Huntington's disease (HD) is a neurodegenerative disease caused by the expansion of unstable CAG repeats in the HTT gene. There are scarce data about HD in China. Fifty-eight HD patients were consecutively recruited and assessed using the Unified HD Rating Scale (UHDRS) motor section and UHDRS behaviour assessment (UHDRS-b). Genetic analyses were also conducted. Thirty-three women and Twenty -five men were diagnosed with a mean age of 46.1 ± 11.2 years and a mean number of CAG triplet repeats 44.6 ± 4.4. CAG triplet repeat number was negatively correlated with age at onset, and positively correlated with UHDRS-b total score, and its subdomains including depressed mood, low self-esteem, anxiety and irritability. On the other hand, negative c...
Objective: There is controversy about the clinical consequences of intermediate alleles (IAs) in Hun...
HuntingtonÕs Disease (HD) is a late-onset and progressive neurodegenerative disease of the central n...
Huntington disease (HD) is an autosomal-dominant disorder that results from 36 CAG repeats in the HD...
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
Huntington’s disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
To understand the clinical and genetic features of Huntington disease (HD).The clinical data of HD c...
Background: Knowledge about HD in China is lacking in the international literature. We have therefor...
Huntington’s disease (HD) is a rare neurodegenerative disorder with autosomal dominant inheritance, ...
Clinical data across the globe especially in genetic diseases like Huntington’s disease (HD) is most...
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
Objective Huntington's disease (HD) is a genetic neurodegenerative disease characterized by cognitiv...
We studied the expanded CAG repeat and adjacent CCG repeat in 53 Huntington's disease (HD) patients ...
BACKGROUND: Huntington's disease (HD) is a rare triplet repeat (CAG) disorder. Advanced, multi-c...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
Objective: The objective was to review the major differences of Huntington disease (HD) in Asian pop...
Objective: There is controversy about the clinical consequences of intermediate alleles (IAs) in Hun...
HuntingtonÕs Disease (HD) is a late-onset and progressive neurodegenerative disease of the central n...
Huntington disease (HD) is an autosomal-dominant disorder that results from 36 CAG repeats in the HD...
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
Huntington’s disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
To understand the clinical and genetic features of Huntington disease (HD).The clinical data of HD c...
Background: Knowledge about HD in China is lacking in the international literature. We have therefor...
Huntington’s disease (HD) is a rare neurodegenerative disorder with autosomal dominant inheritance, ...
Clinical data across the globe especially in genetic diseases like Huntington’s disease (HD) is most...
Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CA...
Objective Huntington's disease (HD) is a genetic neurodegenerative disease characterized by cognitiv...
We studied the expanded CAG repeat and adjacent CCG repeat in 53 Huntington's disease (HD) patients ...
BACKGROUND: Huntington's disease (HD) is a rare triplet repeat (CAG) disorder. Advanced, multi-c...
Careful characterization of the phenotype and genotype of Huntington disease (HD) can foster better ...
Objective: The objective was to review the major differences of Huntington disease (HD) in Asian pop...
Objective: There is controversy about the clinical consequences of intermediate alleles (IAs) in Hun...
HuntingtonÕs Disease (HD) is a late-onset and progressive neurodegenerative disease of the central n...
Huntington disease (HD) is an autosomal-dominant disorder that results from 36 CAG repeats in the HD...