Evidence map›Paper›PMID 35663312›Full record

ArticleFrontiers in endocrinology2022

Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient.

Sanaa Sharari, Mustapha Aouida, Idris Mohammed, Basma Haris, Ajaz Ahmad Bhat, Iman Hawari, Sabah Nisar, Igor Pavlovski, Kabir H Biswas, Najeeb Syed and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Genes · 2024
    Article
  3. Article
  4. 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

15 authors at 2 institutions in 2 countries.

Sanaa SharariDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Mustapha AouidaDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Idris MohammedDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Basma HarisDepartment of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.
Ajaz Ahmad BhatDepartment of Research, Sidra Medicine, Doha, Qatar.
Iman HawariDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Sabah NisarDepartment of Research, Sidra Medicine, Doha, Qatar.
Igor PavlovskiDepartment of Research, Sidra Medicine, Doha, Qatar.
Kabir H BiswasDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Najeeb SyedDepartment of Research, Sidra Medicine, Doha, Qatar.
Selma MaachaDepartment of Research, Sidra Medicine, Doha, Qatar.
Jean-Charles GrivelDepartment of Research, Sidra Medicine, Doha, Qatar.
Maryam SaifaldeenDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Johan EricssonDivision of Biological and Biomedical Sciences, College of Health and Life Sciences, Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, Qatar.
Khalid HussainDepartment of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.
Qatar Foundation · QAHamad bin Khalifa University · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fanconi-Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the liver and kidney. It is inherited as an autosomal recessive disorder caused by mutations in the

Indexed as

Endocrine System DiseasesFanconi SyndromeGlucoseHEK293 CellsHomozygoteHumansMutationGlucoseclustered regularly interspaced short palindromic repeats (CRISPR)- Cas9dysglycemiaFanconi-Bickel syndrome (FBS)glucose transporter 2 (GLUT2)sodium-glucose transport protein 2 (SGLT2)

Identifiers

PMID35663312
PMCPMC9159359
OpenAlexW4280558503

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.