Huntingdon (England) -- Genealogy. : The visitation of the county of Huntingdon, under the authority of William Camden, Clarenceux king of arms, by his deputy, Nicholas Charles, Lancaster herald, A.D. MDCXIII / edited by Sir Henry Ellis
1849
1
Huntingdon gleaner. : Voice of the vanishing minority : Robert Sellar and the Huntingdon Gleaner, 1863-1919 / Robert Hill
Visitations, Heraldic -- England -- Huntingdon. : The visitation of the county of Huntingdon, under the authority of William Camden, Clarenceux king of arms, by his deputy, Nicholas Charles, Lancaster herald, A.D. MDCXIII / edited by Sir Henry Ellis
Huntingdonshire (England) -- Description and travel. : History, gazetteer and directory of the County of Huntingdon : comprising a general survey of the County; and embracing separate historical description of the united Boroughs of Huntingdon and Godmanchester .
1854
1
Huntingdonshire (England) -- Directories. : History, gazetteer and directory of the County of Huntingdon : comprising a general survey of the County; and embracing separate historical description of the united Boroughs of Huntingdon and Godmanchester .
1854
1
Huntingdonshire (England) -- Gazetteers. : History, gazetteer and directory of the County of Huntingdon : comprising a general survey of the County; and embracing separate historical description of the united Boroughs of Huntingdon and Godmanchester .
Huntingdonshire (England) -- History. : History, gazetteer and directory of the County of Huntingdon : comprising a general survey of the County; and embracing separate historical description of the united Boroughs of Huntingdon and Godmanchester .
1854
1
Heraldry -- England -- Huntingdonshire. : The visitation of the county of Huntingdon, under the authority of William Camden, Clarenceux king of arms, by his deputy, Nicholas Charles, Lancaster herald, A.D. MDCXIII / edited by Sir Henry Ellis
1849
1
Visitations, Heraldic -- England -- Huntingdonshire. : The visitation of the county of Huntingdon, under the authority of William Camden, Clarenceux king of arms, by his deputy, Nicholas Charles, Lancaster herald, A.D. MDCXIII / edited by Sir Henry Ellis
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)
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Huntington Disease -- drug therapy : Neurobiology of Huntington's disease : applications to drug discovery / edited by Donald C. Lo and Robert E. Hughes
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)
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)
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)
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Huntington Disease -- nursing. : Caring for persons with Huntington's disease : a handbook for health care professionals / editor, Edmond Chiu
