Evidence map›Paper›PMID 39933775›Full record

ArticleSaudi medical journal2025

Spectrum and classification of

Ruqayah Gy Al-Obaidi, Bassam Ms Al-Musawi

Abstract read
In one paragraph

Article in Saudi medical journal, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Clinical and Molecular Analysis ofSultan Qaboos University medical journal · 2025
    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

2 authors.

Ruqayah Gy Al-ObaidiFrom the Department of Medical Genetics (Al-Obaidi), National Center for Educational Laboratories, Medical City Campus; and from Department of Pathology and Forensic Medicine (Al-Musawi), College of Medicine, University of Baghdad, Baghdad, Iraq.
Bassam Ms Al-MusawiFrom the Department of Medical Genetics (Al-Obaidi), National Center for Educational Laboratories, Medical City Campus; and from Department of Pathology and Forensic Medicine (Al-Musawi), College of Medicine, University of Baghdad, Baghdad, Iraq.ORCID https://orcid.org/0000-0002-4404-377X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo study the spectrum and classification of

methodsFifty-five unrelated children with a clinical diagnosis of Wilson disease (WD) were recruited. Deoxyribonucleic acid was extracted from peripheral blood samples, and variants in the

resultsSeventy-six deleterious variants were detected in 97 out of 110 alleles of the

conclusionThe mutational spectrum of

Indexed as

Copper-Transporting ATPasesHepatolenticular DegenerationAdolescentAllelesChildChild, PreschoolFemaleHumansIraqMaleMutationATP7B protein, humanCopper-Transporting ATPasesATP7Bc.3305T>Cc.956delCchildrenIraqNext-Generation SequencingWilson disease

Identifiers

PMID39933775
PMCPMC11822923

What OpenQuestion holds

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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.