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0002-1065-1371
Jie-Wei LuoShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0003-4271-4848
Fa-Qiang TangShengli Clinical Medical College of Fujian Medical University, Fuzhou 350001, China.ORCID https://orcid.org/0000-0002-0625-8470
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gitelman syndrome (GS) is an autosomal recessive inherited salt-losing renal tubular disease, which is caused by a pathogenic mutation of

Indexed as

MutationPedigreeAdultFemaleGenetic Predisposition to DiseaseGitelman SyndromeHashimoto DiseaseHeterozygoteHumansHypokalemiaKidney GlomerulusMagnesiumMaleMutation, MissensePhenotypeProteinuriaMagnesiumReceptors, DrugSLC12A3 protein, humanSodium Chloride SymportersSolute Carrier Family 12, Member 3thiazide receptor

Identifiers

PMID34046503
PMCPMC8128541
OpenAlexW3160436547

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.