Evidence map›Paper›PMID 40206416›Full record

ArticleMolecular genetics and metabolism reports2024

Borkowska Natalia, Kaluzny Lukasz, Rokicki Dariusz, Szmida Elzbieta, Kowalski Pawel, Dus-Zuchowska Monika, Skiba Pawel, Ciara Elzbieta, Biela Mateusz, Rydzanicz Malgorzata and 2 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2024. 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

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

12 authors.

Borkowska NataliaDepartment of Pediatrics SPZOZ Krotoszyn, Krotoszyn, Poland.
Kaluzny LukaszDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poland.
Rokicki DariuszDepartment of Pediatrics and Metabolic Pediatrics, Children's Memorial Health Institute, Warsaw, Poland.
Szmida ElzbietaDepartment of Genetics, Wroclaw Medical University, Wroclaw, Poland.
Kowalski PawelDepartment of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.
Dus-Zuchowska MonikaDepartment of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poland.
Skiba PawelDepartment of Genetics, Wroclaw Medical University, Wroclaw, Poland.
Ciara ElzbietaDepartment of Diagnostic Imaging, The Children's Memorial Health Institute, Warsaw, Poland.
Biela MateuszDepartment of Pediatrics, Endocrinology, Diabetology and Metabolic Diseases, Wroclaw Medical University, Wroclaw, Poland.
Rydzanicz MalgorzataDepartment of Genetics, Warsaw Medical University, Warsaw, Poland.
Ploski RafalDepartment of Genetics, Warsaw Medical University, Warsaw, Poland.
Smigiel RobertDepartment of Pediatrics, Endocrinology, Diabetology and Metabolic Diseases, Wroclaw Medical University, Wroclaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ornithine transcarbamylase (OTC) deficiency is the most common urea cycle disorder. It may occur due to various changes to the

Indexed as

DuplicationHyperammonaemiaOTC deficiencyOTC gene

Identifiers

PMID40206416
PMCPMC11980696

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.