Evidence map›Paper›PMID 41149783›Full record

ArticleNeurology international2025

Genetics of Frontotemporal Dementia in the Serbian Population: Findings from a Hospital-Based Cohort.

Vuk Milošević, Jelena Bašić, Marija Semnic, Eva Antić, Marina Malobabić, Milan Stoiljković

Abstract read
In one paragraph

Article in Neurology international, 2025. 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

6 authors.

Vuk MiloševićClinic of Neurology, University Clinical Center Niš, 18000 Niš, Serbia.ORCID 0000-0002-2434-8277
Jelena BašićDepartment of Biochemistry, Faculty of Medicine, University of Niš, 18000 Niš, Serbia.ORCID 0000-0002-9221-561X
Marija SemnicClinic of Neurology, University Clinical Center of Vojvodina, 21000 Novi Sad, Serbia.
Eva AntićClinic of Neurology, University Clinical Center Niš, 18000 Niš, Serbia.
Marina MalobabićClinic of Neurology, University Clinical Center Niš, 18000 Niš, Serbia.ORCID 0000-0001-5137-2793
Milan StoiljkovićDepartment of Pharmacology, Faculty of Medicine, University of Niš, 18000 Niš, Serbia.ORCID 0000-0001-7354-6846

Funding

Denali Therapeutics (United States) NCT05262023
6 · The paper itself

Abstract

BACKGROUND AND

objectivesFrontotemporal dementia (FTD) is a heterogeneous neurodegenerative disorder with autosomal dominant forms most often linked to

methodsWe studied 58 consecutive patients with FTD spectrum syndromes evaluated at a tertiary referral center. All underwent standardized neurological, neuropsychological, and imaging assessments, and family history was recorded. Genetic testing included validated assays for

resultsWomen comprised 53.45% of the cohort. The mean age was 67.88 years, with mean onset at 61.70 years. Behavioral variant FTD predominated (75.87%), while language forms were less frequent. Positive family history was present in 16 patients (27.59%). Pathogenic variants were identified in three individuals (5.17%): two unrelated carriers of the intronic

conclusionsThis first genetic study of FTD in southeastern Serbia revealed a lower mutation frequency than in Northern and Western Europe, but similar to cohorts from Southeastern Europe. The detection of

Indexed as

C9orf72frontotemporal dementiaFTLDGRNMAPTSoutheastern Europe

Identifiers

PMID41149783
PMCPMC12566824

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.