Evidence map›Paper›PMID 39404500›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2024

Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case Report.

Barbara Castellotti, Cinzia Gellera, Davide Caputo, Federica Rachele Danti, Giuliana Messina, Marinella Corbetta, Stefania Magri, Franco Taroni, Holger Prokisch, Michael Zech and 1 more

Abstract readLetter
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.Movement disorders : official journal of the Movement Disorder Society · 2025
    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

11 authors.

Barbara CastellottiUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Cinzia GelleraUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Davide CaputoUnit of Developmental Neurology-Epileptology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Federica Rachele DantiUnit of Child Neuropsychiatry-Movement Disorder, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Giuliana MessinaUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Marinella CorbettaUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Stefania MagriUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Franco TaroniUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Holger ProkischInstitute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.
Michael ZechInstitute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.
Giovanna ZorziUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID https://orcid.org/0000-0001-7041-5365

Funding

Bundesministerium für Bildung und Forschung 01GM2302Deutsche Forschungsgemeinschaft DFG 458949627Deutsche Forschungsgemeinschaft ZE 1213/2-1Else Kröner-Fresenius-Stiftung 2022_EKSE.185European Joint Program on Rare Disease JTC 2022Freistaat BayernMinistero della Salute RCC RF-212370491Technische Universität München
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DNA polymerase gamma (POLG)next generation sequencing (NGS)paroxysmal non‐kinesigenic dystinesias (PNKD)

Identifiers

PMID39404500
PMCPMC11657016

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.