ArticleFrontiers in neurology2020
Is Ataxia an Underestimated Symptom of Huntington's Disease?
Open access · goldAbstract read
In one paragraph
Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
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.
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.
Who cites it
13 citing papers in PubMed, 18 citations in OpenAlex.
- Clinical and genetic diagnostic challenges in presumed hereditary ataxia.Journal of neurology · 2026Article
- Along-Tract Diffusion Alterations in the Dentato-Rubro-Thalamic Tract Correlate With Motor and Cognitive Decline in Huntington's Disease.Human brain mapping · 2025Article
- Deep Brain Stimulation Withdrawal without Relapse in Chorea-Acanthocytosis: Two Case Reports.Movement disorders clinical practice · 2025Article
- Ablation of TrkB from Enkephalinergic Precursor-Derived Cerebellar Granule Cells Generates Ataxia.Biology · 2024Article
- Reviewing the Structure-Function Paradigm in Polyglutamine Disorders: A Synergistic Perspective on Theoretical and Experimental Approaches.International journal of molecular sciences · 2024Review
- Cell-type-specific CAG repeat expansions and toxicity of mutant Huntingtin in human striatum and cerebellum.Nature genetics · 2024Article
- Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia.Journal of neurology · 2024Article
- "I don't have Huntington's disease": the boundaries between acceptance and understanding.Arquivos de neuro-psiquiatria · 2023Article
- Pathogenesis of Huntington's Disease: An Emphasis on Molecular Pathways and Prevention by Natural Remedies.Brain sciences · 2022Review
- Case report: Cerebellar sparing in juvenile Huntington's disease.Frontiers in neurology · 2022Article
- Juvenile-Onset Huntington Disease Pathophysiology and Neurodevelopment: A Review.Movement disorders : official journal of the Movement Disorder Society · 2022Review
- Huntington's disease: lessons from prion disorders.Journal of neurology · 2021Article
- It Is Time to Define Huntington's Disease Onset more Clearly.Movement disorders clinical practice · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
23 authors at 5 institutions in 1 country.
Gustavo L FranklinMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Carlos Henrique F CamargoMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Alex T MeiraMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Giovana M PavanelliMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Sibele S MilanoMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Francisco B GerminianiMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Nayra S C LimaFaculdade de Medicina, Universidade de Vila Velha, Espirito Santo, Brazil.
Salmo RaskinGenetika - Centro de Aconselhamento e Laboratório de Genética, Curitiba, Brazil.
Orlando Graziani Povoas BarsottiniDivision of General Neurology and Ataxia Unit, Department of Neurology, Federal University of São Paulo - UNIFESP, São Paulo, Brazil.
José Luiz PedrosoDivision of General Neurology and Ataxia Unit, Department of Neurology, Federal University of São Paulo - UNIFESP, São Paulo, Brazil.
Fernanda Aparecida MaggiDivision of General Neurology and Ataxia Unit, Department of Neurology, Federal University of São Paulo - UNIFESP, São Paulo, Brazil.
Vitor TumasMovement Disorders and Behavioral Neurology Section, Ribeirão Preto Medical School, São Paulo University, Ribeirão Preto, Brazil.
Pedro Manzke de CarvalhoMovement Disorders and Behavioral Neurology Section, Ribeirão Preto Medical School, São Paulo University, Ribeirão Preto, Brazil.
Ana Carolina de OliveiraDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Bárbara BragaDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Laura Cristina SouzaDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Rachel Paes GuimarãesDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Luiza Gonzaga PiovesanaDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Íscia Teresinha Lopes-CendesDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Paula Christina de AzevedoDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Marcondes Cavalcante FrançaDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Alberto Rolim Muro MartinezDepartments of Neurology and Medical Genetics, School of Medical Sciences, State University of Campinas, Campinas, Brazil.
Hélio A G TeiveMovement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de clínicas, Federal University of Paraná, Curitiba, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal do Paraná · BRUniversidade Federal de São Paulo · BRHospital de Clínicas Universidade Federal do Paraná · BRUniversidade Vila Velha · BR
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
ataxiacerebellumchoreaHuntington (disease)polyglutamine (polyQ) diseases
Identifiers
What OpenQuestion holds
Textmetadata
LicenceCC BY
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.