Evidence map›Paper›PMID 38775934›Full record

ArticleJournal of neurology2024

Dystonia and mitochondrial disease: the movement disorder connection revisited in 900 genetically diagnosed patients.

Elisabetta Indelicato, Lea D Schlieben, Sarah L Stenton, Sylvia Boesch, Matej Skorvanek, Jan Necpal, Robert Jech, Juliane Winkelmann, Holger Prokisch, Michael Zech

Abstract readLetter
In one paragraph

Article in Journal of neurology, 2024. 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
–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

6 citing papers in PubMed.

  1. Dystonia: Insights into Mechanisms and Novel Therapeutics.Current neurology and neuroscience reports · 2026
    Review
  2. Article
  3. 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

10 authors.

Elisabetta Indelicato *Institute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany.
Lea D Schlieben *Institute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany.
Sarah L StentonDivision of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Sylvia BoeschCenter for Rare Movement Disorders Innsbruck, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Matej SkorvanekDepartment of Neurology, P. J. Safarik University, Kosice, Slovakia.
Jan Necpal2nd Department of Neurology, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Robert JechDepartment of Neurology, Charles University in Prague, 1st Faculty of Medicine and General University Hospital in Prague, Kateřinská 30, 121 08, Prague, Czech Republic.
Juliane WinkelmannInstitute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany.
Holger Prokisch *Institute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany.
Michael Zech *Institute of Human Genetics, Technical University of Munich, School of Medicine, Munich, Germany. michael.zech@mri.tum.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DystoniaMitochondrial DiseasesAdolescentAdultFemaleHumansMaleMiddle AgedMovement DisordersMutation

Identifiers

PMID38775934
PMCPMC11233361

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.