Evidence map›Paper›PMID 38556906›Full record

ArticleMovement disorders clinical practice2024

Primary Coenzyme Q10 Deficiency-4 Causing Young Onset Ataxia-Dystonia.

Divya M Radhakrishnan, Arti Saini, Saman Fatima, Anu Gupta, Venugopalan Y Vishnu, Mamta Bhushan Singh, Rohit Bhatia, M V Padma Srivastva, Achal K Srivastava, Roopa Rajan

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. 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. Article
  2. Tremors with dystonia as a predominant manifestation of primary coenzyme Q10 deficiency.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    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.

Divya M RadhakrishnanDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-0641-7398
Arti SainiDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0001-5223-9206
Saman FatimaDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Anu GuptaDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-0095-6569
Venugopalan Y VishnuDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-3654-8137
Mamta Bhushan SinghDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Rohit BhatiaDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.
M V Padma SrivastvaDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.
Achal K SrivastavaDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0002-4590-7947
Roopa RajanDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India.ORCID 0000-0003-4987-7252

Funding

Department of Biotechnology, India BT/PR26428/MED/12/783/2017
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cerebellar AtaxiaDystoniaMitochondrial DiseasesMuscle WeaknessAtaxiaHumansUbiquinoneUbiquinone

Identifiers

PMID38556906
PMCPMC10982600

What OpenQuestion holds

Textmetadata
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.