Huntington's disease (HD) is a fully penetrant neurodegenerative disease caused by a
dominantly inherited CAG trinucleotide repeat expansion in the huntingtin gene on …

Huntington's disease (HD) is a devastating inherited neurodegenerative disease
characterized primarily by progressive motor, cognitive, and psychiatric symptoms. It is …

Huntington's disease (HD) is an autosomal neurodegenerative disease that is characterized
by an excessive number of CAG trinucleotide repeats within the huntingtin gene (HTT). HD …

Pathophysiology of Huntington's disease: from huntingtin fun... : Current Opinion in Neurology
Pathophysiology of Huntington's disease: from huntingtin functions to potential treatments …

Huntington's disease (HD) is an inherited neurodegenerative disease characterised by
neuropsychiatric symptoms, a movement disorder (most commonly choreiform) and …

Huntington disease is devastating to patients and their families—with autosomal dominant
inheritance, onset typically in the prime of adult life, progressive course, and a combination …

Huntington disease is a monogenic neurodegenerative disorder that displays an autosomal-
dominant pattern of inheritance. It is characterized by motor, psychiatric, and cognitive …

Huntington's disease is an autosomal dominantly inherited progressive neurodegenerative
disorder. The mutant gene has been localised to chromosome 4p16. 3. The gene product …

Abstract Purpose of Review This article describes and discusses new potential disease-
modifying therapies for Huntington's disease that are currently in human clinical trials as well …

Huntington's disease (HD) is a neurodegenerative disorder that usually starts in middle age
and is characterized by involuntary movements (chorea), personality changes and …