Evidence map›Paper›PMID 41874038›Full record

ArticleNeuroSci2026

Creutzfeldt-Jakob Disease: Spectrum of Symptoms, Clinical Progress and Diagnostics-Report of Five Cases.

Klaudia Rojewska, Natalia Dynowska, Iwona Rotter, Małgorzata Niekrasz

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PubMed Full text at PMC Publisher
In one paragraph

Article in NeuroSci, 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

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

4 authors.

Klaudia RojewskaDepartment of Neurology with Stroke Unit, Independent Public Voivodeship Combined Hospital in Szczecin, ul. Arkońska 4, 71-455 Szczecin, Poland.
Natalia DynowskaDepartment of Neurology with Stroke Unit, Independent Public Voivodeship Combined Hospital in Szczecin, ul. Arkońska 4, 71-455 Szczecin, Poland.ORCID 0009-0003-0172-7674
Iwona RotterDepartment of Medical Rehabilitation and Clinical Physiotherapy, Pomeranian Medical University in Szczecin, ul. Żołnierska 54, 71-210 Szczecin, Poland.
Małgorzata NiekraszDepartment of Neurology with Stroke Unit, Independent Public Voivodeship Combined Hospital in Szczecin, ul. Arkońska 4, 71-455 Szczecin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Creutzfeldt-Jakob disease (CJD) is a rare, fatal prion disease of the central nervous system that develops due to the conversion of the normal cellular protein PrPc to the abnormal PrPSc molecule. The first clinical cases were described in the 1920s. The aim of this paper is to present the clinical progress of the disease and the diagnostic process, including some of the most common diagnostic traps. The paper highlights a range of symptoms that should serve as a potential warning signal for clinicians-not just neurologists-indicating the need to evaluate the patient more thoroughly.

Indexed as

cortical ribbon signCreutzfeldt–Jakob diseaseprotein 14-3-3rapidly progressive dementiaRT-QuIC

Identifiers

PMID41874038
PMCPMC13010748

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Registered trials

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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.