Evidence map›Paper›PMID 37303095›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2023

Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST.

Joana Damásio, Clara Barbot, Rui Felgueiras, Ana Filipa Brandão, José Barros, Jorge Oliveira, Jorge Sequeiros

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2023. 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
–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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Joana DamásioNeurology Department, Centro Hospitalar Universitário do Porto, Porto, Portugal.ORCID 0000-0002-6539-6398
Clara BarbotUnidade de Investigação Genética e Epidemiológica em Doenças Neurológicas, Institute for Molecular and Cell Biology, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-5597-107X
Rui FelgueirasNeurology Department, Centro Hospitalar Universitário do Porto, Porto, Portugal.ORCID 0000-0001-9372-8743
Ana Filipa BrandãoCentre for Predictive and Preventive Genetics, Institute for Molecular and Cell Biology, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-0409-959X
José BarrosNeurology Department, Centro Hospitalar Universitário do Porto, Porto, Portugal.ORCID 0000-0001-6183-5050
Jorge OliveiraUnidade de Investigação Genética e Epidemiológica em Doenças Neurológicas, Institute for Molecular and Cell Biology, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0003-3924-6385
Jorge SequeirosUnidade de Investigação Genética e Epidemiológica em Doenças Neurológicas, Institute for Molecular and Cell Biology, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.ORCID 0000-0002-9846-1037

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Spastic Paraplegia, HereditaryHumansSpastinSpastinSPAST protein, human

Identifiers

PMID37303095

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.