Chapter 33 The history of movement disorders
Tài liệu tham khảo
Adams, 1949, The neurological changes in the more common types of severe liver disease, Trans Am Neurol Assoc, 74, 217
Adams, 1953, The neurological disorders associated with liver disease, Res Publ Assoc Res Nerv Ment Dis, 32, 198
Adams, 1964, Striato-nigral degeneration, J Neuropathol Exp Neurol, 23, 584
Albin, 1989, The functional anatomy of basal ganglia disorders, Trends Neurosci, 12, 366, 10.1016/0166-2236(89)90074-X
Albin, 1989, Feline subthalamic nucleus neurons contain glutamate-like but not GABA-like or glycine-like immunoreactivity, Brain Res, 491, 185, 10.1016/0006-8993(89)90103-0
Albin, 1990, Abnormalities of striatal projection neurons and N-methyl-D-aspartate receptors in presymptomatic Huntington's disease, N Engl J Med, 322, 1293, 10.1056/NEJM199005033221807
Albin, 1992, Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington's disease, Ann Neurol, 31, 425, 10.1002/ana.410310412
Alexander, 1986, Parallel organization of functionally segregated circuits linking basal ganglia and cortex, Annu Rev Neurosci, 9, 357, 10.1146/annurev.ne.09.030186.002041
Altenmüller, 2005, 179
Alzheimer A, 1911, Über die anatomische Grundlage der Huntingtonischen Chorea und der choreatischen Bewegungen überhaupt, Z Gesamte Neurol Psychiatr, 3, 566
1998, ACMG/ASHG statement: laboratory guidelines for Huntington disease genetic testing, Am J Hum Genet, 62, 1243, 10.1086/301846
Anden, 1964, Demonstration and mapping out of nigro-neostriatal dopamine neurons, Life Sci, 3, 523, 10.1016/0024-3205(64)90161-4
Anden, 1965, Further evidence for the presence of nigro-striatal dopamine neurons in the rat, Am J Anat, 116, 329, 10.1002/aja.1001160117
Andermann, 1980, Startle disease or hyperekplexia: further delineation of the syndrome, Brain, 103, 985, 10.1093/brain/103.4.985
Andrew, 1993, The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease, Nat Genet, 4, 398, 10.1038/ng0893-398
Arima, 1998, NACP/alpha-synuclein immunoreactivity in fibrillary components of neuronal and oligodendroglial cytoplasmic inclusions in the pontine nuclei in multiple system atrophy, Acta Neuropathol (Berl), 96, 439, 10.1007/s004010050917
Ayd, 1961, A survey of drug-induced extrapyramidal reactions, JAMA, 75, 1054, 10.1001/jama.1961.03040120016004
Aziz, 1991, Lesions of the subthalamic nucleus for the alleviation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced parkinsonism in the primate, Mov Disord, 6, 288, 10.1002/mds.870060404
Barbeau, 1958, The understanding of involuntary movements: an historical approach, J Nerv Ment Dis, 127, 469, 10.1097/00005053-195812000-00001
Barbeau, 1965, Dégénérescence plurisystématisée du nevraxe. Syndrome de Steele–Richardson–Olszewski, Union Med Can, 94, 715
Barbeau, 1970, Parental ascent in the juvenile form of Huntington's chorea, Lancet, 2, 927
Barbeau, 1962, Les catécholamines dans la maladie de Parkinson, 247
Barraquer-Bordas, 1988, Idiopathic torsion dystonia as described by Barraquer-Roviralta, Adv Neurol, 50, 665
Barraquer-Roviralta, 1897, Contribución al estudio de la atetosis, Gac Med Catalana, 20, 385
Beal, 1986, Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid, Nature, 32, 168, 10.1038/321168a0
Beard, 1869, Neurasthenia, or nervous exhaustion, Boston Medical and Surgical Journal, 80, 217, 10.1056/NEJM186904290801301
Beard, 1878, Dr. Beard's verbal communication, J Nerv Ment Dis, 5, 525
Beard, 1880, Experiments with the “jumpers” or “jumping Frenchmen” of Maine, J Nerv Ment Dis, 7, 487
Beard, 1880, Experiments with the “jumpers” of Maine, Popul Sci Monthly, 18, 170
Beard, 1871, 452
Bearn, 1957, Wilson's disease. An inborn error of metabolism with multiple manifestations, Am J Med, 22, 747, 10.1016/0002-9343(57)90125-0
Bearn, 1960, A genetical analysis of 30 families with Wilson's disease (hepatolenticular degeneration), Ann Hum Genet, 24, 33, 10.1111/j.1469-1809.1959.tb01713.x
Bearn, 1952, Biochemical abnormalities in Wilson's disease, J Clin Invest, 31, 616
Bell, 1830, 221
Benabid, 1987, Combined (thalamotomy and stimulation) stereotactic surgery of the VIM thalamic nucleus for bilateral Parkinson's disease, Appl Neurophysiol, 50, 344
Benabid, 1991, Long-term suppression of tremor by chronic stimulation of the ventral intermediate thalamic nucleus, Lancet, 337, 403, 10.1016/0140-6736(91)91175-T
Benabid, 1994, Acute and long-term effects of subthalamic nucleus stimulation in Parkinson's disease, Stereotact Funct Neurosurg, 62, 76, 10.1159/000098600
Benazzouz, 1993, Reversal of rigidity and improvement in motor performance by subthalamic high-frequency stimulation in MPTP-treated monkeys, Eur J Neurosci, 5, 382, 10.1111/j.1460-9568.1993.tb00505.x
Berciano, 1999, An early description of striatonigral degeneration, J Neurol, 246, 462, 10.1007/s004150050384
Bergman, 1990, Reversal of experimental parkinsonism by lesions of the subthalamic nucleus, Science, 249, 1436, 10.1126/science.2402638
Bergman, 1994, The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of Parkinsonism, J Neurophysiol, 72, 507, 10.1152/jn.1994.72.2.507
Bertler, 1959, Occurrence and distribution of catechol amines in brain, Acta Physiol Scand, 47, 350
Birkmayer, 1961, Der L-3,4-Dioxyphenylalanin (=DOPA)-Effekt bei der Parkinson-Akinese, Wien Klin Wochenschr, 73, 787
Blackwood, 1889, Mechanical writing in the prevention and cure of writers' cramp and allied disorders, Medical Register (Philadelphia), 5, 365
Blocq, 1893, Sur un cas de tremblement parkinsonien hémiplégique symptomatique d'une tuneur du peduncle cerebral, Comptes Rendus Hebdomadaires des Séances et Mémoires de la Société de Biologie, 5, 105
Bouteille, 1810
Bramwell, 1916, Familial cirrhosis of the liver: four cases of acute fatal cirrhosis in the same family, the patients being respectively nine, ten, fourteen and fourteen years of age: suggested relationship to Wilson's progressive degeneration of the lenticular nucleus, Edinburgh Med J, 17, 90
Brandt, 1996, Trinucleotide repeat length and clinical progression in Huntington's disease, Neurology, 46, 527, 10.1212/WNL.46.2.527
Brewer, 1983, Oral zinc therapy for Wilson's disease, Ann Intern Med, 99, 314, 10.7326/0003-4819-99-3-314
Brewer, 1998, Treatment of Wilson's disease with zinc. XV. Long-term follow-up studies, J Lab Clin Med, 132, 264, 10.1016/S0022-2143(98)90039-7
Bright, 1831
Brin, 1987, Localized injections of botulinum toxin for the treatment of focal dystonia and hemifacial spasm, Mov Disord, 2, 237, 10.1002/mds.870020402
Brissaud, 1895
Broadbent, 1869, On the pathology of chorea, Br Med J, 86, 345, 10.1136/bmj.1.433.345
Browning, 1908, Rev. Charles Oscar Waters, M.D, Neurographs, 1, 137
Browning, 1908, Irving Whitall Lyon, M.D, Neurographs, 1, 147
Brusa, 2004, Progressive supranuclear palsy: new disease or variant of postencephalitic parkinsonism, Mov Disord, 19, 247, 10.1002/mds.10699
Bull, 1993, The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene, Nat Genet, 5, 327, 10.1038/ng1293-327
Burke, 1986, Torsion dystonia: a double-blind, prospective trial of high-dosage trihexphenidyl, Neurology, 36, 160, 10.1212/WNL.36.2.160
Burns, 1983, A primate model of parkinsonism: selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, Proc Natl Acad Sci USA, 80, 4546, 10.1073/pnas.80.14.4546
Burr, 1895, Local spasms. Occupation spasms, 275
Butler, 1979, Biogenic amine metabolism in Tourette syndrome, Ann Neurol, 6, 37, 10.1002/ana.410060109
Buzzard, 1872, Two cases of impaired writing power treated successfully by electricity, Practitioner, 9, 65
