Evidence map›Paper›PMID 27653636›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2016

Dystonia in ATP2B3-associated X-linked spinocerebellar ataxia.

Timothy Feyma, Keri Ramsey, C4RCD Research Group, Matthew J Huentelman, David W Craig, Sergio Padilla-Lopez, Vinodh Narayanan, Michael C Kruer

Abstract readCase ReportsLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. A Case Report of Cardiofaciocutaneous Syndrome withPharmacogenomics and personalized medicine · 2023
    Article
  4. Article
  5. Article
  6. 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

8 authors at 5 institutions in 1 country.

Timothy FeymaDivision of Pediatric Neurology, Gillette Children's Hospital, St. Paul, Minnesota, USA.
Keri RamseyCenter for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.
C4RCD Research Group
Matthew J HuentelmanCenter for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.
David W CraigCenter for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.
Sergio Padilla-LopezDepartment of Child Health, University of Arizona College of Medicine Phoenix, Phoenix, Arizona, USA.
Vinodh NarayananCenter for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.
Michael C KruerProgram in Neuroscience, Arizona State University, Tempe, Arizona, USA.
Translational Genomics Research Institute · USArizona State University · USGillette Children's Specialty Healthcare · USUniversity of Arizona · USUniversity of Phoenix · US

Funding

Molecular mechanisms of mitochondrial dysfunction in ATP13A2-associated neurodegeK08NS083739 · NINDS · UNIVERSITY OF ARIZONA · PI KRUER, MICHAEL C · 2013 to 2017
$869k
Doris Duke Charitable Foundation 2014112NINDS NIH HHS K08 NS083739
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultChildDystoniaFemaleGenetic Diseases, X-LinkedHumansMaleOlivopontocerebellar AtrophiesPedigreePlasma Membrane Calcium-Transporting ATPasesSpinocerebellar AtaxiasATP2B3 protein, humanPlasma Membrane Calcium-Transporting ATPases

Identifiers

PMID27653636
PMCPMC5380585
OpenAlexW2525682839

What OpenQuestion holds

Textmetadata
LicenceTDM
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.