Evidence map›Paper›PMID 41935079›Full record

ReviewNPJ Parkinson's disease2026

Progress in modelling ATP13A2-linked neurodegeneration.

Benedetta Balbo, Rémi Kinet, Laura Civiero, Benjamin Dehay

Abstract readReview
In one paragraph

Review in NPJ Parkinson's disease, 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.

Benedetta Balbo *Department of Biology, University of Padova, Padova, Italy.
Rémi Kinet *Univ. Bordeaux, CNRS, IMN, UMR 5293, F-33000, Bordeaux, France.
Laura CivieroDepartment of Biology, University of Padova, Padova, Italy.
Benjamin DehayUniv. Bordeaux, CNRS, IMN, UMR 5293, F-33000, Bordeaux, France. benjamin.dehay@u-bordeaux.fr.

Funding

Agence Nationale de la Recherche ANR-21-CE18-0025-01 NOVELFondation Maladies Rares Project Grant No. 10877 (2016)Fondation pour la Recherche Médicale Prix MARIE_PAULE BURRUS 2024 - PRS202407019918
6 · The paper itself

Abstract

ATP13A2 is a lysosomal P5-ATPase highly expressed in the central nervous system, regulating polyamine, metal cation, and calcium homeostasis. Loss-of-function mutations cause an autosomal recessive juvenile form of Parkinson's disease called Kufor-Rakeb syndrome and other neurodegenerative disorders. Since the first clinical discovery of the Kufor-Rakeb syndrome, numerous ATP13A2-related models have emerged, leading to significant advances in understanding the physiology and pathophysiology of this protein. This review summarizes ATP13A2 structure, function, pathology, and insights gained from cellular and animal models, highlighting their value for elucidating disease mechanisms and therapeutic development across species and experimental systems, relevant to neurodegeneration research broadly.

Identifiers

PMID41935079
PMCPMC13230722

What Socratic 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 Socratic graph.