Calne, 1971, Idiopathic parkinsonism treated with extracerebral decarboxylase inhibitor in combination with levodopa, Br Med J, 3, 729, 10.1136/bmj.3.5777.729
Calne, 1974, Bromocriptine in parkinsonism, Br Med J, 4, 442, 10.1136/bmj.4.5942.442
Campion, 1995, The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease, Genomics, 26, 254, 10.1016/0888-7543(95)80208-4
Canfield, 1884, A case of acute hemiplegic chorea; with autopsy and remarks, Boston Medical and Surgical Journal, 111, 220, 10.1056/NEJM188409041111002
Carlsson, 1959, The occurrence, distribution and physiological role of catecholamines in the nervous system, Pharmacol Rev, 11, 490
Carlsson, 2003, A half-century of neurotransmitter research: impact on neurology and psychiatry, 303
Carlsson, 1957, 3,4-dihydroxyphenylalanine and 5-hydroxytryptophan as reserpine antagonists, Nature, 180, 1200, 10.1038/1801200a0
Carpenter, 1950, Athetosis and the basal ganglia: Review of the literature and study of forty-two cases, Arch Neurol Psychiatry, 63, 875, 10.1001/archneurpsyc.1950.02310240034002
Carpenter, 1955, Ballism associated with partial destruction of the subthalamic nucleus of Luys, Neurology, 5, 479, 10.1212/WNL.5.7.479
Carpenter, 1951, Analysis of somatotopic relations of the corpus Luysi in man and monkey: relation between the site of dyskinesia and distribution of lesions within the subthalamic nucleus, J Comp Neurol, 95, 349, 10.1002/cne.900950205
Carpenter, 1950, Analysis of choreoid hyperkinesias in the rhesus monkey. Surgical and pharmacological analysis of hyperkinesias resulting from lesions in the subthalamic nucleus of Luys, J Comp Neurol, 92, 293, 10.1002/cne.900920303
Charcot, 1877, On paralysis agitans, 129
Charcot, 1881, On athetosis, Vol. 2, 390
Charcot, 1887, Tremblements et mouvements chroréiformes. Chorée rhythmée, 209
Charcot, 1887, Gilles de la Tourette syndrome: a child with convulsive tic and coprolalia: December 13, 1887, 56
Charcot, 1889, Tremors and choreiform movements – rhythmical chorea, Vol. 3, 183
Charcot, 1861, De la paralysie agitante, Gazette Hebdomadaire de Médecine et de Chirurgie, 8, 765
Chen, 1995, The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysis, Genomics, 26, 425, 10.1016/0888-7543(95)80237-G
Chien, 1967, Drug-induced extra-pyramidal symptoms and their relations to clinical efficacy, Am J Psychiatry, 123, 1490, 10.1176/ajp.123.12.1490
Ciechanover, 2005, Intracellular protein degradation: from a vague idea through the lysosome and the ubiquitin-proteasome system and onto human diseases and drug targeting, 151
Coburn, 1931
Coburn, 1939, The prophylactic use of sulfonamide in streptococcal respiratory infections, with special reference to rheumatic fever, J Clin Invest, 18, 147, 10.1172/JCI101016
Cohen, 1979, Central biogenic amine metabolism in children with syndrome of chronic multiple tics of Gilles de la Tourette: norepinephrine, serotonin, and dopamine, J Am Acad Child Psychiatry, 18, 320, 10.1016/S0002-7138(09)61046-3
Conn, 1960, Asterixis in non-hepatic disorders, Am J Med, 29, 647, 10.1016/0002-9343(60)90098-X
Corbin, 1949, Trihexyphenyl: evaluation of a new agent in the treatment of Parkinson's disease, JAMA, 141, 373, 10.1001/jama.1949.02910060015004
Correns, 1900, Mendel's Regel über das Verhalten der Nachkommenschaft der Rassenbastarde, Berichte der Deutschen Botanischen Gesellschaft, 18, 158, 10.1111/j.1438-8677.1900.tb04893.x
Corrodi, 1973, Effect of ergot drugs on central catecholamine neurons: evidence for a stimulation of central dopamine neurons, J Pharm Pharmacol, 25, 409, 10.1111/j.2042-7158.1973.tb10037.x
Cotzias, 1967, Aromatic acids and modification of parkinsonism, N Engl J Med, 276, 374, 10.1056/NEJM196702162760703
Cotzias, 1969, Modification of parkinsonism – chronic treatment with L-dopa, N Engl J Med, 280, 337, 10.1056/NEJM196902132800701
Cotzias, 1970, Similarities between neurologic effects of DOPA and of apomorphine, N Engl J Med, 282, 31, 10.1056/NEJM197001012820107
Cotzias, 1976, Treatment of Parkinson disease with apomorphines: possible role of growth hormone, N Engl J Med, 294, 567, 10.1056/NEJM197603112941101
Coyle, 1976, Lesion of striatal neurons with kainic acid provides a model for Huntington's chorea, Nature, 263, 244, 10.1038/263244a0
Creutzfeldt, 1920, Über eine eigenartige herdomige Erkrankung des Zentralnervensystems, Z Gesamte Neurol Psychiatr, 57, 1, 10.1007/BF02866081
Critchley, 1949, Observations on essential (heredofamilial) tremor, Brain, 72, 113, 10.1093/brain/72.2.113
Crossman, 1989, Neural mechanism in disorders of movement, Comp Biochem Physiol A, 93, 141, 10.1016/0300-9629(89)90201-6
Cumings, 1948, The copper and iron content of brain and liver in the normal and in hepatolenticular degeneration, Brain, 71, 410, 10.1093/brain/71.4.410
Cumings, 1951, The effects of BAL in hepatolenticular degeneration, Brain, 74, 10, 10.1093/brain/74.1.10
Dale, 2004, Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity, Brain, 127, 21, 10.1093/brain/awh008
Dana, 1887, Hereditary tremor: a hitherto undescribed form of motor neurosis, Am J Med Sci, 94, 386, 10.1097/00000441-188710000-00005
Davies, 1997, Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation, Cell, 90, 537, 10.1016/S0092-8674(00)80513-9
Davis, 1951, Benign essential (heredofamilial) tremor, Arch Intern Med, 87, 808, 10.1001/archinte.1951.03810060035004
Davis, 1979, Chronic parkinsonism secondary to intravenous injections of meperidine analogues, Psychiatry Res, 1, 249, 10.1016/0165-1781(79)90006-4
Dawbarn, 1985, Survival of basal ganglia neuropeptide Y-somatostatin neurons in Huntington's disease, Brain Res, 340, 251, 10.1016/0006-8993(85)90921-7
Dawson, 1934, Cellular inclusions in cerebral lesions of epidemic encephalitis (Second report), Arch Neurol Psychiatry, 31, 685, 10.1001/archneurpsyc.1934.02250040009001
de la Boë, 1663
De Vries, 1900, Sur la loi de disjonction des hybrides, C R Acad Sci, 130, 845
Degwitz, 1960, Über die Wirkungen des L-DOPA beim Menschen und deren Beeinflussung durch Reserpin, Chlorpromazin, Iproniazid und Vitamin B6, Wien Klin Wochenschr, 38, 120, 10.1007/BF02189076
Dejerine, 1900, 13, 330
Dejerine, 1900, Olivopontocerebellar atrophy, 219
Delay, 1952, Utilisation en thérapeutique psychiatrique d'une phénothiazine d'action centrale élective, Ann Med Psychol (Paris), 110, 112
DeLong, 1990, Primate models of movement disorders of basal ganglia origin, Trends Neurosci, 13, 281, 10.1016/0166-2236(90)90110-V
Dening, 1990, Eponymous confusion over Bruno Fleischer, Lancet, 335, 291, 10.1016/0140-6736(90)90108-H
Denny Brown, 1951, The effects of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease), N Engl J Med, 245, 917, 10.1056/NEJM195112132452401
Dewey, 1989, Hemiballism-hemichorea. Clinical and pharmacologic findings in 21 patients, Arch Neurol, 46, 862, 10.1001/archneur.1989.00520440044020
Dickman, 2001, Von Economo encephalitis, Arch Neurol, 58, 1696, 10.1001/archneur.58.10.1696
DiFiglia, 1997, Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain, Science, 277, 1990, 10.1126/science.277.5334.1990
Dooling, 1975, The pathological anatomy of posthemiplegic athetosis, Brain, 98, 29, 10.1093/brain/98.1.29
Dorshay, 1949, Active therapy for parkinsonism, JAMA, 140, 1317
Dupont, 1973, Treatment of benign essential tremor with propranolol. A controlled clinical trial, Acta Neurol Scand, 49, 75, 10.1111/j.1600-0404.1973.tb01280.x
Duyao, 1993, Trinucleotide repeat length instability and age of onset in Huntington's disease, Nat Genet, 4, 387, 10.1038/ng0893-387
Ehringer, 1960, Verteilung von Adrenalin und Dopamin (3-Hydroxytyramin) im Gehim des Menschen und ihr Verhalten bei Erkrankungen des extrapyramidalen Systems, Wien Klin Wochenschr, 38, 1236, 10.1007/BF01485901
