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

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

Cerebellum (London, England) - 1 Jun 2020

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

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Brazil
Share to Intellectual Disability
Share to Morocco
Share to Muscle Spasticity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nuclear Pore Complex Proteins

Share to Optic Atrophy

Share to Spastic Paraplegia, Hereditary

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 32146693
DOI: 10.1007/s12311-020-01123-9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neurological Phenotypes Associated with AAAS-Related Disorders: Spastic Ataxia and Complex Spastic Paraplegia.PMID 32146693Read ↗

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

Reviewing the genetic causes of spastic-ataxias.Semantic proximity Read ↗

A Diagnostic Approach to Spastic ataxia Syndromes.Semantic proximity Read ↗

Genetic ataxias: update on classification and diagnostic approaches.Semantic proximity Read ↗

Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder.Semantic proximity Read ↗

Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆.Semantic proximity Read ↗

Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrum.Semantic proximity Read ↗

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

[Ataxias and hereditary spastic paraplegias].Semantic proximity Read ↗

[AAA ATPases and hereditary spastic paraplegia].Semantic proximity Read ↗

A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy.Semantic proximity Read ↗

Revisiting genotype-phenotype overlap in neurogenetics: triplet-repeat expansions mimicking spastic paraplegias.Semantic proximity Read ↗

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