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

Metabolic changes in DYT11 myoclonus-dystonia.

Neurology - 22 Jan 2013

Carbon Maren, Raymond Deborah, Ozelius Laurie, Saunders-Pullman Rachel, Frucht Steven, Dhawan Vijay, Bressman Susan, Eidelberg David

Abstract excerpt

OBJECTIVE: To identify brain regions with metabolic changes in DYT11 myoclonus-dystonia (DYT11-MD) relative to control subjects and to compare metabolic abnormalities in DYT11-MD with those found in other forms of hereditary dystonia and in posthypoxic myoclonus. METHODS: [(18)F]-fluorodeoxyglucose PET was performed in 6 subjects with DYT11-MD (age 30.5 ± 10.1 years) and in 6 nonmanifesting DYT11 mutation...

Read the complete abstract on PubMed

Topics

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

Share to Dystonic Disorders
Share to Fluorodeoxyglucose F18
Share to Parietal Lobe

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

Share to Penetrance

Share to Positron-Emission Tomography

Share to Prefrontal Cortex

Share to Sarcoglycans

Share to Thalamus

Source

Open in PubMed Open full text

Identifiers

PMID: 23284065
DOI: 10.1212/WNL.0b013e31827f0798
PMCID: PMC3589244

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

Metabolic changes in DYT11 myoclonus-dystonia.PMID 23284065Read ↗

Regional metabolism in primary torsion dystonia: effects of penetrance and genotype.Semantic proximity Read ↗

Primary dystonia: is abnormal functional brain architecture linked to genotype?Semantic proximity Read ↗

Functional brain networks in DYT1 dystonia.Semantic proximity Read ↗

Genotype-phenotype interactions in primary dystonias revealed by differential changes in brain structure.Semantic proximity Read ↗

Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia.Semantic proximity Read ↗

Brain of miyoshi myopathy/dysferlinopathy patients presents with structural and metabolic anomalies.Semantic proximity Read ↗

Metabolic and volumetric alterations in the basal ganglia and the cerebellum in dopa-responsive dystonia in symptomatic and asymptomatic <i>GCH1</i> mutation carriersSemantic proximity Read ↗

Striatal and cerebellar vesicular acetylcholine transporter expression is disrupted in human DYT1 dystoniaSemantic proximity Read ↗

Severity of dystonia is correlated with putaminal gray matter changes in myoclonus-dystonia.Semantic proximity Read ↗

Metabolic and Volumetric Alterations in the Basal Ganglia and the Cerebellum in Dopa-Responsive Dystonia in Symptomatic and Asymptomatic GCH1 Mutation Carriers.Semantic proximity Read ↗

Understanding the anatomy of dystonia: determinants of penetrance and phenotype.Semantic proximity Read ↗

Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystoniaSemantic proximity Read ↗

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