Evidence map›Paper›PMID 32877990›Full record

ReviewInternational journal of molecular sciences2020

Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.

Sanaa Sharari, Mohamad Abou-Alloul, Khalid Hussain, Faiyaz Ahmad Khan

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  8. GLUT2/SLC2A2 is a bi-directional urate transporter.The Journal of biological chemistry · 2025
    Article
  9. Enhanced Bioactivity of FermentedCurrent issues in molecular biology · 2025
    Article
  10. Article
  11. Renal glucosuria in children.World journal of clinical pediatrics · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Genes · 2024
    Article
  17. Review
  18. Article
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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

4 authors at 2 institutions in 2 countries.

Sanaa SharariDivision of Biological and Biomedical Sciences, College of Health & Life Sciences, Hamad Bin Khalifa University, Qatar Foundation, Education City, Doha, Qatar.
Mohamad Abou-AlloulDepartment of Pediatric Medicine, Saida Governmental University Hospital, Beirut Arab University, Beirut 115020, Lebanon.
Khalid HussainDepartment of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.ORCID 0000-0002-5480-7112
Faiyaz Ahmad KhanDepartment of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.ORCID 0000-0003-4242-2941
Beirut Arab University · LBHamad bin Khalifa University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of glycogen in the kidney and liver is the main feature of Fanconi-Bickel Syndrome (FBS), a rare disorder of carbohydrate metabolism inherited in an autosomal recessive manner due to

Indexed as

MutationFanconi SyndromeGlucose IntoleranceGlucose Transporter Type 2HumansGlucose Transporter Type 2SLC2A2 protein, humanbirth weightcAMPdysglycaemiaFanconi–Bickel Syndrome (FBS)GLUT2 dysfunctionhepatomegalyinsulin secretionliverpancreatic β cellSLC2A2 mutation

Identifiers

PMID32877990
PMCPMC7504390
OpenAlexW3082253915

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.