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

SJ Tabrizi, DR Langbehn, BR Leavitt… - The Lancet …, 2009 - thelancet.com
Background Huntington's disease (HD) is an autosomal dominant, fully penetrant,
neurodegenerative disease that most commonly affects adults in mid-life. Our aim was to …

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data

SJ Tabrizi, R Reilmann, RAC Roos, A Durr… - The Lancet …, 2012 - thelancet.com
Background TRACK-HD is a prospective observational biomarker study in premanifest and
early Huntington's disease (HD). In this report we define a battery of potential outcome …

Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis

SJ Tabrizi, RI Scahill, A Durr, RAC Roos… - The Lancet …, 2011 - thelancet.com
Background TRACK-HD is a prospective observational study of Huntington's disease (HD)
that examines disease progression in premanifest individuals carrying the mutant HTT gene …

Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month …

SJ Tabrizi, RI Scahill, G Owen, A Durr… - The Lancet …, 2013 - thelancet.com
Background TRACK-HD is a multinational prospective observational study of Huntington's
disease (HD) that examines clinical and biological findings of disease progression in …

Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional analysis

RI Scahill, P Zeun, K Osborne-Crowley… - The Lancet …, 2020 - thelancet.com
Background Disease-modifying treatments are in development for Huntington's disease;
crucial to their success is to identify a timepoint in a patient's life when there is a measurable …

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

DJH Moss, AF Pardiñas, D Langbehn, K Lo… - The Lancet …, 2017 - thelancet.com
Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin
gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis …

Clinical and biomarker changes in premanifest Huntington disease show trial feasibility: a decade of the PREDICT-HD study

JS Paulsen, JD Long, HJ Johnson… - Frontiers in aging …, 2014 - frontiersin.org
There is growing consensus that intervention and treatment of Huntington disease (HD)
should occur at the earliest stage possible. Various early-intervention methods for this fatal …

Clinical impairment in premanifest and early Huntington's disease is associated with regionally specific atrophy

RI Scahill, NZ Hobbs, MJ Say, N Bechtel… - Human brain …, 2013 - Wiley Online Library
TRACK‐HD is a multicentre longitudinal observational study investigating the use of clinical
assessments and 3‐Tesla magnetic resonance imaging as potential biomarkers for future …

Development of biomarkers for Huntington's disease

DW Weir, A Sturrock, BR Leavitt - The Lancet Neurology, 2011 - thelancet.com
Huntington's disease is an autosomal dominant, progressive neurodegenerative disorder,
for which there is no disease-modifying treatment. By use of predictive genetic testing, it is …

Huntington's disease: from molecular pathogenesis to clinical treatment

CA Ross, SJ Tabrizi - The Lancet Neurology, 2011 - thelancet.com
Huntington's disease is a progressive, fatal, neurodegenerative disorder caused by an
expanded CAG repeat in the huntingtin gene, which encodes an abnormally long …