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

Motor outcome measures in Huntington disease clinical trials.

Handbook of clinical neurology - 1 Jan 2017

Reilmann Ralf, Schubert Robin

Abstract excerpt

Deficits in motor function are a hallmark of Huntington disease (HD). The Unified Huntington's Disease Rating Scale Total Motor Score (UHDRS-TMS) is a categoric clinical rating scale assessing multiple domains of motor disability in HD. The UHDRS-TMS or subsets of its items have served as primary or secondary endpoints in numerous clinical trials. In spite of a well-established video-based annual online...

Read the complete abstract on PubMed

Topics

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

Share to Outcome Assessment, Health Care
Share to Phenotype
Share to Clinical Trials as Topic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cross-Sectional Studies

Share to Huntington Disease

Share to Reproducibility of Results

Share to Sensitivity and Specificity

Source

Identifiers

PMID: 28947119
DOI: 10.1016/B978-0-12-801893-4.00018-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Motor outcome measures in Huntington disease clinical trials.PMID 28947119Read ↗

A biological classification of Huntington's disease: the Integrated Staging System.Semantic proximity Read ↗

Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data.Semantic proximity Read ↗

Evaluating motor progression of juvenile-onset Huntington's Disease: An Enroll-HD analysis.Semantic proximity Read ↗

Objective assessment of gait and posture in premanifest and manifest Huntington disease - A multi-center study.Semantic proximity Read ↗

Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials.Semantic proximity Read ↗

Differentiating Hyperkinetic and Hypokinetic Motor Features in the Progression of Huntington’s DiseaseSemantic proximity Read ↗

Influence of Age of Onset on Huntington's Disease Phenotype.Semantic proximity Read ↗

Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease.Semantic proximity Read ↗

Modeling disease progression and placebo response in Huntington's Disease: Insights from Enroll-HD and GENERATION HD1 cohortsSemantic proximity Read ↗

Tracking motor impairments in the progression of Huntington's disease.Semantic proximity Read ↗

Identification of extreme motor phenotypes in Huntington's disease.Semantic proximity Read ↗

Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational data.Semantic proximity Read ↗

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