Eldridge, 1970, The torsion dystonias: literature review and genetic and clinical studies, Neurology, 20, 1, 10.1212/WNL.20.11_Part_2.1
Elston, 1985, Effect of treatment with botulinum toxin on neurogenic blepharospasm, Br Med J (Clin Res Ed), 290, 1857, 10.1136/bmj.290.6485.1857
Ernst, 1965, Relation between action of dopamine and apomorphine and the O-methylated derivatives upon the CNS, Psychopharmacology (Berl), 7, 391, 10.1007/BF00402361
Eschner, 1897, A graphic study of tremor, J Exp Med, 2, 301, 10.1084/jem.2.3.301
Fahn, 1983, High-dosage anticholinergic therapy in dystonia, Adv Neurol, 37, 177
Fahn, 1988, Concept and classification of dystonia, Adv Neurol, 50, 1, 10.1212/WNL.50.5_Suppl_5.S1
Farrer, 1992, Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting, Am J Hum Genet, 50, 528
Faurbye, 1964, Neurological symptoms in pharmacotherapy of psychosis, Acta Psychiatr Scand, 40, 10, 10.1111/j.1600-0447.1964.tb05731.x
Fehling, 1966, Treatment of Parkinson's syndrome with L-DOPA: a double blind study, Acta Neurol Scand, 42, 367, 10.1111/j.1600-0404.1966.tb01188.x
Ferrante, 1985, Selective sparing of a class of striatal neurons in Huntington's disease, Science, 230, 561, 10.1126/science.2931802
Ferrante, 1987, Morphologic and histochemical characteristics of a spared subset of striatal neurons in Huntington's disease, J Neuropathol Exp Neurol, 46, 12, 10.1097/00005072-198701000-00002
Ferrier, 1876
Findley, 1985, Primidone in essential tremor of the hands and head: a double-blind controlled clinical study, J Neurol Neurosurg Psychiatry, 481, 911, 10.1136/jnnp.48.9.911
Flatau, 1911, Progressiver Torsionspasmus bei Kindern, Z Gesamte Neurol Psychiatr, 7, 586, 10.1007/BF02865155
Fleischer, 1903, Zwei weitere Fälle von grünlicher Verfärbung der Kornea, Klin Monatsbl Augenheilkd, 41, 335
Foley, 2000, The L-DOPA story revisited. Further surprises to be expected? The contribution of Isamu Sano to the investigation of Parkinson's disease, J Neural Transm Suppl, 60, 1
Foley, 2003, Beans, roots and leaves: a brief history of the pharmacological therapy of parkinsonism, Wurzbg Medizinhist Mitt, 22, 215
Forel, 1877, Untersuchungen über die Haubenregion und ihre oberen Verknupfungen im Gehirne des Menschen und einiger Saügethiere, mit Beiträgen zu den Methoden des Gehirnuntersuchungen, Arch Psychiatr Nervenkr, 7, 182, 10.1007/BF02041873
Forno, 1986, Locus ceruleus lesions and eosinophilic inclusions in MPTP-treated monkeys, Ann Neurol, 20, 449, 10.1002/ana.410200403
Freyhan, 1957, Psychomotility and parkinsonism in treatment with neuroleptic drugs, Arch Neurol Psychiatry, 78, 465, 10.1001/archneurpsyc.1957.02330410029003
Friedreich, 1863, Über degenerative Atrophie der spinalen Hinterstränge, Virchows Arch Pathol Anat Physiol Klin Med 26: 391–419, 433–459;, 27, 1, 10.1007/BF01938516
Friedreich, 1881, Neuropathologische Beobachtung beim Paramyoklonus Multiplex, Virchows Arch Pathol Anat Physiol Klin Med, 86, 421, 10.1007/BF01915725
Fritsch, 1870, On the electrical excitability of the cerebrum, 73
Frucht, 2000, The clinical spectrum of posthypoxic myoclonus, Mov Disord, 15, 2, 10.1002/mds.870150702
Frydman, 1985, Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus, Proc Natl Acad Sci USA, 82, 1819, 10.1073/pnas.82.6.1819
Furtado, 1996, Relationship between trinucleotide repeats and neuropathological changes in Huntington's disease, Ann Neurol, 39, 132, 10.1002/ana.410390120
Galilei, 1610, Letter dated January 7, 1610, 147
Giasson, 2000, Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions, Science, 290, 985, 10.1126/science.290.5493.985
Gibb, 1989, Corticobasal degeneration, Brain, 112, 1171, 10.1093/brain/112.5.1171
Gildenberg, 1998, The history of surgery for movement disorders, Neurosurg Clin N Am, 9, 283, 10.1016/S1042-3680(18)30264-X
Gilles de la Tourette, 1881, Les “sauteurs” du Maine (États-Unis): Par G, Beard. Arch Neurol (Paris), 2, 146
Gilles de la Tourette, 1884, Jumping, Latah, Myriachit, Arch Neurol (Paris), 8, 68
Gilles de la Tourette, 1885, Étude sur une affection nerveuse caracterisée par l'incoordination motrice accompagnée d'écholalie et de coprolalie, Arch Neurol (Paris), 9, 19
Gilliam, 1987, Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere, Cell, 50, 565, 10.1016/0092-8674(87)90029-8
Gilman, 1997, G proteins and regulation of adenylyl cyclase, 182
Glazebrook, 1945, Wilson's disease, Edinburgh Med J, 52, 83
Goetz, 1986, Charcot on Parkinson's disease, Mov Disord, 1, 27, 10.1002/mds.870010104
Goetz, 1982, Gilles de la Tourette on Tourette syndrome, Adv Neurol, 35, 1
Goetz, 1995, 113
Goetz, 2001, The basal ganglia: part 1 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 152, 10.1002/1531-8257(200101)16:1<152::AID-MDS1027>3.0.CO;2-I
Goetz, 2001, The history of Parkinson's disease: part 2 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 156, 10.1002/1531-8257(200101)16:1<156::AID-MDS1028>3.0.CO;2-B
Goetz, 2001, Seminal figures in the history of movement disorders: Sydenham, Parkinson, and Charcot: part 6 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 537, 10.1002/mds.1113
Goetz, 2001, Parkinson-plus syndromes: part 7 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 541, 10.1002/mds.1114
Goetz, 2001, History of chorea: part 3 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 331, 10.1002/mds.1066
Goetz, 2001, Seminal figures in the history of movement disorders: Gilles de la Tourette, Oppenheim, the Vogts, von Economo, Wilson, and Marsden: part 12 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 940, 10.1002/mds.1189
Goetz, 2001, History of dystonia: part 4 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 339, 10.1002/mds.1067
Goetz, 2001, History of myoclonus: part 8 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 545, 10.1002/mds.1115
Goetz, 2001, History of tic disorders and Gilles de la Tourette syndrome: part 5 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 346, 10.1002/mds.1068
Goff, 1991, The effect of benztropine on haloperidol-induced dystonia, clinical efficacy and pharmacokinetics: a prospective, double-blind trial, J Clin Psychopharmacol, 11, 106
Golbe, 1990, A large kindred with autosomal dominant Parkinson's disease, Ann Neurol, 27, 276, 10.1002/ana.410270309
Goldman, 1992, The symptomatic and functional outcome of stereotactic thalamotomy for medically intractable essential tremor, J Neurosurg, 76, 924, 10.3171/jns.1992.76.6.0924
Goldstein, 1966, The effects of ventromedial segmental lesions on the biosynthesis of catecholamines in the striatum, Life Sci, 5, 2171, 10.1016/0024-3205(66)90078-6
Gowers, 1876, On “athetosis” and post-hemiplegic disorders of movement, Med Chir Trans, 271, 10.1177/095952877605900119
Gowers, 1888
Gowers, 1906, On tetanoid chorea and its association with cirrhosis of the liver, Reviews of Neurology and Psychiatry, 4, 249
Graham, 1969, Orthostatic hypotension, and nicotine sensitivity in a case of multiple system atrophy, J Neurol Neurosurg Psychiatry, 32, 28, 10.1136/jnnp.32.1.28
Greenfield, 1953, The brain-stem lesions in parkinsonism, J Neurol Neurosurg Psychiatry, 16, 213, 10.1136/jnnp.16.4.213
Greenfield, 1922, The pathology of Sydenham's chorea, Lancet, 2, 603, 10.1016/S0140-6736(01)01044-3
Groth, 1973, Hepatic transplantation in Wilson disease, Birth Defects Orig Artic Ser, 9, 106
Grundmann, 2005, Primary torsion dystonia, Arch Neurol, 62, 682, 10.1001/archneur.62.4.682
Guridi, 2001, The subthalamic nucleus, hemiballismus and Parkinson's disease: reappraisal of a neurosurgical dogma, Brain, 124, 5, 10.1093/brain/124.1.5
