Evidence map›Paper›PMID 36029213›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2022

Family History for Neurodegeneration in Multiple System Atrophy: Does it Indicate Susceptibility?

Fabian Leys, Sabine Eschlböck, Nicole Campese, Philipp Mahlknecht, Marina Peball, Georg Goebel, Victoria Sidoroff, Roberta Granata, Vincenzo Bonifati, Johannes Zschocke and 5 more

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Multiple system atrophy: cure and care.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  2. Article
  3. Parkinson's Disease is Predominantly a Genetic Disease.Journal of Parkinson's disease · 2024
    Review
  4. 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

15 authors.

Fabian LeysDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-1714-5305
Sabine EschlböckDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-3410-1243
Nicole CampeseDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-9980-3086
Philipp MahlknechtDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-0671-0516
Marina PeballDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-0791-7300
Georg GoebelDepartment of Medical Statistics, Informatics and Health Economics, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-7454-6212
Victoria SidoroffDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-7434-6229
Roberta GranataDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Vincenzo BonifatiDepartment of Clinical Genetics, University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-9334-1263
Johannes ZschockeInstitute of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-0046-8274
Stefan KiechlDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-9836-2514
Werner PoeweDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-4367-0971
Klaus SeppiDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-6503-1455
Gregor K WenningDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-9077-1666
Alessandra FanciulliDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-2854-4179

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Multiple System AtrophyParkinson Diseasealpha-SynucleinHumansalpha-Synucleinfamilialfamily historygeneticsmultiple system atrophyParkinson's disease

Identifiers

PMID36029213
PMCPMC9804463

What OpenQuestion holds

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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.