Huntington's disease (HD) is a chronic neurodegenerative disorder caused by an expansion
of polyglutamine repeats in exon 1 of the Huntingtin gene. Transcriptional dysregulation …

Hereditary Huntington's disease (HD) is characterized by cell dysfunction and death in the
brain, leading to progressive cognitive, psychiatric, and motor impairments. Despite …

We used behavioral testing and morphological methods to detail the progression of basal
ganglia neuron type‐specific pathology and the deficits stemming from them in male …

Huntington's disease (HD) is a rare, autosomal neurodegenerative disease characterized by
motor and cognitive impairments appearing in adults. The R6/1 mouse model of the disease …

Background and purpose Different amounts of cumulative exposure to the toxic mutant form
of the huntingtin protein might underlie the distinctive pattern of striatal connectivity in pre …

Huntington's disease (HD) is a neurodegenerative disorder that presents motor, cognitive
and psychiatric symptoms as it progresses. Prior to motor symptoms onset, alterations and …

[eng] Huntington's Disease (HD) is an autosomal dominant inherited neurodegenerative
disorder characterized by motor, psychiatric, and cognitive manifestations. The disease is …

2 oder psychotischen Episoden, Depressionen oder Suizidalität kommen (Kipps et al., 2005;
Rosas et al., 2002; Jenkins et al., 1998; Albin, 1995; Albin et al., 1992). Aufgrund der …

Huntington's disease (HD) is a genetic neurodegenerative disease caused by an expanded
CAG-repeat mutation in exon 1 of the gene encoding huntingtin (HTT) which results in an …

Beyond the motor impairment, Parkinson's disease (PD) is also characterised by an early
appearance of psychiatric symptoms such as apathy, depression and cognitive deficits …