Gusella, 1983, A polymorphic DNA marker genetically linked to Huntington's disease, Nature, 306, 234, 10.1038/306234a0
Gusella, 1985, Deletion of Huntington's disease linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome, Nature, 318, 75, 10.1038/318075a0
Hall, 1921, La Dégénérescence Hepatolenticulare
Hall, 1956, Neurotoxic reactions resulting from chlorpromazine administration, JAMA, 161, 214, 10.1001/jama.1956.02970030032008
Hallett, 1986, Early history of myoclonus, Adv Neurol, 43, 7
Hamada, 1992, Excitotoxic acid lesions of the primate subthalamic nucleus result in reduced pallidal neuronal activity during active holding, J Neurophysiol, 68, 1859, 10.1152/jn.1992.68.5.1859
Hamani, 2003, The subthalamic nucleus in the context of movement disorders, Brain, 127, 4, 10.1093/brain/awh029
Haméleers, 2006, History of the corpus Luysii: 1865–1995, Arch Neurol, 63, 1340, 10.1001/archneur.63.9.1340
Hammond, 1890, Pathological findings in the original case of athetosis, J Nerv Ment Dis, 17, 555
Hammond, 1871, Athetosis, 654
Hammond, 1884, Miryachit: a newly described disease of the nervous system, and its analogues, New York Medical Journal, 39, 191
Hammond, 1893, Athetosis, 315
Hamon, 1952, Remarques sur l'action du 4560 RP sur l'agitation maniaque, Ann Med Psychol (Paris), 110, 331
Haškovec, 1901, L'Akathisie, Rev Neurol, 9, 1107
Hassler, 1938, Zur Pathologie der Paralysis agitans und des post-encephalitischen Parkinsonismus, Journal für Psychologie und Neurologie, 18, 387
Hassler, 1954, Indikationen und Lokalisationsmethode der gezielten Hirnoperationen, Nervenartz, 25, 441
Haurowitz, 1930, Über eine Anomalie des Kupferstoffwechsels, Hoppe-Seylers Z Physiol Chem, 190, 72, 10.1515/bchm2.1930.190.1-2.72
Hayashi, 2000, An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene, Mov Disord, 15, 884, 10.1002/1531-8257(200009)15:5<884::AID-MDS1019>3.0.CO;2-8
Heikkila, 1984, Protection against the dopaminergic neurotoxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine by monoamine oxidase inhibitors, Nature, 311, 467, 10.1038/311467a0
Hershko, 2005, The ubiquitin system for protein degradation and some of its roles in the control of the cell division cycle, 187
Herz, 1944, Dystonia I. Historical review, analysis of dystonic symptoms and psychologic mechanisms involved, Arch Neurol Psychiatry, 51, 305, 10.1001/archneurpsyc.1944.02290280003001
Herz, 1944, Dystonia II. Clinical classification, Arch Neurol Psychiatry, 51, 319, 10.1001/archneurpsyc.1944.02290280017002
Herz, 1944, Dystonia III. Pathology and conclusions, Arch Neurol Psychiatry, 52, 20, 10.1001/archneurpsyc.1944.02290310026002
Holdorff, 2002, Friedrich Heinrich Lewy (1885–1950) and his work, J Hist Neurosci, 11, 19, 10.1076/jhin.11.1.19.9106
Holmberg, 1947, Investigations in serum copper. I. Nature of serum copper and its relation to the iron-binding protein in human serum, Acta Chem Scand, 1, 944, 10.3891/acta.chem.scand.01-0944
Holmberg, 1948, Investigations in serum copper. II. Isolation of the copper containing protein, and a description of some of its properties, Acta Chem Scand, 2, 550, 10.3891/acta.chem.scand.02-0550
Hoogenraad, 1979, Oral zinc sulfate as long-term treatment in Wilson's disease (hepatolenticular degeneration), Eur Neurol, 18, 205, 10.1159/000115077
Hoogenraad, 1987, Management of Wilson's disease with zinc sulfate: experience in a series of 27 patients, J Neurol Sci, 77, 137, 10.1016/0022-510X(87)90116-X
Hoogeveen, 1993, Characterization and localization of the Huntington disease gene product, Hum Molec Genet, 2, 2069, 10.1093/hmg/2.12.2069
Hornykiewicz, 2001, How L-DOPA was discovered as a drug for Parkinson's disease 40 years ago, Wien Klin Wochenschr, 113, 855
Howard, 1992, From the jumping Frenchmen of Maine to post-traumatic stress disorder: the startle response in neuropsychiatry, Psychol Med, 22, 695, 10.1017/S0033291700038137
Huntington, 1872, On chorea, Medical and Surgical Reporter, 26, 317
1993, A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes, Cell, 72, 971, 10.1016/0092-8674(93)90585-E
Husby, 1976, Antibodies reacting with cytoplasm of subthalamic and caudate nuclei neurons in chorea and acute rheumatic fever, J Exp Med, 144, 1094, 10.1084/jem.144.4.1094
Ishikawa, 1995, A family with hereditary juvenile dystonia-parkinsonism, Mov Disord, 10, 482, 10.1002/mds.870100413
Itard, 1825, Mémoire sur quelques fonctions involontaires des appareils de la locomotion, de la préhension et de la voix, Archives Générales de Medecine, 8, 385
Jackson, 1868, Observations on the physiology and pathology of hemi-chorea, Vol. 2, 238
Jackson, 1876, On epilepsies and on the after-effects of epileptic discharges (Todd and Robertson's hypothesis), 135
Jager, 1955, Hereditary tremor, Arch Intern Med, 95, 788, 10.1001/archinte.1955.00250120024003
Jakes, 1994, Identification of two distinct synucleins from human brain, FEBS Lett, 345, 27, 10.1016/0014-5793(94)00395-5
Jakob, 1921, Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswerten anatomischen Befunden (spastische Pseudosklerose, Encephalomyelopathie mit disseminierten Degenerationsherden), Z Gesamte Neurol Psychiatr, 64, 147, 10.1007/BF02870932
Jankovic, 1995, Outcomes after stereotactic thalamotomy for parkinsonian, essential, and other types of tremor, Neurosurgery, 37, 680, 10.1227/00006123-199510000-00011
Johnson, 1990, Twin studies and the genetics of Parkinson's disease – a reappraisal, Mov Disord, 5, 187, 10.1002/mds.870050302
Jummani, 2001, Sydenham chorea, Arch Neurol, 58, 311, 10.1001/archneur.58.2.311
Kann, 2002, Role of parkin mutations in 111 community-based patients with early-onset parkinsonism, Ann Neurol, 51, 621, 10.1002/ana.10179
Kayser, 1902, Über einen Fall von angeborener grünlicher Verfärbung der Cornea, Klin Monstbl Augenheilkd, 40, 22
Kebabian, 1979, Multiple receptor mechanism for dopamine, Nature, 227, 93, 10.1038/277093a0
Keppel Hesselink, 1996, Evolution of concepts and definitions of Parkinson's disease since 1817, J Hist Neurosci, 5, 200, 10.1080/09647049609525668
Kitada, 1998, Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism, Nature, 392, 605, 10.1038/33416
Klawans, 1976, Treatment and prognosis of hemiballismus, N Engl J Med, 295, 1348, 10.1056/NEJM197612092952404
Klawans, 1978, Gilles de la Tourette syndrome after long-term chlorpromazine therapy, Neurology, 28, 1064, 10.1212/WNL.28.10.1064
Klempel, 1974, Gilles de la Tourette's symptoms induced by L-dopa, S Afr Med J, 48, 1379
Koehler, 1997, Tremor in Latin texts of Dutch physicians: 16th–18th centuries, Mov Disord, 12, 798, 10.1002/mds.870120531
Kopp, 1836
Krack, 1999, Relics of dancing mania: the dancing procession of Echternach, Neurology, 53, 2169, 10.1212/WNL.53.9.2169
Krack, 2003, Five-year follow-up of bilateral stimulation of the subthalamic nucleus in advanced Parkinson's disease, N Engl J Med, 349, 1925, 10.1056/NEJMoa035275
Kristensen, 1985, Progressive supranuclear palsy – 20 years later, Acta Neurol Scand, 71, 177, 10.1111/j.1600-0404.1985.tb03186.x
Kruisdijk, 2007, Botulinum toxin for writer's cramp: a randomised, placebo-controlled trial and 1-year follow-up, J Neurol Neurosurg Psychiatry, 78, 264, 10.1136/jnnp.2005.083170
Kruse, 1960, Persistent muscular restlessness after phenothiazine treatment: report of three cases, Am J Psychiatry, 117, 152, 10.1176/ajp.117.2.152
Kunkle, 1965, The “jumpers” of Maine: past history and present status, J Maine Med Assoc, 56, 191
Kunkle, 1967, The “jumpers” of Maine: a reappraisal, Arch Intern Med, 119, 355, 10.1001/archinte.1967.00290220105005
