Evidence map›Paper›PMID 36825462›Full record

ArticleBrain : a journal of neurology2023

Reply: De novo mutations in CLDN5: alternating hemiplegia of childhood or not?

Isabelle Desguerre, Melodie Aubart, Yosuke Hashimoto, Karine Poirier, Anna Kaminska, Marianne Alison, Nathalie Boddaert, Arnold Munnich, Matthew Campbell

Abstract readEditorialComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain : a journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Isabelle DesguerreDepartments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Melodie AubartDepartments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Yosuke HashimotoSmurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
Karine PoirierINSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.
Anna KaminskaDepartments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Marianne AlisonDepartment of Pediatric Radiology, Hospital Robert Debré, Université Paris Cité, Paris F-75015, France.
Nathalie BoddaertDepartments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Arnold MunnichDepartments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.
Matthew CampbellSmurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0003-3008-9563

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HemiplegiaClaudin-5HumansMutationClaudin-5CLDN5 protein, human

Identifiers

PMID36825462
PMCPMC10393392

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.