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

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.

Annals of neurology - 1 Feb 1996

Gilman S, Sima A A, Junck L, Kluin K J, Koeppe R A, Lohman M E, Little R

Abstract excerpt

Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited progressive neurological disorder characterized by neuronal degeneration and reactive gliosis in the cerebellum, brainstem, spinocerebellar tracts, and dorsal columns. Multiple system atrophy is a sporadic progressive neurological dis...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Aged, 80 and over
Share to Brain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunohistochemistry

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Pedigree

Share to Reference Values

Source

Identifiers

PMID: 8967756
DOI: 10.1002/ana.410390214

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-8967756-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.PMID 8967756Read ↗

Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.Semantic proximity Read ↗

Heterogeneity of Multiple System Atrophy: An UpdateSemantic proximity Read ↗

PET and MRI reveal early evidence of neurodegeneration in spinocerebellar ataxia type 17.Semantic proximity Read ↗

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.Semantic proximity Read ↗

Florzolotau (18F) PET provides in-vivo measures of tau pathology in progressive supranuclear palsy: An imaging-postmortem correlation studySemantic proximity Read ↗

Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.Semantic proximity Read ↗

Novel Imaging Phenotype in Spinal Cerebellar Ataxia Type 8: Symmetrical White Matter Changes without Cerebellar Atrophy.Semantic proximity Read ↗

The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.Semantic proximity Read ↗

Differential value of brain magnetic resonance imaging in multiple system atrophy cerebellar phenotype and spinocerebellar ataxias.Semantic proximity Read ↗

Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases.Semantic proximity Read ↗

BIOLOGICAL SCIENCES: Neuroscience, cell biology MTSS1/Src family kinase Dysregulation Underlies Multiple Inherited AtaxiasSemantic proximity Read ↗

Should genetic testing for SCAs be included in the diagnostic workup for MSA?Semantic proximity Read ↗

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