Evidence map›Paper›PMID 35949253›Full record

ArticleNeurology. Genetics2022

A Second Case With the V374A

Flavia Palombo, Chiara La Morgia, Claudio Fiorini, Leonardo Caporali, Maria Lucia Valentino, Vincenzo Donadio, Rocco Liguori, Valerio Carelli

Open access · goldAbstract read
In one paragraph

Article in Neurology. Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 62% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Tremor in Spinocerebellar Ataxia: A Scoping Review.Tremor and other hyperkinetic movements (New York, N.Y.) · 2024
    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 at 1 institution in 1 country.

Flavia PalomboIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.ORCID https://orcid.org/0000-0002-1639-3764
Chiara La MorgiaIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.ORCID https://orcid.org/0000-0002-4639-8929
Claudio FioriniIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.
Leonardo CaporaliIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.ORCID https://orcid.org/0000-0002-0666-4380
Maria Lucia ValentinoIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.
Vincenzo DonadioIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.
Rocco LiguoriIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.
Valerio CarelliIRCCS Istituto delle Scienze Neurologiche di Bologna (F.P., C.L.M., C.F., L.C., M.L.V., V.C.), Programma di Neurogenetica, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna (C.L.M., V.D., R.L.), UOC Clinica Neurologica, Italy; and Department of Biomedical and NeuroMotor Sciences (DIBINEM) (M.L.V., R.L., V.C.), University of Bologna, Italy.
Istituto delle Scienze Neurologiche di Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: To date, approximately 20 heterozygous mainly loss-of-function variants in Methods: We describe the clinical history of a patient with SCA and conducted genetic investigations including mitochondrial DNA analysis and exome sequencing. Results: This male patient was reported to have unstable gait with tremors at the lower limbs and dysarthric speech since childhood. A neurologic examination also showed dysarthria, nystagmus, action tremor, dysmetria, and weak deep tendon reflexes. He had marked cerebellar atrophy at brain MRI, more evident at vermis. Molecular analysis, including exome sequencing and an in silico panel analysis of genes associated with SCA, revealed the c.1121T>C [p.V374A] mutation in Discussion: This report consolidates the pathogenicity of the V374A

Identifiers

PMID35949253
PMCPMC9359624
OpenAlexW4291020608

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.