Evidence map›Paper›PMID 39346806›Full record

ArticleTremor and other hyperkinetic movements (New York, N.Y.)2024

Tremor-Dominant Movement Disorder in

Antonia M Stehr, Thomas Koeglsperger, Maureen Jacob, Valerio Rhodio, Juliane Winkelmann, Franziska Hopfner, Michael Zech

Abstract readCase Reports
In one paragraph

Article in Tremor and other hyperkinetic movements (New York, N.Y.), 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. NovelSultan Qaboos University medical journal · 2026
    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

7 authors.

Antonia M Stehr *Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.ORCID 0000-0001-9932-5187
Thomas Koeglsperger *Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0001-6101-0323
Maureen JacobInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.
Valerio RhodioInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.
Juliane WinkelmannInstitute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.ORCID 0000-0002-3074-599X
Franziska Hopfner *Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0001-6524-0281
Michael Zech *Institute of Human Genetics, Technical University of Munich, School of Medicine and Health, Munich, Germany.ORCID 0000-0001-8112-9153

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: KBG syndrome is a monogenic disorder caused by heterozygous pathogenic variants in Case report: We report a 24-year-old patient harboring a pathogenic Discussion: Adding to the recently described individual, our present patient highlights the relevance of movement disorders as a clinically relevant manifestation of KBG syndrome.

Indexed as

Repressor ProteinsTremorAbnormalities, MultipleBone Diseases, DevelopmentalFaciesFemaleFrameshift MutationHumansIntellectual DisabilityMaleMicrocephalyTooth AbnormalitiesYoung AdultANKRD11 protein, humanRepressor ProteinsANKRD11combined tremor syndromeKBG syndrometremor

Identifiers

PMID39346806
PMCPMC11428658

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.