Evidence map›Paper›PMID 32830305›Full record

ArticleNeurogenetics2021

Familial writer's cramp: a clinical clue for inherited coenzyme Q

Matthias Amprosi, Michael Zech, Ruth Steiger, Wolfgang Nachbauer, Andreas Eigentler, Elke R Gizewski, Michael Guger, Elisabetta Indelicato, Sylvia Boesch

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Neurogenetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Tremors with dystonia as a predominant manifestation of primary coenzyme Q10 deficiency.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  2. Article
  3. Understanding coenzyme Q.Physiological reviews · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Metabolites · 2022
    Review
  8. Autosomal recessive adult onset ataxia.Journal of neurology · 2022
    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

9 authors at 3 institutions in 2 countries.

Matthias AmprosiCenter for Rare Neurological Diseases, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Michael ZechInstitut für Neurogenomik, Helmholtz Zentrum München, Oberschleißheim, Munich, Germany.
Ruth SteigerNeuroimaging Research Core Facility, Medical University of Innsbruck, Innsbruck, Austria.
Wolfgang NachbauerCenter for Rare Neurological Diseases, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Andreas EigentlerCenter for Rare Neurological Diseases, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Elke R GizewskiNeuroimaging Research Core Facility, Medical University of Innsbruck, Innsbruck, Austria.
Michael GugerClinic for Neurology 2, Kepler University Hospital GmbH, Linz, Austria.
Elisabetta IndelicatoCenter for Rare Neurological Diseases, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria. elisabetta.indelicato@i-med.ac.at.ORCID 0000-0003-0217-8630
Sylvia BoeschCenter for Rare Neurological Diseases, Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Innsbruck Medical University · ATHelmholtz Zentrum München · DEKepler Universitätsklinikum · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spectrum of coenzyme Q

Indexed as

AdultAtaxiaCerebellar AtaxiaDystonic DisordersFemaleHomozygoteHumansMitochondrial ProteinsMutationUbiquinonecoenzyme Q10Mitochondrial ProteinsUbiquinoneUbiquinone Q2AtaxiaCoenzyme Q10DystoniaMagnetic resonance spectroscopyMitochondrial diseaseUbiquinone

Identifiers

PMID32830305
PMCPMC7997836
OpenAlexW3081378844

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.