Sparing of acetylcholinesterase-containing striatal neurons in Huntington's disease

[1]  Joseph B. Martin,et al.  A detailed examination of substance P in pathologically graded cases of Huntington's disease , 1988, Journal of the Neurological Sciences.

[2]  M. Difiglia Synaptic organization of cholinergic neurons in the monkey neostriatum , 1987, The Journal of comparative neurology.

[3]  Joseph B. Martin,et al.  Morphologic and Histochemical Characteristics of a Spared Subset of Striatal Neurons in Huntington's Disease , 1987, Journal of neuropathology and experimental neurology.

[4]  Joseph B. Martin,et al.  Topography of enkephalin, substance P and acetylcholinesterase staining in Huntington's disease striatum , 1986, Neuroscience Letters.

[5]  D. Choi,et al.  Neurons containing NADPH-diaphorase are selectively resistant to quinolinate toxicity. , 1986, Science.

[6]  Joseph B. Martin,et al.  Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid , 1986, Nature.

[7]  J. B. Martin,et al.  Selective sparing of a class of striatal neurons in Huntington's disease. , 1985, Science.

[8]  R. Ferrante,et al.  Neuropathological Classification of Huntington's Disease , 1985, Journal of neuropathology and experimental neurology.

[9]  R. Schwarcz,et al.  Effects of intracerebral injections of quinolinic acid on serotonergic neurons in the rat brain , 1985, Brain Research.

[10]  J. E. Vaughn,et al.  Immunocytochemical localization of choline acetyltransferase within the rat neostriatum: A correlated light and electron microscopic study of cholinergic neurons and synapses , 1985, The Journal of comparative neurology.

[11]  G. Graveland,et al.  Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease. , 1985, Science.

[12]  Joseph B. Martin Huntington's disease , 1984, Neurology.

[13]  A. D. Smith,et al.  The section-Golgi-impregnation procedure—3. Combination of Golgi-impregnation with enzyme histochemistry and electron microscopy to characterize acetylcholinesterase-containing neurons in the rat neostriatum , 1984, Neuroscience.

[14]  A. Parent,et al.  The occurrence of large acetylcholinesterase-containing neurons in human neostriatum as disclosed in normal and Alzheimer-diseased brains , 1984, Brain Research.

[15]  M. Mesulam,et al.  Co-localization of acetylcholinesterase and choline acetyltransferase in the rat cerebrum , 1983, Neuroscience.

[16]  H. Fibiger,et al.  Histochemical demonstration of separate populations of somatostatin and cholinergic neurons in the rat striatum , 1983, Neuroscience Letters.

[17]  R. Schwarcz,et al.  Quinolinic acid: an endogenous metabolite that produces axon-sparing lesions in rat brain. , 1983, Science.

[18]  Z. Henderson Ultrastructure and acetylcholinesterase content of neurones forming connections between the striatum and substantia nigra of rat , 1981, The Journal of comparative neurology.

[19]  E. Spokes,et al.  Neurochemical alterations in Huntington's chorea: a study of post-mortem brain tissue. , 1980, Brain : a journal of neurology.

[20]  L. Butcher,et al.  The localization of acetylcholinesterase in the corpus striatum and substantia nigra of the rat following kainic acid lesion of the corpus striatum: A biochemical and histochemical study , 1979, Neuroscience.

[21]  H. Fibiger,et al.  ACETYLCHOLINESTERASE IN THE SUBSTANTIA NIGRA AND CAUDATE‐PUTAMEN OF THE RAT: PROPERTIES AND LOCALIZATION IN DOPAMINERGIC NEURONS , 1978, Journal of neurochemistry.

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

[23]  K. F. Schroeder,et al.  Morphometric studies of the neuropathological changes in choreatic diseases , 1976, Journal of the Neurological Sciences.

[24]  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.

[25]  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.

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

[27]  T. Powell,et al.  The site of termination of afferent fibres in the caudate nucleus. , 1971, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[28]  F. Fonnum,et al.  Radiochemical micro assays for the determination of choline acetyltransferase and acetylcholinesterase activities. , 1969, The Biochemical journal.