Evidence map›Paper›PMID 39224875›Full record

ArticleClinical parkinsonism & related disorders2024

Dystonia: A novel sign of the Smith-Magenis syndrome - A three-case report.

Lukáš Kunc, Petra Havránková, Matěj Škorvánek, Iva Příhodová, Kamila Poláková, Lenka Nosková, Markéta Tesařová, Tomáš Honzík, Michael Zech, Robert Jech

Abstract readCase Reports
In one paragraph

Article in Clinical parkinsonism & related disorders, 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. Article
  2. 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.

Lukáš KuncDepartment of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Petra HavránkováDepartment of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Matěj ŠkorvánekDepartment of Neurology and Center for Rare Movement Disorders, Faculty of Medicine, P. J. Safarik University and University Hospital L. Pasteur, Kosice, Slovak Republic.
Iva PříhodováDepartment of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Kamila PolákováDepartment of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Lenka NoskováDepartment of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Markéta TesařováDepartment of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Tomáš HonzíkDepartment of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.
Michael ZechInstitute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.
Robert JechDepartment of Neurology, 1st Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Case reportDystoniaGenetic disorderSmith-Magenis syndrome

Identifiers

PMID39224875
PMCPMC11367135

What OpenQuestion holds

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Registered trials

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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.