<p>Values are listed as mean (standard deviation) unless otherwise noted.</p><p>COHORT = Cooperative Huntington Observational Research Trial; HD = Huntington disease; (CAG)<sub>n</sub> = cytosine-adenine-guanine repeat length in the <i>Huntingtin</i> allele; UHDRS = Unified Huntington's Disease Rating Scale.</p><p>*P-values refer to overall tests of heterogeneity across all six groups.</p><p>**For motor and behavioral measures, higher scores reflect greater impairment. For cognitive, independence, and functional measures, higher scores reflect less impairment.</p
BACKGROUND: Understanding the relation between predominantly choreatic and hypokinetic-rigid motor s...
<p>Legend. HD = Huntington's disease; Pre-HD = gene-positive, without motor symptoms; SD = standard ...
Clinical trials to improve day-to-day function in Huntington disease (HD) require accurate outcome m...
<p>Values are listed as mean (standard deviation) unless otherwise noted.</p><p>COHORT = Cooperative...
<p>Data are means±SD (range) or % (n).</p><p>TFC, Total Functional Capacity; UHDRS, Unified Huntingt...
*<p>Chorea subscore 28 maximal, worst, dystonia subscore 20 maximal, worst</p><p>The values represen...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
<p>Note: IQ (NART, National Adult Reading Test); CAG, cytosine-adenine-guanine (number of repeats >4...
<p>Data are expressed as mean±SD (range). UHDRS Part I: Unified Huntington Disease Rating Scale Part...
<p>Values are expressed as means ± SE (range; minimum–maximum).</p><p>UHDRS: The Unified Huntington'...
<p>HD Huntington' disease; SDMT Symbol digit modality test.</p><p>n: available data; Baseline: Mean ...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
Studying individuals with extreme phenotypes could facilitate the understanding of disease modificat...
Background: Composite scores derived from joint statistical modelling of individual risk factors are...
BACKGROUND: Huntington's disease (HD) is an autosomal dominant, fully penetrant, neurodegenerative d...
BACKGROUND: Understanding the relation between predominantly choreatic and hypokinetic-rigid motor s...
<p>Legend. HD = Huntington's disease; Pre-HD = gene-positive, without motor symptoms; SD = standard ...
Clinical trials to improve day-to-day function in Huntington disease (HD) require accurate outcome m...
<p>Values are listed as mean (standard deviation) unless otherwise noted.</p><p>COHORT = Cooperative...
<p>Data are means±SD (range) or % (n).</p><p>TFC, Total Functional Capacity; UHDRS, Unified Huntingt...
*<p>Chorea subscore 28 maximal, worst, dystonia subscore 20 maximal, worst</p><p>The values represen...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
<p>Note: IQ (NART, National Adult Reading Test); CAG, cytosine-adenine-guanine (number of repeats >4...
<p>Data are expressed as mean±SD (range). UHDRS Part I: Unified Huntington Disease Rating Scale Part...
<p>Values are expressed as means ± SE (range; minimum–maximum).</p><p>UHDRS: The Unified Huntington'...
<p>HD Huntington' disease; SDMT Symbol digit modality test.</p><p>n: available data; Baseline: Mean ...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
Studying individuals with extreme phenotypes could facilitate the understanding of disease modificat...
Background: Composite scores derived from joint statistical modelling of individual risk factors are...
BACKGROUND: Huntington's disease (HD) is an autosomal dominant, fully penetrant, neurodegenerative d...
BACKGROUND: Understanding the relation between predominantly choreatic and hypokinetic-rigid motor s...
<p>Legend. HD = Huntington's disease; Pre-HD = gene-positive, without motor symptoms; SD = standard ...
Clinical trials to improve day-to-day function in Huntington disease (HD) require accurate outcome m...