Evidence map›Paper›PMID 33842081›Full record

ReviewNeurology. Clinical practice2021

Selective Bilateral Vestibular Neuropathy in a Turkish CMT1B Family With a Novel

Gülden Akdal, Koray Koçoğlu, Elçin Bora, Altuğ Koç, Ayfer Ülgenalp, Mithat Bedir, Rahmi Tümay Ala, Esra Battaloğlu, Günay Kırkım, İhsan Şükrü Şengün and 1 more

Open access · hybridAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Neurology. Clinical practice, 2021. 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
0.1field-weighted citation impact, top 59% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Neurological update: neuro-otology 2023.Journal of neurology · 2023
    Article
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

11 authors at 1 institution in 2 countries.

Gülden AkdalDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Koray KoçoğluDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Elçin BoraDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Altuğ KoçDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Ayfer ÜlgenalpDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Mithat BedirDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Rahmi Tümay AlaDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Esra BattaloğluDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Günay KırkımDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
İhsan Şükrü ŞengünDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Gábor Michael HalmágyiDepartment of Neurology (GA, RTA, İŞŞ) and Department of Neurosciences (GA, KK), Institute of Health Sciences, Department of Medical Genetics (E. Bora, AK, AÜ), Dokuz Eylül University, İzmir, Turkey; Department of Neurology (MB), Mardin State Hospital, Mardin, Turkey; Department of Molecular Biology and Genetics (E. Battaloğlu), Boğaziçi University, İstanbul, Turkey; Hearing, Speech and Balance Unit (GK), Department of Otorhinolaryngology, Dokuz Eylül University, İzmir, Turkey; and Department of Neurology (GMH), Royal Prince Alfred Hospital, University of Sydney, Australia.
Dokuz Eylül University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewTo report the findings in 12 members over 3 generations of a family with dominantly inherited Charcot-Marie-Tooth disease (CMT1B) due to a novel RECENT

findingsAll affected patients had a demyelinating neuropathy and a novel SUMMARY: Some CMT mutations can impair vestibular function, presumably because of a vestibular nerve involvement but spare hearing. In such patients, impairment of vestibular function and impairment of proprioception contribute to imbalance.

Identifiers

PMID33842081
PMCPMC8032420
OpenAlexW3085101317

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.