Evidence map›Paper›PMID 41838095›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Publisher Correction: Clinical burden, genetic heterogeneity, and diagnostic implications in primary hyperoxaluria type 2.

Seema Hashmi, Sabeeta Khatri, Habib Qaiser, Aiysha Abid, Sadaf Firasat, Sajid Sultan, Aasia Zubair, Mirza Naqi Zafar, Bashir Ahmed, Sadaf Aba Umer and 2 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Seema HashmiDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan. seemahashmi2001@gmail.com.ORCID http://orcid.org/0000-0002-5119-6248
Sabeeta KhatriDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Habib QaiserDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Aiysha AbidCenter for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Sadaf FirasatCenter for Human Genetics and Molecular Medicine, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Sajid SultanPhilip G. Ransely Department of Pediatric Urology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Aasia ZubairDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Mirza Naqi ZafarDepartment of Pathology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Bashir AhmedPhilip G. Ransely Department of Pediatric Urology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Sadaf Aba UmerPhilip G. Ransely Department of Pediatric Urology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Syed Adibul Hasan RizviDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
Irshad AliDepartment of Pediatric Nephrology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID41838095

What OpenQuestion holds

Textmetadata
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.