Huntington's disease (HD) is an autosomal dominant disorder caused by a tandem repeat expansion encoding an expanded tract of glutamines in the huntingtin protein. HD is progressive and manifests as psychiatric symptoms (including depression), cognitive deficits (culminating in dementia), and motor abnormalities (including chorea). Having reached the twentieth anniversary of the discovery of the "genetic stutter" which causes HD, we still lack sophisticated insight into why so many HD patients exhibit affective disorders such as depression at very early stages, prior to overt appearance of motor deficits. In this review, we will focus on depression as the major psychiatric manifestation of HD, discuss potential mechanisms of pathogenesis id...
ObjectiveAlthough Huntington disease (HD) is caused by an autosomal dominant mutation, its phenotypi...
Presymptomatic individuals with the Huntingtin (HTT) CAG expansion mutation that causes Huntington’s...
Objective: Although Huntington disease (HD) is caused by an autosomal dominant mutation, its phenoty...
Huntington’s disease (HD) is an autosomal dominant disorder caused by a tandem repeat expansion enco...
© 2008 Dr. Terence Yeow-Chwen PangHuntington’s disease (HD) is an inherited neurodegenerative disord...
Huntington disease is a neurodegenerative disorder caused by an expanded CAG repeat in the Huntingto...
Huntington’s disease (HD) is a neurodegenerative disorder that is best known for its effect on motor...
© 2012 Dr. Xin DuOf the plethora of symptoms that arise in HD, depression is the most diagnosed psyc...
Psychiatric symptoms such as depression and anxiety are important clinical features of Huntingtons d...
BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expand...
Contains fulltext : 181922.pdf (publisher's version ) (Open Access)Huntington dise...
Huntington’s disease is an autosomal-dominant disease characterized by deterioration in motor, cogni...
International audienceBackground: In Huntington’s disease psychiatric symptoms may manifest prior to...
Non-motor symptoms and signs such as metabolic and psychiatric disturbances have been reported to oc...
Huntington’s disease (HD) is a neurodegenerative disorder caused by a tandem repeat expansion encodi...
ObjectiveAlthough Huntington disease (HD) is caused by an autosomal dominant mutation, its phenotypi...
Presymptomatic individuals with the Huntingtin (HTT) CAG expansion mutation that causes Huntington’s...
Objective: Although Huntington disease (HD) is caused by an autosomal dominant mutation, its phenoty...
Huntington’s disease (HD) is an autosomal dominant disorder caused by a tandem repeat expansion enco...
© 2008 Dr. Terence Yeow-Chwen PangHuntington’s disease (HD) is an inherited neurodegenerative disord...
Huntington disease is a neurodegenerative disorder caused by an expanded CAG repeat in the Huntingto...
Huntington’s disease (HD) is a neurodegenerative disorder that is best known for its effect on motor...
© 2012 Dr. Xin DuOf the plethora of symptoms that arise in HD, depression is the most diagnosed psyc...
Psychiatric symptoms such as depression and anxiety are important clinical features of Huntingtons d...
BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an expand...
Contains fulltext : 181922.pdf (publisher's version ) (Open Access)Huntington dise...
Huntington’s disease is an autosomal-dominant disease characterized by deterioration in motor, cogni...
International audienceBackground: In Huntington’s disease psychiatric symptoms may manifest prior to...
Non-motor symptoms and signs such as metabolic and psychiatric disturbances have been reported to oc...
Huntington’s disease (HD) is a neurodegenerative disorder caused by a tandem repeat expansion encodi...
ObjectiveAlthough Huntington disease (HD) is caused by an autosomal dominant mutation, its phenotypi...
Presymptomatic individuals with the Huntingtin (HTT) CAG expansion mutation that causes Huntington’s...
Objective: Although Huntington disease (HD) is caused by an autosomal dominant mutation, its phenoty...