Evidence map›Paper›PMID 40137425›Full record

ArticleJournal of personalized medicine2025

Clinical Outcomes and Genetic Mutations in Turkish Patients with Type 1 Gaucher Disease: Insights from a Single-Center Study.

Ali R Çalışkan, Jasmin Weninger, Huseyin Kaçmaz, Eda Nacar, Emine Şahin Kutlu, Hüseyin Onay, Süleyman Bayram, Ali Canbay, Mustafa K Özcürümez

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of personalized medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

9 authors.

Ali R ÇalışkanDepartment of Gastroenterology, Faculty of Medicine, Adiyaman University, 02100 Adiyaman, Turkey.ORCID 0000-0003-3187-8548
Jasmin WeningerDepartment of Medicine, Knappschaft Kliniken Universitätsklinikum Bochum, Ruhr University, 44892 Bochum, Germany.ORCID 0009-0008-7116-8931
Huseyin KaçmazDepartment of Gastroenterology, Faculty of Medicine, Adiyaman University, 02100 Adiyaman, Turkey.ORCID 0000-0001-6788-3459
Eda NacarDepartment of Internal Medicine, Faculty of Medicine, Adiyaman University, 02100 Adiyaman, Turkey.
Emine Şahin KutluDepartment of Internal Medicine, Faculty of Medicine, Adiyaman University, 02100 Adiyaman, Turkey.
Hüseyin OnayDepartment of Genetics, Multigen Genetic Diseases Center, 35535 Izmir, Turkey.
Süleyman BayramDepartment of Public Health Nursing, Faculty of Health Sciences, Adıyaman University, 02040 Adıyaman, Turkey.
Ali CanbayDepartment of Medicine, Knappschaft Kliniken Universitätsklinikum Bochum, Ruhr University, 44892 Bochum, Germany.
Mustafa K ÖzcürümezDepartment of Medicine, Knappschaft Kliniken Universitätsklinikum Bochum, Ruhr University, 44892 Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

enzyme replacement therapygaucher diseaseGBA1-mutationglucocerebrosidaselysosomal storage disease

Identifiers

PMID40137425
PMCPMC11943071

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.