Evidence map›Paper›PMID 32146693›Full record

ArticleCerebellum (London, England)2020

Neurological Phenotypes Associated with AAAS-Related Disorders: Spastic Ataxia and Complex Spastic Paraplegia.

Cláudia Fernandes Lorea, Renata Barreto Tenório, Michel Koenig, Angela Huebner, Katrin Koehler, David Devos, Claire Guissart, Jonas Alex Morales Saute

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2020. 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

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.

Cláudia Fernandes LoreaHospital Escola da Universidade Federal de Pelotas, Pelotas, RS, Brazil.
Renata Barreto TenórioMedical Genetics Division, Hospital de Clínicas de Porto Alegre (HCPA), Rua Ramiro Barcelos 2350, Porto Alegre, RS, Zip Code 90.035-903, Brazil.
Michel KoenigLaboratoire de Génétique de Maladies Rares EA7402, Institut Universitaire de Recherche Clinique, Université de Montpellier, Montpellier, France.
Angela HuebnerKlinik und Poliklinik für Kinder- und Jugendmedizin, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Katrin KoehlerKlinik und Poliklinik für Kinder- und Jugendmedizin, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
David DevosPole de Neurologie Department of Neurology and Movement Disorders, Université Lille Nord De France, Université de Médecine, XEA 5947, IMPRT, CHU, 59037, Lille, France.
Claire GuissartLaboratoire de Génétique de Maladies Rares EA7402, Institut Universitaire de Recherche Clinique, Université de Montpellier, Montpellier, France.
Jonas Alex Morales SauteMedical Genetics Division, Hospital de Clínicas de Porto Alegre (HCPA), Rua Ramiro Barcelos 2350, Porto Alegre, RS, Zip Code 90.035-903, Brazil. jsaute@hcpa.edu.br.ORCID http://orcid.org/0000-0003-1141-6573

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultBrazilFemaleHumansIntellectual DisabilityMaleMoroccoMuscle SpasticityMutationNerve Tissue ProteinsNuclear Pore Complex ProteinsOptic AtrophyPedigreePhenotypeSpastic Paraplegia, HereditarySpinocerebellar AtaxiasAAAS protein, humanNerve Tissue ProteinsNuclear Pore Complex Proteins

Identifiers

PMID32146693

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.