Seven cases of huntington's disease in childhood and levodopa induced improvement in the hypokinetic — Rigid form

[1]  G. Bruyn,et al.  [Huntington's chorea]. , 1964 .

[2]  C. Cianchetti,et al.  Apomorphine hydrochloride-induced improvement in Huntington's chorea: stimulation of dopamine receptor. , 1978, Archives of neurology.

[3]  M. Trabucchi,et al.  Bromocriptine and Huntington's chorea. , 1978, Archives of neurology.

[4]  M. Hayden,et al.  IMPAIRED PROLACTIN RELEASE IN HUNTINGTON'S CHOREA EVIDENCE FOR DOPAMINERGIC EXCESS , 1977, The Lancet.

[5]  P. Spano,et al.  TREATMENT OF HUNTINGTON'S CHOREA WITH BROMOCRIPTINE , 1977, Acta neurologica Scandinavica.

[6]  R. Spreafico,et al.  Biochemical aspects of Huntington's chorea. , 1977, Journal of neurology, neurosurgery, and psychiatry.

[7]  J. Edwards,et al.  HUNTINGTON'S CHOREA , 1977, The Lancet.

[8]  G. McKhann,et al.  Long‐term treatment of juvenile Huntington's chorea with dipropylacetic acid , 1977, Neurology.

[9]  C. Loeb,et al.  Levodopa and Huntington's chorea , 1976, Journal of neurology, neurosurgery, and psychiatry.

[10]  D. Calne,et al.  BROMOCRIPTINE AND LEVODOPA (WITH OR WITHOUT CARBIDOPA) IN PARKINSONISM , 1976, The Lancet.

[11]  P. Mcgeer,et al.  ENZYMES ASSOCIATED WITH THE METABOLISM OF CATECHOLAMINES, ACETYLCHOLINE AND GABA IN HUMAN CONTROLS AND PATIENTS WITH PARKINSON'S DISEASE AND HUNTINGTON'S CHOREA , 1976, Journal of neurochemistry.

[12]  G. Omenn,et al.  Monozygotic twins with Huntington's disease in a family expressing the rigid variant , 1975, Neurology.

[13]  D. Michaelides The effects of levodopa in chronic progressive hereditary chorea (Huntington's chorea): case report. , 1975, Military medicine.

[14]  S. Aquilonius,et al.  Regional distribution of choline acetyltransferase in the human brain: changes in Huntington's chorea. , 1975, Journal of neurology, neurosurgery, and psychiatry.

[15]  P. Swanson,et al.  Biochemical abnormalities in Huntington's chorea brains , 1974, Neurology.

[16]  T. Chase,et al.  Parkinson disease treated with a suspected dopamine receptor agonist. , 1974, Archives of neurology.

[17]  H. Leijnse-Ybema,et al.  HUNTINGTON'S CHOREA AND LEVODOPA , 1974 .

[18]  D. Mclellan,et al.  A double-blind trial of tetrabenazine, thiopropazate, and placebo in patients with chorea. , 1974, Lancet.

[19]  T. Chase Central monoamine metabolism in man. Effect of putative dopamine receptor agonists and antagonists. , 1973, Archives of neurology.

[20]  H. Fibiger,et al.  Choline acetylase and glutamic acid decarboxylase in Huntington's chorea , 1973, Neurology.

[21]  C. Yates,et al.  Lysosomal enzymes, amino acids and acid metabolites of amines in Huntington's chorea. , 1973, Clinica chimica acta; international journal of clinical chemistry.

[22]  Shirley Hansen,et al.  Huntington's Chorea , 1973 .

[23]  K. Heathfield Huntington's chorea: a centenary review. , 1973, Postgraduate medical journal.

[24]  Allsop Jl,et al.  Huntington's chorea--the rigid form (Westphal variant) treated with l-DOPA: a case report. , 1973 .

[25]  T. Chase,et al.  Central monoamine metabolism in Parkinson's disease. , 1972, Archives of neurology.

[26]  D. Sharpe,et al.  Amine metabolites in the cerebrospinal fluid in Huntington's chorea , 1972 .

[27]  B. Tan,et al.  Levodopa in Huntington's chorea. , 1972, Lancet.

[28]  A. Barbeau L-dopa therapy in Parkinson's disease: a critical review of nine years' experience. , 1969, Canadian Medical Association journal.

[29]  A. Aronson,et al.  Differential diagnostic patterns of dysarthria. , 1969, Journal of speech and hearing research.

[30]  George C. Cotzias,et al.  Modification of Parkinsonism--chronic treatment with L-dopa. , 1969, The New England journal of medicine.

[31]  N. Myrianthopoulos Huntington's Chorea , 1966, Journal of medical genetics.

[32]  O. Hornykiewicz Dopamine (3-hydroxytyramine) and brain function. , 1966, Pharmacological reviews.

[33]  G. Jervis HUNTINGTON'S CHOREA IN CHILDHOOD. , 1963, Archives of neurology.