Evidence map›Paper›PMID 33397173›Full record

ArticleRenal failure2021

Min Li, Zhihui Yue, Hongrong Lin, Haiyan Wang, Huamu Chen, Liangzhong Sun

Open access · goldAbstract readCase Reports
In one paragraph

Article in Renal failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Coenzyme QMetabolic brain disease · 2026
    Article
  3. Review
  4. Article
  5. Prenatal Diagnosis ofKidney international reports · 2025
    Article
  6. [Research progress on monogenic inherited glomerular diseases with central nervous system symptoms].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
    Review
  7. Review
  8. The role of CoQ10 in embryonic development.Journal of assisted reproduction and genetics · 2024
    Review
  9. Primary Coenzyme Q10 Deficiency: An Update.Antioxidants (Basel, Switzerland) · 2023
    Review
  10. Review
  11. Article
  12. A novelMolecular genetics and metabolism reports · 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

6 authors at 4 institutions in 1 country.

Min LiDepartment of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhihui YueDepartment of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Hongrong LinDepartment of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Haiyan WangDepartment of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Huamu ChenDepartment of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Liangzhong SunDepartment of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Nanfang Hospital · CNSouthern Medical University · CNSun Yat-sen Memorial Hospital · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroudCoenzyme Q10 (CoQ10) is involved in the biosynthesis of adenosine triphosphate (ATP), and is most abundant in the mitochondrial membrane. The primary CoQ10 deficiency caused by

methodsClinical and pathological data and peripheral blood samples of 2 siblings with steroid-resistant nephrotic syndrome (SRNS) and their family members of a Chinese pedigree were collected. DNA was extracted and subjected to next-generation sequencing of target genes of hereditary nephropathy.

resultsCompound heterozygous mutations of

conclusionThe 2 cases harboring

Indexed as

Mitochondrial DiseasesSiblingsAlkyl and Aryl TransferasesChild, PreschoolChinaFemaleGlomerulosclerosis, Focal SegmentalHumansInfantMaleMutationNephrotic SyndromePedigreeProteinuriaUbiquinone4-hydroxybenzoate polyprenyltransferaseAlkyl and Aryl Transferasescoenzyme Q10UbiquinonechildCoQ10mitochondriamutationsteroid-resistant nephrotic syndrome

Identifiers

PMID33397173
PMCPMC7801106
OpenAlexW3120054032

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.