Evidence map›Paper›PMID 41301446›Full record

ReviewBiomolecules2025

Molecular Pathogenesis of Inherited Platelet Dysfunction.

Agustín Rodríguez-Alén, Antonio Moscardó, José M Bastida, José Rivera

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Biomolecules, 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

4 authors.

Agustín Rodríguez-AlénServicio de Hematología, Hospital Universitario de Toledo, 45007 Toledo, Spain.ORCID 0000-0003-3583-2977
Antonio MoscardóServicio de Hematología, Hospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, 46001 Valencia, Spain.ORCID 0000-0002-2865-1417
José M BastidaServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), 37008 Salamanca, Spain.ORCID 0000-0002-8007-3909
José RiveraServicio de Hematología, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, CIBERER-ISCIII, 30003 Murcia, Spain.ORCID 0000-0003-4225-6840

Funding

Fundación Séneca - Agencia de Ciencia y Tecnología de la Región de Murcia 21920/PI/22Gerencia Regional de Salud GRS2551/A/22-GRS2907/A1/2023-GRS2727/A1/23Instituto de Salud Carlos III (ISCIII) & European Union PI23/00624&PI24/01458ISCIII & CIBER CB15/00055ISCIII & European Union- NextGeneration EU and for PRTR PMP21/00052Sociedad Española de Trombosis y Hemostasia (SETH) Premio López Borrasca-Ayuda a Grupos de Trabajo-GEAPC
6 · The paper itself

Abstract

Inherited platelet function disorders (IPFD) are characterized by normal platelet count and morphology but impaired function due to pathogenic variants in genes encoding membrane receptors, granule constituents, or intracellular signaling proteins. Glanzmann's thrombasthenia, the most representative IPFD, results from

Indexed as

Blood Platelet DisordersBlood PlateletsHumansMutationSignal Transductioncongenital platelet signaling defectsGlanzmann thrombastheniaHermansky–Pudlak syndromeinherited platelet function disordersplatelet granule deficiency

Identifiers

PMID41301446
PMCPMC12649936

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.