Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Movement disorders in hereditary spastic paraplegias.

Arquivos de neuro-psiquiatria - 1 Nov 2023

Pedroso Jose Luiz, Vale Thiago Cardoso, Freitas Julian Letícia de, Araújo Filipe Miranda Milagres, Meira Alex Tiburtino, Neto Pedro Braga, França Marcondes C, Tumas Vitor, Teive Hélio A G, Barsottini Orlando G P

Abstract excerpt

BACKGROUND: Hereditary or familial spastic paraplegias (SPG) comprise a group of genetically and phenotypically heterogeneous diseases characterized by progressive degeneration of the corticospinal tracts. The complicated forms evolve with other various neurological signs and symptoms, including movement disorders and ataxia. OBJECTIVE: To summarize the clinical descriptions of SPG that manifest with movement...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Ataxia
Share to Dystonia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Movement Disorders

Share to Mutation

Share to Parkinsonian Disorders

Share to Proteins

Share to Spastic Paraplegia, Hereditary

Share to Tremor

Source

Open in PubMed Open full text

Identifiers

PMID: 38035585
DOI: 10.1055/s-0043-1777005
PMCID: PMC10689114

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Movement disorders in hereditary spastic paraplegias.PMID 38035585Read ↗

Spastic Paraplegia Type 7 and Movement Disorders: Beyond the Spastic ParaplegiaSemantic proximity Read ↗

Hereditary spastic paraplegia.Semantic proximity Read ↗

Genetics of hereditary spastic paraplegias.Semantic proximity Read ↗

Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with SPG7.Semantic proximity Read ↗

Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive OverviewSemantic proximity Read ↗

Clinical features and management of hereditary spastic paraplegia.Semantic proximity Read ↗

Hereditary Spastic Paraplegia: An Update.Semantic proximity Read ↗

Hereditary spastic paraplegia: new insights into clinical variability and spasticity-ataxia phenotype, and novel mutations.Semantic proximity Read ↗

Hereditary spastic paraplegia: More than an upper motor neuron disease.Semantic proximity Read ↗

Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis.Semantic proximity Read ↗

Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still counting.Semantic proximity Read ↗

Childhood-onset hereditary spastic paraplegia and its treatable mimics.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.