Evidence map›Paper›PMID 38247386›Full record

ArticleMovement disorders clinical practice2024

"Alternating" the Diagnosis after 40 Years of Disease: The Thousand Faces of ATP1A3 Mutation.

Silvia Gallo, Fabienne Ory-Magne, Clémence Leung, Margherita Fabbri, Bastien Estublier, Emmanuel Cheuret, Olivier Patat, Raquel Pinheiro Barbosa

Abstract readCase ReportsLetter
In one paragraph

Article in Movement disorders clinical practice, 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. Clinical and Genetic Spectrum ofNeurology. Genetics · 2026
    Article
  2. 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

8 authors.

Silvia GalloDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-7223-2060
Fabienne Ory-MagneDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-6179-4500
Clémence LeungDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.
Margherita FabbriDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-7250-592X
Bastien EstublierNeuropediatric Department, Toulouse-Purpan University Hospital, Toulouse, France.
Emmanuel CheuretNeuropediatric Department, Toulouse-Purpan University Hospital, Toulouse, France.
Olivier PatatDepartment of Medical Genetics, Toulouse University Hospital, Toulouse, France.
Raquel Pinheiro BarbosaDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationSodium-Potassium-Exchanging ATPaseFemaleHumansMaleATP1A3 protein, humanSodium-Potassium-Exchanging ATPase

Identifiers

PMID38247386
PMCPMC11322589

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.