Evidence map›Paper›PMID 39206934›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2024

Potassium Channel Subunit Kir4.1 Mutated in Paroxysmal Kinesigenic Dyskinesia: Screening of an Italian Cohort.

Giovanna Zorzi, Federica Zibordi, Ugo Sorrentino, Holger Prokisch, Barbara Garavaglia, Michael Zech

Abstract readLetter
PubMed Full text at PMC Publisher
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Juvenile Dystonia Associated with Heterozygous Missense Variant in KCNJ10.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  2. Rare Movement Disorders-An Approach for Clinicians.International journal of molecular sciences · 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

6 authors.

Giovanna ZorziUnit of Child Neuropsychiatry-Movement Disorder, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID https://orcid.org/0000-0001-7041-5365
Federica ZibordiUnit of Child Neuropsychiatry-Movement Disorder, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Ugo SorrentinoInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.
Holger ProkischInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.
Barbara GaravagliaMedical Genetics and Neurogenetics Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Michael ZechInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.ORCID https://orcid.org/0000-0001-8112-9153

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39206934
PMCPMC11657011

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.