Kurczynski, 1983, Hyperekplexia, Arch Neurol, 40, 246, 10.1001/archneur.1983.04050040076015
Kushner, 1999, A perplexing document in the early history of Gilles de la Tourette syndrome: Melotti's rendition of a “Lecture by Charcot” (including a complete translation from the Italian with commentary), J Hist Neurosci, 8, 5, 10.1076/jhin.8.1.5.1779
Lahti, 1995, D2-family receptor distribution in human postmortem tissue: an autoradiographic study, Neuroreport, 6, 2502, 10.1097/00001756-199512150-00015
Laitinen, 1992, Leksell's posteroventral pallidotomy in the treatment of Parkinson's disease, J Neurosurg, 76, 53, 10.3171/jns.1992.76.1.0053
Laitinen, 1992, Ventroposterolateral pallidotomy can abolish all parkinsonian symptoms, Stereotact Funct Neurosurg, 58, 14, 10.1159/000098965
Lajonchere, 1996, Gilles de la Tourette and the discovery of Tourette syndrome: includes a translation of his 1884 article, Arch Neurol, 53, 567, 10.1001/archneur.1996.00550060111024
Lance, 1963, The syndrome of intention or action myoclonus as a sequel to hypoxic encephalopathy, Brain, 86, 111, 10.1093/brain/86.1.111
Lance, 2001, Negative myoclonus in posthypoxic patients: historical note, Mov Disord, 16, 162, 10.1002/1531-8257(200101)16:1<162::AID-MDS1029>3.0.CO;2-9
Lang, 1982, Anticholinergics in adult-onset focal dystonia, Can J Neurol Sci, 9, 313, 10.1017/S0317167100044139
Langston, 1995
Langston, 1983, Chronic parkinsonism in humans due to a product of meperidine-analog synthesis, Science, 219, 979, 10.1126/science.6823561
Langston, 1984, Pargyline prevents MPTP-induced parkinsonism in primates, Science, 225, 1480, 10.1126/science.6332378
Lanska, 2000, 19th-century American contributions to the recording of tremors, Mov Disord, 15, 720, 10.1002/1531-8257(200007)15:4<720::AID-MDS1019>3.0.CO;2-1
Lanska, 2000, George Huntington (1850–1916) and hereditary chorea, J Hist Neurosci, 9, 76, 10.1076/0964-704X(200004)9:1;1-2;FT076
Lanska, 2001, Characteristics and lasting contributions of 19th-century American neurologists, J Hist Neurosci, 10, 202, 10.1076/jhin.10.2.202.7252
Lanska, 2002, Classic articles by 19th-century American neurologists: a critical review, J Hist Neurosci, 11, 156, 10.1076/jhin.11.2.156.15196
Lanska, 2002, Limb immobilization for the treatment of focal occupational dystonia [Letter], Neurology, 58, 991, 10.1212/WNL.58.6.991
Lanska, 2002, 19th-century instruments for writer's cramp [Abstract], Neurology, 58, A341
Lanska, 2001, Development of instruments for abnormal movements: dynamometers, the dynamograph, and tremor recorders: part 9 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 736, 10.1002/mds.1155
Lanska, 2001, Seminal figures in the history of movement disorders: Huntington, Osler, and Hammond: part 11 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, Spain, June 2000, Mov Disord, 16, 749, 10.1002/mds.1157
Lantos, 1998, The definition of multiple system atrophy: a review of recent developments, J Neuropathol Exp Neurol, 57, 1099, 10.1097/00005072-199812000-00001
Larsson, 1960, Essential tremor: a clinical and genetic population study, Acta Psychiatr Scand, 26, 1
Leavitt, 1964, Studies in asterixis. Part I, Arch Neurol, 10, 360, 10.1001/archneur.1964.00460160030002
Leeflang, 1999, Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism, Hum Mol Genet, 8, 173, 10.1093/hmg/8.2.173
Lehmann, 1954, Chlorpromazine: new inhibiting agent for psychomotor excitement and manic states, AMA Arch Neurol Psychiatry, 71, 227, 10.1001/archneurpsyc.1954.02320380093011
Lewis, 1885, The neural disorders of writers and artisans, 504
Lewy, 1913, Zur pathologischen Anatomie der Paralysis agitans, Dtsch Z Nervenheilkd, 50, 50
Limousin, 1995, Effect of parkinsonian signs and symptoms of bilateral subthalamic nucleus stimulation, Lancet, 345, 91, 10.1016/S0140-6736(95)90062-4
Limousin, 1998, Electrical stimulation of the subthalamic nucleus in advanced Parkinson's disease, N Engl J Med, 339, 1105, 10.1056/NEJM199810153391603
Limousin, 1999, Multicentre European study of thalamic stimulation in parkinsonian and essential tremor, J Neurol Neurosurg Psychiatry, 66, 289, 10.1136/jnnp.66.3.289
Lindemulder, 1933, Familial myoclonia occurring in three successive generations, J Nerv Ment Dis, 77, 489, 10.1097/00005053-193305000-00003
Lloyd, 1975, The neurochemistry of Parkinson's disease: effect of L-dopa therapy, J Pharmacol Exp Ther, 195, 453
Louis, 1997, The shaking palsy, the first forty-five years: a journey through the British literature, Mov Disord, 12, 1068, 10.1002/mds.870120638
Louis, 2001, Etiology of essential tremor: should we be searching for environmental causes, Mov Disord, 16, 822, 10.1002/mds.1183
Lucking, 2000, Association between early-onset Parkinson's disease and mutations in the parkin gene, N Engl J Med, 342, 1560, 10.1056/NEJM200005253422103
Lundborg, 1903
Luys, 1865
Lyon, 1863, Chronic hereditary chorea, American Medical Times, 7, 289
Ma, 2006, Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes, Mov Disord, 21, 1368, 10.1002/mds.20950
McCall, 2001, Influenza RNA not detected in archival brain tissues from acute encephalitis lethargica cases or in postencephalitic Parkinson cases, J Neuropathol Exp Neurol, 60, 696, 10.1093/jnen/60.7.696
McGeer, 1976, Duplication of biochemical changes of Huntington's chorea by intrastriatal injections of glutamic acid and kainic acids, Nature, 263, 517, 10.1038/263517a0
McGeer, 1964, Administration of dihydroxyphenylalanine to parkinsonian patients, Can Med Assoc J, 90, 463
Markey, 1984, Intraneuronal generation of a pyrimidium ion metabolite may cause drug-induced parkinsonism, Nature, 311, 464, 10.1038/311464a0
Marsden, 1985, The anatomical basis of symptomatic hemidystonia, Brain, 108, 463, 10.1093/brain/108.2.463
Martin, 1927, Hemichorea resulting from a local lesion of the brain: the syndrome of the body of Luys, Brain, 50, 637, 10.1093/brain/50.3-4.637
Martin, 1957, Hemichorea (hemiballismus) without lesions in the corpus Luysii, Brain, 80, 1, 10.1093/brain/80.1.1
Matsumine, 1997, Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27, Am J Hum Genet, 60, 588
Mauriello, 1985, Blepharospasm, Meige syndrome, and hemifacial spasm: treatment with botulinum toxin, Neurology, 35, 1499, 10.1212/WNL.35.10.1499
Meige, 1907, 27
Mendel, 1865, Versuche über Pflanzenhybriden, Verhandlungen des Naturfarschenden Vereines in Brünn, 4, 3
Merritt, 1969, Juvenile Huntington's chorea, 645
Meyers, 1940, Surgical procedure for postencephalitic tremor, with notes on the physiology of premotor fibers, Arch Neurol Psychiatry, 44, 455
Mink, 2003, The basal ganglia and involuntary movements: impaired inhibition of competing motor patterns, Arch Neurol, 60, 1365, 10.1001/archneur.60.10.1365
Mitchell, 1980, Gilles de la Tourette's disease associated with pemoline, Am J Psychiatry, 137, 1617
Mitchell, 1985, Sites of the neurotoxic action of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in the monkey include the ventral tegmental area and the locus coeruleus, Neurosci Lett, 61, 195, 10.1016/0304-3940(85)90424-0
Mitchell, 1903, Report of a case of familial tremor of the head, J Nerv Ment Dis, 30, 158, 10.1097/00005053-190303000-00003
Mitchell, 1874, Post-paralytic chorea, Am J Med Sci, 68, 342, 10.1097/00000441-187410000-00002
Molina-Negro, 1975, Semiology of tremors, Can J Neurol Sci, 2, 23, 10.1017/S0317167100019946
Montagu, 1957, Catechol compounds in rat tissues and in brains of different animals, Nature, 180, 245, 10.1038/180244a0
Myers, 1982, Factors related to onset age of Huntington disease, Am J Hum Genet, 34, 481
