Evidence map›Paper›PMID 36362324›Full record

ArticleInternational journal of molecular sciences2022

Neurodegenerative Disorder Risk in Krabbe Disease Carriers.

Lorenza Vantaggiato, Enxhi Shaba, Alfonso Carleo, Daiana Bezzini, Giovanna Pannuzzo, Alice Luddi, Paola Piomboni, Luca Bini, Laura Bianchi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

Lorenza VantaggiatoFunctional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.ORCID 0000-0003-4078-7250
Enxhi ShabaFunctional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.ORCID 0000-0002-9561-2426
Alfonso CarleoDepartment of Pulmonology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.
Daiana BezziniDepartment of Life Sciences, University of Siena, 53100 Siena, Italy.
Giovanna PannuzzoDepartment of Biochemical and Biotechnological Sciences, Section of Physiology, University of Catania, 95121 Catania, Italy.
Alice LuddiDepartment of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy.ORCID 0000-0002-4946-7336
Paola PiomboniDepartment of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy.
Luca BiniFunctional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.ORCID 0000-0001-8951-2106
Laura BianchiFunctional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.
University of Siena · ITMedizinische Hochschule Hannover · DEUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Krabbe disease (KD) is a rare autosomal recessive disorder caused by mutations in the galactocerebrosidase gene (

Indexed as

Leukodystrophy, Globoid CellNeurodegenerative DiseasesAnimalsDisease Models, AnimalGalactosylceramidaseMiceProteomicsGalactosylceramidaseAlzheimer diseasedemyelinationgloboid cell leukodystrophyLewy bodymultiple sclerosisneurodegenerationneuroinflammationParkinson diseaseubiquitin dependent degradation

Identifiers

PMID36362324
PMCPMC9654610
OpenAlexW4308876456

What OpenQuestion 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 OpenQuestion graph.