Evidence map›Paper›PMID 41002431›Full record

ReviewCells2025

Wings of Discovery: Using

Rachele Vivarelli, Chiara Vantaggiato, Maria Teresa Bassi, Filippo Maria Santorelli, Maria Marchese

Abstract readReview
In one paragraph

Review in Cells, 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. Review
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

5 authors.

Rachele VivarelliDepartment of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Calambrone, 56128 Pisa, Italy.ORCID 0009-0008-0450-2514
Chiara VantaggiatoLaboratory of Medical Genetics, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, 23842 Lecco, Italy.ORCID 0000-0002-3910-6836
Maria Teresa BassiLaboratory of Medical Genetics, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, 23842 Lecco, Italy.ORCID 0000-0002-8236-1197
Filippo Maria SantorelliDepartment of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Calambrone, 56128 Pisa, Italy.ORCID 0000-0002-1359-9062
Maria MarcheseDepartment of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Calambrone, 56128 Pisa, Italy.ORCID 0000-0002-0194-0702

Funding

Italian Minister of Health Ricerca Corrente 2024-2025Telethon Foundation GJC21131
6 · The paper itself

Abstract

Hereditary spastic paraplegia (HSP) and hereditary ataxias (HA) are clinically and genetically heterogeneous neurodegenerative disorders that primarily affect motor coordination and neural integrity. Despite distinct pathological features, such as pyramidal tract degeneration in HSP and spinocerebellar pathway involvement in HA, these conditions share overlapping genetic pathways and mechanisms. The fruit fly

Indexed as

Drosophila melanogasterSpastic Paraplegia, HereditaryAnimalsCRISPR-Cas SystemsDisease Models, AnimalHumansDisease modelingDrosophila melanogasterhereditary ataxiashereditary spastic paraplegia

Identifiers

PMID41002431
PMCPMC12469124

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.