Huntington's disease (HD) is a rare hereditary autosomal dominant neurodegenerative
disorder, which is caused by expression of mutant huntingtin protein (mHTT) with an …

Purinergic receptors (Rs) of the ATP/ADP, UTP/UDP (P2X, P2Y) and adenosine (A1, A2A)-
sensitive classes broadly interfere with cognitive processes both under quasi normal and …

Neurodegenerative disorders are heterogeneous, debilitating, and incurable groups of brain
disorders that have common features including progressive degeneration of the structure …

Huntington's disease (HD) is a neurodegenerative disorder, characterized by motor
dysfunction, psychiatric disturbance, and cognitive decline. In the early stage of HD, occurs a …

Huntington's disease (HD) is a progressive neurodegenerative disease characterized by
neuropsychiatric disturbance, cognitive impairment, and locomotor dysfunction. In the early …

Huntington's disease (HD) is a devastating, progressive, and fatal neurodegenerative
disorder inherited in an autosomal dominant manner. This condition is characterized by …

Neurodegenerative diseases encompass a wide range of debilitating and incurable brain
disorders characterized by the progressive deterioration of the nervous system's structure …

Background and purpose Huntington's disease (HD) is an autosomal dominant condition
caused by CAG‐triplet repeat expansions. CAG‐triplet repeat expansion is inversely …

HTT full‐penetrance pathogenic repeat expansions, the genetic cause of Huntington's
disease (HD), have been recently reported in a minority of frontotemporal …

The inexorable progression of neurodegenerative diseases (NDs), including Alzheimer's
disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and …