Evidence map›Paper›PMID 41077880›Full record

ArticleNeuropathology : official journal of the Japanese Society of Neuropathology2025

Atypical Frontotemporal Dementia Associated With SQSTM1 Gene Mutation: A Clinicopathological Case.

Christian Espinoza-Vinces, María Victoria Zelaya Huerta, Valle Coca Pueyo, Genoveva Montoya-Murillo, Ana Patiño-García, Rafael Villino-Rodríguez, Ainhoa Atorrasagasti-Villar, Javier Arbizu, Mario Riverol

Abstract readCase Reports
In one paragraph

Article in Neuropathology : official journal of the Japanese Society of Neuropathology, 2025. 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. Atypical Frontotemporal Dementia Associated With SQSTM1 Gene Mutation: A Clinicopathological Case.Neuropathology : official journal of the Japanese Society of Neuropathology · 2025
    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

9 authors.

Christian Espinoza-VincesDepartment of Neurology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID https://orcid.org/0009-0003-1905-421X
María Victoria Zelaya HuertaDepartment of Pathology, University Hospital of Navarra, Pamplona, Spain.
Valle Coca PueyoBrain Bank of Navarra, Navarrabiomed, Fundación Miguel Servet, Pamplona, Spain.
Genoveva Montoya-MurilloDepartment of Neurology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID https://orcid.org/0000-0003-3994-8993
Ana Patiño-GarcíaNavarra Institute for Heath Research (IdiSNA), Pamplona, Spain.ORCID https://orcid.org/0000-0002-4066-8203
Rafael Villino-RodríguezDepartment of Neurology, Clínica Universidad de Navarra, Pamplona, Spain.
Ainhoa Atorrasagasti-VillarDepartment of Neurology, Clínica Universidad de Navarra, Pamplona, Spain.
Javier ArbizuNavarra Institute for Heath Research (IdiSNA), Pamplona, Spain.ORCID https://orcid.org/0000-0002-8370-5510
Mario RiverolDepartment of Neurology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID https://orcid.org/0000-0002-4383-9127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 78-year-old man presented with a six-year history of progressive memory decline, initially manifesting as recent memory impairment and mild anomia, which gradually evolved into motor clumsiness, gait disturbances, language difficulties, behavioral changes, and late-onset parkinsonism. He had been diagnosed with Paget disease of bone (PDB) at the age of 45. Brain MRI revealed asymmetric left anterior temporal atrophy, while [

Indexed as

Frontotemporal DementiaSequestosome-1 ProteinAgedBrainHumansMaleMutationSequestosome-1 ProteinSQSTM1 protein, humandementiaFTLDSQSTM1TDP‐43

Identifiers

PMID41077880
PMCPMC12516176

What OpenQuestion holds

Textmetadata
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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.