Evidence map›Paper›PMID 39140302›Full record

ArticleMovement disorders clinical practice2024

"Relapsing-Remitting" Ataxia and Unexpected Brain Imaging in a Child with HIBCH Deficiency.

Simone Gana, Gloria Rossetto, Jessica Garau, Valeria Vacchini, Francesca Ferraro, Elisa Rognone, Anna Pichiecchio, Serena Gasperini, Enza Maria Valente, Simona Orcesi

Abstract readLetter
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. 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

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.

Simone GanaNeurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.
Gloria RossettoDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Jessica GarauNeurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.
Valeria VacchiniDepartment of Child Neurology and Psychiatry, IRCSS Mondino Foundation, Pavia, Italy.
Francesca FerraroDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Elisa RognoneDepartment of Neuroradiology, IRCSS Mondino Foundation, Pavia, Italy.
Anna PichiecchioDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
Serena GasperiniDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Enza Maria ValenteNeurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.ORCID https://orcid.org/0000-0002-0600-6820
Simona OrcesiDepartment of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.

Funding

Italian Ministry of Health RCR-2022-23682289Italian Ministry of Health Ricerca Corrente 2022-2024
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ataxiabrain MRIHIBCH deficiencyLeigh‐like syndromewhole exome sequencing

Identifiers

PMID39140302
PMCPMC11542274

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.