Evidence map›Paper›PMID 41013921›Full record

ArticleMovement disorders clinical practice2026

Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15".

Haya S AlFaris, Sangeetha Yoganathan, Marcus N Callister, Liali Aljouda, Vivek Pai, Pradeep Krishnan, Andrea LeBlanc Miller, Christos Ganos, Carolina Gorodetsky

Abstract readLetter
In one paragraph

Article in Movement disorders clinical practice, 2026. 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

9 authors.

Haya S AlFarisDivision of Neurology, The Hospital For Sick Children, Toronto, Ontario, Canada.
Sangeetha YoganathanDivision of Neurology, The Hospital For Sick Children, Toronto, Ontario, Canada.
Marcus N CallisterDivision of Neurology, Department of Medicine, University of Toronto, UHN and UHN Foundation, Toronto, Ontario, Canada.
Liali AljoudaClinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Vivek PaiDivision of Neuroradiology, Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Pradeep KrishnanDivision of Neuroradiology, Department of Diagnostic and Interventional Radiology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Andrea LeBlanc MillerDivision of Neurology, The Hospital For Sick Children, Toronto, Ontario, Canada.
Christos GanosDivision of Neurology, Department of Medicine, University of Toronto, UHN and UHN Foundation, Toronto, Ontario, Canada.
Carolina GorodetskyDivision of Neurology, The Hospital For Sick Children, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0003-0007-9591

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

COX15 deficiencydystoniaLeigh syndromemitochondrial disorders

Identifiers

PMID41013921
PMCPMC13042835

What Socratic 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 Socratic graph.