Narbona, 1984, Hemidystonia secondary to localized basal ganglia tumour, J Neurol Neurosurg Psychiatry, 47, 704, 10.1136/jnnp.47.7.704
Nausieda, 1980, Sydenham chorea: an update, Neurology, 30, 331, 10.1212/WNL.30.3.331
Nutt, 1984, Cranial dystonia: double-blind crossover study of anticholinergics, Neurology, 34, 215, 10.1212/WNL.34.2.215
Obeso, 2000, Pathophysiology of levodopa-induced dyskinesias in Parkinson's disease: problems with the current model, Ann Neurol, 47, S22
O'Brien, 1981, Benign familial tremor treated with primidone, Br Med J, 282, 178, 10.1136/bmj.282.6259.178
Olney, 1978, Glutamic neurotoxicity and Huntington's chorea, Nature, 271, 557, 10.1038/271557a0
Olszewski, 1964, Pathological report on six cases of heterogeneous system degeneration, J Neuropathol Exp Neurol, 23, 187
Oppenheim, 1911, Über eine eigenartige Krampfkrankheit des kindlichen und jegendlichen Alters (Dysbasia lordotica progressiva, Dystonia musculorum deformans), Neurologisches Zentralblatt, 30, 1090
Ørbeck, 1959, An early description of Huntington's chorea, Med Hist, 3, 165, 10.1017/S0025727300024492
Osler, 1887, On the general etiology and symptoms of chorea: based on the records of 410 cases at the Infirmary for Nervous Diseases, Philadelphia, Medical News, 51, 437
Osler, 1894
Osler, 1908, Historical notes on hereditary chorea, Neurographs, 1, 113
Ozelius, 1989, Human gene for torsion dystonia located on chromosome 9q32-q34, Neuron, 2, 1427, 10.1016/0896-6273(89)90188-8
Ozelius, 1997, Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium, Genome Res, 7, 483, 10.1101/gr.7.5.483
Ozelius, 1997, The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein, Nat Genet, 17, 40, 10.1038/ng0997-40
Pahwa, 1999, Bilateral thalamic stimulation for the treatment of essential tremor, Neurology, 53, 1447, 10.1212/WNL.53.7.1447
Papp, 1992, Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophy, J Neurol Sci, 107, 172, 10.1016/0022-510X(92)90286-T
Papp, 1989, Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy–Drager syndrome), J Neurol Sci, 94, 79, 10.1016/0022-510X(89)90219-0
Parent, 2002, Jules Bernard Luys and the subthalamic nucleus, Mov Disord, 17, 181, 10.1002/mds.1251
Parkinson, 1817
Penny, 1997, CAG repeat number governs the development rate of pathology in Huntington's disease, Ann Neurol, 41, 689, 10.1002/ana.410410521
Perutz, 1994, Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases, Proc Natl Acad Sci USA, 91, 5355, 10.1073/pnas.91.12.5355
Petrukhin, 1993, Mapping, cloning and genetic characterization of the region containing the Wilson disease gene, Nat Genet, 5, 338, 10.1038/ng1293-338
Pettigrew, 1985, Hemidystonia: a report of 22 patients and a review of the literature, J Neurol Neurosurg Psychiatry, 48, 650, 10.1136/jnnp.48.7.650
Piccolomini, 1630
Poirer, 1965, Influence of the substantia nigra on the catecholamine content of the striatum, Brain, 88, 181, 10.1093/brain/88.1.181
Polymeropoulos, 1996, Mapping of a gene for Parkinson's disease to chromosome 4q21-q23, Science, 274, 1197, 10.1126/science.274.5290.1197
Polymeropoulos, 1997, Mutation in the alpha-synuclein gene identified in families with Parkinson's disease, Science, 276, 2045, 10.1126/science.276.5321.2045
Poore, 1878, An analysis of 75 cases of writer's cramp and impaired writing power, Med Chir Trans, 61, 111, 10.1177/095952877806100111
Posey, 1904, Paralysis of upward movement of the eyes, Ann Ophthalmol, 13, 523
Poynton, 1913
Pramstaller, 2005, Lewy body Parkinson's disease in a large pedigree with 77 parkin mutation carriers, Ann Neurol, 58, 411, 10.1002/ana.20587
Putnam, 1879, A new adjuvant in the treatment of writer's palsy, Boston Medical and Surgical Journal, 101, 320, 10.1056/NEJM187908281010913
Rabinovitch, 1965, An exaggerated startle reflex resembling a kicking horse, Can Med Assoc J, 93, 130
Rammelkamp, 1952, Studies on the epidemiology of rheumatic fever in the armed services, 72
Ranen, 1995, Anticipation and instability of IT-15(CAG)n repeats in parent-offspring pairs with Huntington's disease, Am J Hum Genet, 57, 593
Rebeiz, 1967, Corticodentatonigral degeneration with neuronal achromasia: a progressive disorder of late adult life, Trans Am Neurol Assoc, 92, 23
Rebeiz, 1968, Corticodentatonigral degeneration with neuronal achromasia, Arch Neurol, 18, 20, 10.1001/archneur.1968.00470310034003
Reid, 2001, Experimenting on the past: the enigma of Von Economo's encephalitis lethargica, J Neuropathol Exp Neurol, 60, 663, 10.1093/jnen/60.7.663
Reik, 1988, Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea, J Med Genet, 25, 805, 10.1136/jmg.25.12.805
Reiner, 1988, Differential loss of striatal projection neurons in Huntington disease, Proc Natl Acad Sci USA, 85, 5733, 10.1073/pnas.85.15.5733
Richardson, 1963, Supranuclear ophthalmoplegia, pseudobulbar palsy, nuchal dystonia and dementia: a clinical report on eight cases of “heterogeneous system degeneration, Trans Am Neurol Assoc, 88, 25
Ridley, 1988, Anticipation in Huntington's disease is inherited through the male line but may originate in the female, J Med Genet, 25, 589, 10.1136/jmg.25.9.589
Ridley, 1991, Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting, J Med Genet, 28, 224, 10.1136/jmg.28.4.224
Riley, 1990, Cortical-basal ganglionic degeneration, Neurology, 40, 1203, 10.1212/WNL.40.8.1203
Ristic, 2002, Long-term prognosis of vascular hemiballismus, Stroke, 33, 2109, 10.1161/01.STR.0000022810.76115.C0
Robins, 1885, The treatment of writers' cramp, Proc Phil Co Med Soc, 7, 271
Robins, 1885, Writers' cramp” and its treatment, with the notes of several cases, Am J Med Sci, 89, 452, 10.1097/00000441-188504000-00012
Rodbell, 1997, Signal transduction: evolution of an idea, 220
Roger, 1866, Recherches cliniques sur la chorea, sur le rhumatisme et sur les maladies du Coeur chez les enfants, Archives Générales de Médecine, 2, 641
Rose, 2005, Ubiquitin at fox chase, 218
Rothfus, 1988, Improvement of cerebral CT abnormalities following liver transplantation in a patient with Wilson disease, J Comput Assist Tomogr, 12, 138, 10.1097/00004728-198801000-00027
Rubinsztein, 1996, Phenotypic characterization of individuals with 30–40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36–39 repeats, Am J Hum Genet, 59, 16
Rumpel, 1913, Über das Wesen und die Bedeutung der Leberveränderungen und der Pigmentierungen bei den damit verbunderen Fällen von Pseudosklerose, zugleich ein Beitrag zur Lehre der Pseudosklerose (Westphal-Strumpell), Dtsch Z Nervenheilkd, 49, 54, 10.1007/BF01760543
Saint-Hilaire, 1986, Jumping Frenchmen of Maine, Neurology, 36, 1269, 10.1212/WNL.36.9.1269
Sano, 1959, Distribution of catechol compounds in human brain, Biochim Biophys Acta, 32, 586, 10.1016/0006-3002(59)90652-3
Scheinberg, 1952, Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease), Science, 116, 484, 10.1126/science.116.3018.484
Scheinberg, 1960, Long-term management of hepatolenticular degeneration (Wilson's disease), Am J Med, 29, 316, 10.1016/0002-9343(60)90028-0
Scherer, 1933, Beiträge zur pathologischen Anatomie des Kleinhirns. III. Mitteilung: Genuine Kleinhirnatrophien, Z Gesamte Neurol Psychiatr, 145, 335, 10.1007/BF02865875
Scherer, 1933, Extrapyramidale Störungen bei der olivopontocerebellaren Atrophie. Ein Beitrag zum Problem des lokalen vorzeitigen Alterns, Z Gesamte Neurol Psychiatr, 145, 406, 10.1007/BF02865876
Schiller, 1967, The vicissitudes of the basal ganglia (further landmarks in cerebral nomenclature), Bull Hist Med, 41, 515
Schiller, 1986, Parkinsonian rigidity: the first hundred-and-one years 1817–1918, Hist Philos Life Sci, 8, 221
