Evidence map›Paper›PMID 35088096›Full record

ArticleNeuroradiology2022

Multimodal imaging of a patient with RAB39B mutation.

Laurane Mackels, Martin Moïse, Frédérique Depierreux

Open access · greenAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Neuroradiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Early Levodopa-Induced Motor Complications in RAB39B X-Linked Parkinsonism.Tremor and other hyperkinetic movements (New York, N.Y.) · 2024
    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

3 authors at 2 institutions in 1 country.

Laurane MackelsDepartment of Neurology, CHR Citadelle of Liège, Liège, Belgium.ORCID http://orcid.org/0000-0002-2132-3736
Martin MoïseDepartment of Radiology, University Hospital (CHU) of Liège, Liège, Belgium.ORCID http://orcid.org/0000-0003-3874-2213
Frédérique DepierreuxDepartment of Neurology, University Hospital (CHU) of Liège, Liège, Belgium.ORCID http://orcid.org/0000-0001-7949-8611
Centre hospitalier régional de la Citadelle · BEUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in RAB39B gene have been linked to intellectual deficiency associated with parkinsonism, also referred as to Waisman syndrome. As it appears to be a very rare cause of Parkinson Disease (PD), with only few cases described in the literature, the typical clinical and radiological features are yet to be determined. In this article, we report and illustrate multimodal brain imaging by computed tomography, magnetic resonance imaging, transcranial ultrasound (US), dopamine transporter single photon emission computed tomography and [

Indexed as

Fluorodeoxyglucose F18Parkinson DiseaseAdultHumansMaleMultimodal ImagingMutationPositron-Emission Tomographyrab GTP-Binding ProteinsFluorodeoxyglucose F18Rab39B protein, humanrab GTP-Binding ProteinsMultimodal imagingParkinsonismRAB39BWaisman syndrome

Identifiers

PMID35088096
OpenAlexW4210429982

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.