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

Familial striatal degeneration: New mutation and neuroimaging clues.

Neurology - 17 Nov 2015

Barsottini Orlando Graziani Povoas, Martins Pedro de Miranda, Chien Hsin Fen, Raskin Salmo, Nunes Renato Hoffmann, da Rocha Antônio José, Pedroso José Luiz

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 3',5'-Cyclic-AMP Phosphodiesterases
Share to Machado-Joseph Disease
Share to Mutation
Share to Neuroimaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 26475694
DOI: 10.1212/WNL.0000000000002128

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial striatal degeneration: New mutation and neuroimaging clues.PMID 26475694Read ↗

Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disordersSemantic proximity Read ↗

Neuropathology of hereditary forms of frontotemporal dementia and parkinsonism.Semantic proximity Read ↗

A case report of adult-onset Alexander disease clinically presenting as Parkinson's disease: is the comorbidity associated with genetic susceptibility?Semantic proximity Read ↗

"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.Semantic proximity Read ↗

Progressive Supranuclear Palsy: an Update.Semantic proximity Read ↗

Novel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification.Semantic proximity Read ↗

Juvenile parkinsonism: Differential diagnosis, genetics, and treatmentSemantic proximity Read ↗

Hereditary neuropathies in childhood: morphologic hallmarks and pathophysiologic mechanisms.Semantic proximity Read ↗

Absence of Lewy pathology associated with PINK1 homozygous mutation.Semantic proximity Read ↗

Parkinsonism phenotype in a family with adult onset Alexander disease and a novel mutation of GFAP.Semantic proximity Read ↗

Twinkle-associated familial parkinsonism with Lewy pathology: Cause or predisposition?Semantic proximity Read ↗

Clinical features of Wolff-Parkinson-White syndromeSemantic proximity Read ↗

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