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

Phenotype- and genotype-specific structural alterations in spasmodic dysphonia.

Movement disorders : official journal of the Movement Disorder Society - 1 Apr 2017

Bianchi Serena, Battistella Giovanni, Huddleston Hailey, Scharf Rebecca, Fleysher Lazar, Rumbach Anna F, Frucht Steven J, Blitzer Andrew, Ozelius Laurie J, Simonyan Kristina

Abstract excerpt

BACKGROUND: Spasmodic dysphonia is a focal dystonia characterized by involuntary spasms in the laryngeal muscles that occur selectively during speaking. Although hereditary trends have been reported in up to 16% of patients, the causative etiology of spasmodic dysphonia is unclear, and the influences of various phenotypes and genotypes on disorder pathophysiology are poorly understood. In this study, we examined...

Read the complete abstract on PubMed

Topics

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

Share to Anisotropy
Share to Apoptosis Regulatory Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Brain Mapping

Share to Cerebral Cortex

Share to Diffusion Tensor Imaging

Share to GTP-Binding Protein alpha Subunits

Share to Image Processing, Computer-Assisted

Share to Tubulin

Source

Open in PubMed Open full text

Identifiers

PMID: 28186656
DOI: 10.1002/mds.26920
PMCID: PMC5578762

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotype- and genotype-specific structural alterations in spasmodic dysphonia.PMID 28186656Read ↗

Cortical sensorimotor alterations classify clinical phenotype and putative genotype of spasmodic dysphonia.Semantic proximity Read ↗

Polygenic Risk of Spasmodic Dysphonia is Associated With Vulnerable Sensorimotor Connectivity.Semantic proximity Read ↗

Neural correlates of abnormal sensory discrimination in laryngeal dystonia.Semantic proximity Read ↗

Consideration of genetic contributions to the risk for spasmodic dysphonia.Semantic proximity Read ↗

White and grey matter abnormalities in patients withSPG11mutationsSemantic proximity Read ↗

Phenomenology, genetics, and CNS network abnormalities in laryngeal dystonia: A 30-year experience.Semantic proximity Read ↗

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

Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage.Semantic proximity Read ↗

Monozygotic twins with a new compound heterozygous SPG11 mutation and different disease expression.Semantic proximity Read ↗

Multiparametric MRI study of ALS stratified for the C9orf72 genotype.Semantic proximity Read ↗

Thalamocortical Connectivity Correlates with Phenotypic Variability in Dystonia.Semantic proximity Read ↗

Structural white matter abnormalities in patients with idiopathic dystonia.Semantic proximity Read ↗

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