Huntington, Susan, 1791-1823. : Memoirs of the late Mrs. Susan Huntington, of Boston, Massachusets : consisting principally of extracts from her journal and letters, with the sermon occasioned by her death / [edited] by Benjamin B. Wisner
1828
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Utah -- Huntington : Goodbye to Poplarhaven : recollections of a Utah boyhood / by Edward A. Geary ; with illustrations by Ralph H. Reynolds
1985
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Huntington (Utah) -- Biography : Goodbye to Poplarhaven : recollections of a Utah boyhood / by Edward A. Geary ; with illustrations by Ralph H. Reynolds
A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)
Huntington's disease -- Pathogenesis : Molecular mechanisms involved in the pathogenesis of Huntington's disease / Claudia Perandones, Federico Eduardo Micheli and Martín Radrizzani
2010
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Huntington's disease -- Pathophysiology : Neurobiology of Huntington's disease : applications to drug discovery / edited by Donald C. Lo and Robert E. Hughes