Schiller, 2000, Fritz Lewy and his bodies, J Hist Neurosci, 9, 148, 10.1076/0964-704X(200008)9:2;1-Y;FT148
Schonecker, 1957, Ein eigentumliches Syndrom im oralen Bereich bei Megaphen Applikation, Nervenarzt, 28, 35
Schouwink, 1961
Schuurman, 2000, A comparison of continuous thalamic stimulation and thalamotomy for suppression of severe tremor, N Engl J Med, 342, 461, 10.1056/NEJM200002173420703
Schwab, 1951, Apomorphine in Parkinson's disease, Trans Am Neurol Assoc, 76, 273
Schwalbe, 1908
Scott, 1973, Pharmacologic weakening of extraocular muscles, Invest Ophthalmol Vis Sci, 12, 924
Sée, 1850, De la choreé, Mémoires de l'Académie Royale de Médecine (Paris), 15, 374
Seignot, 1961, A case of the syndrome of tics of Gilles de la Tourette controlled by R 1625, Ann Med Psychol, 28, 92
Shahani, 1976, Physiological and pharmacological aids in the differential diagnosis of tremor, J Neurol Neurosurg Psychiatry, 39, 772, 10.1136/jnnp.39.8.772
Shahzadi, 1995, Thalamotomy for essential and cerebellar tremor, Stereotact Funct Neurosurg, 565, 11, 10.1159/000098890
Shapiro, 1973, Treatment of Tourette's syndrome: with haloperidol, review of 34 cases, Arch Gen Psychiatry, 28, 92, 10.1001/archpsyc.1973.01750310070010
Sharp, 1994, Pseudochoreoathetosis: movements associated with loss of proprioception, Arch Neurol, 41, 1103, 10.1001/archneur.1994.00540230041010
Sheehy, 1982, Writer's cramp – a focal dystonia, Brain, 105, 461, 10.1093/brain/105.3.461
Shiang, 1993, Mutations in the a1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia, Nat Genet, 5, 351, 10.1038/ng1293-351
Shimura, 2000, Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase, Nat Genet, 25, 302, 10.1038/77060
Shimura, 2001, Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease, Science, 293, 263, 10.1126/science.1060627
Shy, 1960, A neurologic syndrome associated with orthostatic hypotension, Arch Neurol, 2, 511, 10.1001/archneur.1960.03840110025004
Sider, 1979, Galen on tremor, palpitation, spasm, and rigor: Galeni De tremore, palpitatione, convulsione, et rigore, Trans Stud Coll Physicians Phila, 1, 183
Siderowf, 1998, Posey and Spiller and progressive supranuclear palsy: an incorrect attribution, Mov Disord, 13, 170, 10.1002/mds.870130133
Siegfried, 1994, Chronic electrical stimulation of the VL-VPL complex and of the pallidum in the treatment of extrapyramidal and cerebellar disorders. Personal experience since 1985, Stereotact Funct Neurosurg, 62, 71, 10.1159/000098599
Siegfried, 1994, Bilateral chronic electrostimulation of ventroposterolateral pallidum: a new therapeutic approach for alleviating all parkinsonian symptoms, Neurosurgery, 35, 1126, 10.1227/00006123-199412000-00016
Siemerling, 1922, Pseudosklerose (Westphal-Strumpell) mit Cornealring (Kayser-Fleischer) unter doppelseitiger Scheinkatarakt, die nur bei Seitlicherbeleuchtung sichtbar ist und die, der nach Verletzung durch kupfersplitterentstehenden Katarakt ähnlich ist, Klin Wochenschr, 1, 1087, 10.1007/BF01771550
Simpson, 2008, Assessment: botulinum neurotoxin for the treatment of movement disorders (an evidence-based review). Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology, Neurology, 70, 1699, 10.1212/01.wnl.0000311389.26145.95
Singer, 1982, Dopaminergic dysfunction in Tourette syndrome, Ann Neurol, 12, 361, 10.1002/ana.410120408
Sinkler, 1895, Choreiform affections, 227
Slavin, 2004, Treatment of hemiballismus with stereotacticc pallidotomy. Case report and review of the literature, Neurosurg Focus, 17, E7, 10.3171/foc.2004.17.1.7
Smith, 1988, Neurons of the subthalamic nucleus in primates display glutamate but not GABA immunoreactivity, Brain Res, 453, 353, 10.1016/0006-8993(88)90177-1
Snell, 1993, Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease, Nat Genet, 4, 393, 10.1038/ng0893-393
Sokol, 1985, Orthotopic liver transplantation for acute fulminant Wilson disease, J Pediatr, 107, 549, 10.1016/S0022-3476(85)80016-0
Solly, 1864, Clinical lectures on scriveners' palsy, or the paralysis of writers: Lecture I, Lancet, ii, 709
Solly, 1865, Clinical lectures on scriveners' palsy, or the paralysis of writers: Lecture II, Lancet, i, 84, 10.1016/S0140-6736(02)69633-3
Solly, 1865, Clinical lectures on scriveners' palsy, or the paralysis of writers: Lecture III, Lancet, i, 113, 10.1016/S0140-6736(02)52480-6
1992, Guidelines for the diagnosis of rheumatic fever. Jones criteria, 1992 update, JAMA, 268, 2069, 10.1001/jama.1992.03490150121036
Speelman, 1998, Resurgence of functional neurosurgery for Parkinson's disease: a historical perspective, Mov Disord, 13, 582, 10.1002/mds.870130336
Spiegel, 1947, Stereotaxic apparatus for operations on the human brain, Science, 106, 349, 10.1126/science.106.2754.349
Spillantini, 1997, Alpha-synuclein in Lewy bodies, Nature, 388, 839, 10.1038/42166
Spillantini, 1998, Filamentous alpha-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies, Neurosci Lett, 251, 205, 10.1016/S0304-3940(98)00504-7
Spiller, 1905, The importance in clinical diagnosis of paralysis of associative movement of the eyeballs (Blick-Lahmung) especially of upward and downward associated movements, J Nerv Ment Dis, 32, 417, 10.1097/00005053-190507000-00001
Squitieri, 2003, Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course, Brain, 126, 946, 10.1093/brain/awg077
Steck, 1954, Le syndrome extrapyramidal et diencephalique au cours des traitments au largactil et au serpasil, Ann Med Psychol (Paris), 112, 737
Steele, 1972, Progressive supranuclear palsy, Brain, 95, 693
Steele, 1994, Historical notes, J Neural Transm Suppl, 42, 3, 10.1007/978-3-7091-6641-3_1
Steele, 1964, Progressive supranuclear palsy, Arch Neurol, 10, 333, 10.1001/archneur.1964.00460160003001
Stine, 1993, Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15, Hum Molec Genet, 2, 1547, 10.1093/hmg/2.10.1547
Stollerman, 1997, Changing streptococci and prospects for the global eradication of rheumatic fever, Perspect Biol Med, 40, 165, 10.1353/pbm.1997.0044
Suarez, 1997, Pallidotomy for hemiballismus: efficacy and characteristics of neuronal activity, Ann Neurol, 42, 807, 10.1002/ana.410420519
Suhren, 1966, Hyperexplexia: a hereditary startle syndrome, J Neurol Sci, 3, 577, 10.1016/0022-510X(66)90047-5
Sweeney, 1997, What's in a name? Dr. Lewey and the Lewy body, Neurology, 49, 629, 10.1212/WNL.49.2.629
Sydenham, 1686
Sydenham, 1848, On St. Vitus's dance, 257
Tanzi, 1993, The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene, Nat Genet, 5, 344, 10.1038/ng1293-344
Taranta, 1956, The relationship of Sydenham's chorea to infection with Group A streptococci, Am J Med, 20, 170, 10.1016/0002-9343(56)90186-3
Telenius, 1993, Molecular analysis of juvenile Huntington's disease: the major influence on (CAG)n repeats length is the sex of affected parents, Hum Mol Genet, 2, 1535, 10.1093/hmg/2.10.1535
Telenius, 1994, Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm, Nat Genet, 6, 409, 10.1038/ng0494-409
Telenius, 1995, Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease, Hum Mol Genet, 4, 189, 10.1093/hmg/4.2.189
1993, Definitions and classification of tic disorders, Arch Neurol, 50, 1013, 10.1001/archneur.1993.00540100012008
Tiemann, 1899, 712
Todd, 1932, Antigenic streptococcal hemolysin, J Exp Med, 55, 267, 10.1084/jem.55.2.267
Tomonaga, 1977, Ultrastructure of neurofibrillary tangles in progressive supranuclear palsy, Acta Neuropathol (Berl), 37, 1771, 10.1007/BF00692065
Trétiakoff, 1919
Trétiakoff, 1921, Contribution à l'étude de l'anatomie du locus niger, Rev Neurol (Paris), 28, 592
