Evidence map›Paper›PMID 42883914›Full record

ArticleInternational journal of molecular sciences2026

Molecular and Structural Characterization of Five Novel

Monia Anania, Veronica Pagliardini, Marco Spada, Laura Econimo, Irene Giacalone, Martina Vinci, Paolo Colomba, Francesca Cappelletti, Carmelo Tonelli, Michelangelo Mancuso and 4 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 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

14 authors.

Monia AnaniaInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.
Veronica PagliardiniDepartment of Pediatrics, University of Torino, 10126 Torino, Italy.
Marco SpadaDepartment of Pediatrics, University of Torino, 10126 Torino, Italy.ORCID 0000-0002-8894-350X
Laura EconimoNephrology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia-ASST Spedali Civili of Brescia, 25100 Brescia, Italy.
Irene GiacaloneInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.
Martina VinciInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.
Paolo ColombaInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.ORCID 0000-0002-2470-7030
Francesca CappellettiNephrology Unit, Policlinico Le Scotte, 53100 Siena, Italy.
Carmelo TonelliCardiology Unit, Vittorio Emanuele Hospital, 93012 Gela, Italy.
Michelangelo MancusoDepartment of Clinical and Experimental Medicine, Neurological Institute, University of Pisa, 56126 Pisa, Italy; michelangelo.mancuso@unipi.it .ORCID 0000-0003-2738-8562
Giulia DuroDepartment of Medical, Surgery and Health Sciences, University of Trieste, 34149 Trieste, Italy; giulia.duro@asugi.sanita.fvg.it .
Emanuela Maria MarsanaInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.
Marta MoschettiInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.ORCID 0009-0008-2119-7988
Giovanni DuroInstitute for Biomedical Research and Innovation (IRIB), National Research Council (CNR), 90146 Palermo, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease is an X-linked lysosomal storage disorder caused by pathogenic variants in the

Indexed as

alpha-GalactosidaseFabry DiseaseCatalytic DomainGlycosylationHumansModels, MolecularMutationProtein ConformationProtein FoldingTrihexosylceramidesalpha-GalactosidaseGLA protein, humanglobotriaosylceramideTrihexosylceramidesFabry diseaseGLA geneLyso-Gb3novel mutationsα-galactosidase A

Identifiers

PMID42883914
PMCPMC13664900

What OpenQuestion holds

Textmetadata
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.