Evidence map›Paper›PMID 41608521›Full record

ArticleJIMD reports2026

A Novel

Lauma Vasiļevska, Ieva Puķīte, Madara Auzenbaha, Dmitrijs Rots, Ieva Grīnfelde, Andžela Lazdāne, Sebastian Schulz-Jürgensen

Abstract read
In one paragraph

Article in JIMD reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A NovelJIMD reports · 2026
    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

7 authors.

Lauma VasiļevskaClinic of Medical Genetics and Prenatal Diagnostics Children's Clinical University Hospital Riga Latvia.ORCID https://orcid.org/0000-0002-5813-826X
Ieva PuķīteDepartment of Pediatric Gastroenterology Children's Clinical University Hospital Riga Latvia.ORCID https://orcid.org/0000-0002-3318-2555
Madara AuzenbahaClinic of Medical Genetics and Prenatal Diagnostics Children's Clinical University Hospital Riga Latvia.ORCID https://orcid.org/0000-0002-9925-2376
Dmitrijs RotsRiga Stradiņš University Riga Latvia.ORCID https://orcid.org/0000-0002-4890-9147
Ieva GrīnfeldeClinic of Medical Genetics and Prenatal Diagnostics Children's Clinical University Hospital Riga Latvia.ORCID https://orcid.org/0000-0002-1391-1220
Andžela LazdāneGenetics Laboratory Children's Clinical University Hospital Riga Latvia.
Sebastian Schulz-JürgensenDepartment of Pediatrics University Medical Center Eppendorf Hamburg Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) deficiency is a rare autosomal recessive gluconeogenesis disorder caused by variants in the

Indexed as

acute liver failurePCK1 genephosphoenolpyruvate carboxykinase deficiency

Identifiers

PMID41608521
PMCPMC12834696

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.