Evidence map›Paper›PMID 25364683›Full record

ArticleIndian journal of endocrinology and metabolism2014

Wilson's disease: An endocrine revelation.

Nitin Kapoor, Sahana Shetty, Nihal Thomas, Thomas Vizhalil Paul

Registry-linked trialAbstract read
In one paragraph

Article in Indian journal of endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07208565 (A Cross-sectional Study of Endocrine Changes in Children With Wilson's Disease at Assiut University Children's Hospital), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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.

NCT07208565 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Cross-sectional Study of Endocrine Changes in Children With Wilson's Disease at Assiut University Children's Hospital

TypeobservationalSponsorAssiut UniversityRan2026 to 2027Enrolled30ConditionsWilson's Disease
3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Analyses ofHuman mutation · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Mutation spectrum ofMolecular genetics and metabolism reports · 2022
    Article
  10. Article
  11. Clinical presentations of Wilson disease.Annals of translational medicine · 2019
    Review
  12. Article
  13. Article
  14. 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

4 authors.

Nitin KapoorDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College and Hospital, Vellore, Tamil Nadu, India.
Sahana ShettyDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College and Hospital, Vellore, Tamil Nadu, India.
Nihal ThomasDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College and Hospital, Vellore, Tamil Nadu, India.
Thomas Vizhalil PaulDepartment of Endocrinology, Diabetes and Metabolism, Christian Medical College and Hospital, Vellore, Tamil Nadu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson's disease is an inherited disorder of copper metabolism. The affected patients, who otherwise have a near normal life span, may often suffer from some potentially treatable and under recognized endocrine disorders that may hinder their quality of life. We explored previously published literature on the various endocrine aspects of this disease with their probable underlying mechanisms, highlighting the universal need of research in this area.

Indexed as

Bone mineral densityhepatic osteodystrophyhypothyroidismrenal tubular acidosisWilson's disease

Identifiers

PMID25364683
PMCPMC4192994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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Registered trials

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.