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

Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia.

Neurology - 1 Oct 1996

Greenstein P E, Moore D, Levy-Lohad E, Stephens K, Bird T D

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 Genotype
Share to Machado-Joseph Disease
Share to Phenotype
Share to Spinocerebellar Degenerations

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8857759
DOI: 10.1212/wnl.47.4.1106-a

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nine families with the SCA3/Machado-Joseph disease type of inherited ataxia.PMID 8857759Read ↗

Machado Joseph disease: clinical and genetic aspects, and current treatmentSemantic proximity Read ↗

Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3.Semantic proximity Read ↗

[Recent advances in molecular genetics of spinocerebellar ataxia type 3/Machado-Joseph disease].Semantic proximity Read ↗

Machado-Joseph Disease: from first descriptions to new perspectives.Semantic proximity Read ↗

SCA3: Neurological features, pathogenesis and animal modelsSemantic proximity Read ↗

[Overview of Hereditary Spinocerebellar Ataxias in Japan].Semantic proximity Read ↗

Spinocerebellar Ataxia type 3 is rare in the Peruvian PopulationSemantic proximity Read ↗

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.Semantic proximity Read ↗

Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1.Semantic proximity Read ↗

Polyglutamine diseases: The special case of ataxin-3 and Machado–Joseph diseaseSemantic proximity Read ↗

Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature reviewSemantic proximity Read ↗

Spinocerebellar ataxia type 3: subphenotypes in a cohort of Brazilian patients.Semantic proximity Read ↗

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