Evidence map›Paper›PMID 41048925›Full record

ArticleNeurology. Genetics2025

Alternating Hemiplegia of Childhood and

Alexander J Simpson, Ailsa McLellan, Katherine Elizabeth Behl, Jo Brown, Steven J Clapcote, J Helen Cross, Arn M J M van den Maagdenberg, Aikaterini None Vezyroglou, Simona Balestrini, Sanjay M Sisodiya

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Neurology. Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Clinical and Genetic Spectrum ofNeurology. Genetics · 2026
    Article
  2. Mechanism of Rescue of NaInternational journal of molecular sciences · 2026
    Article
  3. ATP1A3: Uncommon and wavering epilepsy phenotype in a rare variant.Epileptic disorders : international epilepsy journal with videotape · 2026
    Article
  4. 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

10 authors.

Alexander J SimpsonNeurosciences Department, Royal Hospital for Children and Young People, Edinburgh, UK.ORCID https://orcid.org/0009-0003-8092-5221
Ailsa McLellanNeurosciences Department, Royal Hospital for Children and Young People, Edinburgh, UK.ORCID https://orcid.org/0009-0003-7301-7305
Katherine Elizabeth BehlAHC UK Charity, London, UK.ORCID https://orcid.org/0009-0005-9020-0384
Jo BrownAHC UK Charity, London, UK.ORCID https://orcid.org/0009-0005-7749-3901
Steven J ClapcoteSchool of Biomedical Sciences, University of Leeds, UK.ORCID https://orcid.org/0000-0002-6662-5690
J Helen CrossUCL NIHR Great Ormond Street Institute of Child Health, London, UK.ORCID https://orcid.org/0000-0001-7345-4829
Arn M J M van den MaagdenbergDepartment of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
Aikaterini None VezyroglouGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.ORCID https://orcid.org/0000-0001-6495-0863
Simona BalestriniNeuroscience and Medical Genetics Department, Meyer Children's Hospital, IRCSS - University of Florence, Italy.ORCID https://orcid.org/0000-0001-5639-1969
Sanjay M SisodiyaDepartment of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.ORCID https://orcid.org/0000-0002-1511-5893

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This report presents key insights from the 2022 annual conference held in Edinburgh, commemorating the 10th anniversary of the discovery of

Identifiers

PMID41048925
PMCPMC12488843

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.