Evidence map›Paper›PMID 40868272›Full record

ArticleBiomedicines2025

Vestibular Deficit in Patients with Waardenburg Syndrome.

Mathilde Benifla, Margaux Serey-Gaut, Emilie Bois, Salma Jbyeh, Natacha Teissier, Monique Elmaleh-Bergès, Laurence Jonard, Véronique Pingault, Natalie Loundon, Kahina Belhous and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Biomedicines, 2025. 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

12 authors.

Mathilde BeniflaDepartment of Otolaryngology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.ORCID 0000-0001-9144-2143
Margaux Serey-GautDepartment of Genetics, Necker Hospital, CRMR Surdités Génétiques, Service Médecine Génomique des Maladies Rares, UF Développement et Morphogenèse, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.ORCID 0000-0002-1165-0872
Emilie BoisDepartment of Otolaryngology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.
Salma JbyehDepartment of Otolaryngology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.
Natacha TeissierDepartment of Otolaryngology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.
Monique Elmaleh-BergèsDepartment of Pediatric Radiology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.
Laurence JonardDepartment of Genetics, Necker Hospital, CRMR Surdités Génétiques, Service Médecine Génomique des Maladies Rares, UF Développement et Morphogenèse, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.
Véronique PingaultDepartment of Genetics, Necker Hospital, CRMR Surdités Génétiques, Service Médecine Génomique des Maladies Rares, UF Développement et Morphogenèse, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.
Natalie LoundonCentre de Recherche en Audiologie, Necker Hospital, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.
Kahina BelhousDepartment of Pediatric Radiology, Necker Hospital, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.
Sandrine MarlinDepartment of Genetics, Necker Hospital, CRMR Surdités Génétiques, Service Médecine Génomique des Maladies Rares, UF Développement et Morphogenèse, AP-HP, Faculty of Medicine, Paris University, F-75015 Paris, France.ORCID 0000-0002-4115-9806
Audrey MaudouxDepartment of Otolaryngology, Robert Debré Hospital, AP-HP, Faculty of Medicine, Paris University, F-75019 Paris, France.

Funding

Assistance Publique - Hôpitaux de Paris Poste d'accueil scholarship
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

balancehearing lossinner ear malformationsvestibular functionWaardenburg syndrome

Identifiers

PMID40868272
PMCPMC12383285

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.