Trottier, 1994, Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset, J Med Genet, 31, 377, 10.1136/jmg.31.5.377
Truong, 1988, An early description of dystonia: translation of Schwalbe's thesis and information on his life, Adv Neurol, 50, 651
Tschermak von Seysenegg, 1900, Über künstliche Kreuzung bei Pisum sativum, Zeitschrift für das Landwirthschaftliche Versuchswesen in Oesterreich, 3, 465
Tsui, 1985, A pilot study on the use of botulinum toxin in spasmodic torticollis, Can J Neurol Sci, 12, 314, 10.1017/S031716710003540X
Tsui, 1986, Double-blind study of botulinum toxin in spasmodic torticollis, Lancet, 2, 245, 10.1016/S0140-6736(86)92070-2
Tsui, 1987, Local treatment of spasmodic torticollis with botulinum toxin, Can J Neurol Sci, 14, 533, 10.1017/S0317167100038063
Tu, 1998, Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein, Ann Neurol, 44, 415, 10.1002/ana.410440324
Ueda, 1993, Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease, Proc Natl Acad Sci USA, 90, 11282, 10.1073/pnas.90.23.11282
Uhrbrand, 1960, Reversible and irreversible dyskinesia after treatment with perphenazine, chlorpromazine, reserpine, and electroconvulsive therapy, Psychopharmacologia, 1, 408, 10.1007/BF00441188
Unverricht, 1891
Uzman, 1956, The mechanism of copper deposition in the liver in hepatolenticular degeneration (Wilson's disease), Am J Med Sci, 231, 511, 10.1097/00000441-195605000-00004
Van Putten, 1975, The many faces of akathisia, Compr Psychiatry, 16, 43, 10.1016/0010-440X(75)90019-X
Vesalius, 1542, De Humani Corporis Fabrica, J Oporini, Basel
Vidailhet, 2005, Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia, N Engl J Med, 352, 459, 10.1056/NEJMoa042187
Vilensky, 2002, Denny-Brown, Wilson's disease, and BAL (British antilewisite [2,3-dimercaptopropanol]), Neurology, 59, 914, 10.1212/WNL.59.6.914
Vogt, 1929, Kupfer und Silber aufgespeichert in Auge, Leber, Milz und Nieren als Symptom der Pseudosklerose, Klin Monatsbl Augenheilkd, 83, 417
Vogt, 1920, Zur Lehre der Erkrankungen des striaren Systeme, Journal für Psychologie und Neurologie, 25, 627
von Economo, 1917, Encephalitis Lethargica, Wien Klin Wochenschr, 30, 581
von Economo, 1918
von Economo, 1929
von Economo, 1931
von Strümpel, 1898, Über die Westphal'sche Pseudosklerose und über diffuse Hirnsklerose insbesondere bei Kindern, Dtsch Z Nervenheilkd, 12, 115, 10.1007/BF02456569
Vonsattel, 1985, Neuropathological classification of Huntington's disease, J Neuropathol Exp Neurol, 44, 559, 10.1097/00005072-198511000-00003
Wakabayashi, 1998, Alpha-synuclein immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy, Neurosci Lett, 249, 180, 10.1016/S0304-3940(98)00407-8
Walshe, 1920, On the symptom complexes of lethargic encephalitis with special reference to the involuntary muscular contractions, Brain, 43, 197, 10.1093/brain/43.3.197
Walshe, 1956, Penicillamine, a new oral therapy for Wilson's disease, Am J Med, 21, 487, 10.1016/0002-9343(56)90066-3
Walshe, 1960, The treatment of Wilson's disease with penicillamine, Lancet, 1, 188, 10.1016/S0140-6736(60)90109-4
Walshe, 1962, Wilson's disease: the presenting symptoms, Arch Dis Child, 37, 253, 10.1136/adc.37.193.253
Walshe, 1968, Toxic reactions to penicillamine in patients with Wilson's disease, Postgrad Med J (Suppl), 6
Walshe, 1982, Treatment of Wilson's disease with trientine (triethylene tetramine) dichloride, Lancet, 1, 643, 10.1016/S0140-6736(82)92201-2
Walshe, 2003, The story of penicillamine: a difficult birth, Mov Disord, 18, 853, 10.1002/mds.10458
Walshe, 2006, History of Wilson's disease: 1912 to 2000, Mov Disord, 21, 142, 10.1002/mds.20694
Wasmuth, 1988, A highly polymorphic locus very tightly linked to the Huntington's disease gene, Nature, 332, 734, 10.1038/332734a0
Waters, 1842, 312
West, 1861, On a peculiar form of infantile convulsions, Lancet, i, 724
Westphal, 1883, Über eine dem Bilde der cerebrospinalen grauen Degeneration ähnliche Erkrankung des centralen Nervensystems ohne anatomischen Befund, nebst einigen Bemerkungen über paradoxe Contraktion, Arch Psychiatr Nervenkr, 14, 87, 10.1007/BF02004266
Wexler, 1987, Homozygotes for Huntington's disease, Nature, 326, 194, 10.1038/326194a0
Whittier, 1947, Ballism and subthalamic nucleus (nucleus hypothalamicus; corpus Luysi). Review of the literature and study of thirty cases, Arch Neurol Psychiatry, 58, 672, 10.1001/archneurpsyc.1947.02300350022002
Whittier, 1949, Studies on the subthalamus of the rhesus monkey. I. Anatomy and fiber connections of the subthalamic nucleus of Luys, J Comp Neurol, 90, 281, 10.1002/cne.900900303
Whittier, 1949, Studies on the subthalamus of the rhesus monkey. II. Hyperkinesia and other physiologic effects of subthalamic lesions, with special reference to the subthalamic nucleus of Luys, J Comp Neurol, 90, 319, 10.1002/cne.900900304
Wichmann, 1998, Models of basal ganglia function and pathophysiology of movement disorders, Neurosurg Clin N Am, 9, 223, 10.1016/S1042-3680(18)30261-4
Willis, 1685, 413
Wilson, 1911
Wilson, 1912, Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, Brain, 34, 295, 10.1093/brain/34.4.295
Wilson, 1912, Progressive lenticular degeneration: a familial nervous disease associated with cirrhosis of the liver, Lancet, 1, 1115, 10.1016/S0140-6736(01)67414-2
Wilson, 1912, Dégénération lenticulaire progressive: maladie familiale associée à la cirrhose du foie, Rev Neurol (Paris), 23, 229
Wilson, 1914, Progressive Degeneration des Linsenkerns, 950
Wilson, 1925, Disorders of motility and muscle tone with special reference to the corpus striatum (Croonian Lectures), Lancet, 2, 215
Winkler, 1974, Efficacy of chronic propranolol therapy in action tremors of the familial, senile or essential varieties, N Engl J Med, 290, 984, 10.1056/NEJM197405022901802
Winslow, 1986, Prevention of acute dystonic reactions in patients beginning high-potency neuroleptics, Am J Psychiatry, 143, 706
Yahr, 1969, Treatment of parkinsonism with levodopa, Arch Neurol, 21, 343, 10.1001/archneur.1969.00480160015001
Yang, 2002, Aggregated polyglutamine peptides delivered to nuclei are toxic to mammalian cells, Hum Molec Genet, 11, 2905, 10.1093/hmg/11.23.2905
Yoon, 2003, Huntington disease expansion mutations in humans can occur before meiosis is completed, Proc Natl Acad Sci USA, 100, 8834, 10.1073/pnas.1331390100
Young, 1986, Asterixis: one type of negative myoclonus, Adv Neurol, 43, 137
Young, 1976, Unilateral asterixis produced by a discrete CNS lesion, Trans Am Neurol Assoc, 101, 306
Zabel, 1986, Mapping of the DNA locus D4S10 and the linked Huntington's disease gene to 4p16-p15, Cytogenet Cell Genet, 42, 187, 10.1159/000132276
Zeman, 1970, Pathology of the torsion dystonias (dystonia musculorum deformans), Neurology, 20, 79, 10.1212/WNL.20.11_Part_2.79
Zeman, 1967, Dystonia musculorum deformans: clinical, genetic and pathoanatomical studies, Psychiatr Neurol Neurochir, 70, 77
Zeman, 1959, Idiopathic dystonia musculorum deformans. I. The hereditary pattern, Am J Hum Genet, 11, 188
Zeman, 1960, Idiopathic dystonia musculorum deformans. II. The formes frustes, Neurology, 10, 1068, 10.1212/WNL.10.12.1068
Zesiewicz, 2005, Practice parameter: therapies for essential tremor: report of the Quality Standards Subcommittee of the American Academy of Neurology, Neurology, 64, 2008, 10.1212/01.WNL.0000163769.28552.CD
Ziehen, 1911, Ein Fall von tonischer Torsionsneurose, Neurologisches Zentralblatt, 30, 109
Zoghbi, 2000, Glutamine repeats and neurodegeneration, Annu Rev Neurosci, 23, 217, 10.1146/annurev.neuro.23.1.217
Zuhlke, 1993, Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene, Hum Molec Genet, 2, 2063, 10.1093/hmg/2.12.2063
