Laboratory diagnosis of hyperkinetic movement disorders in adults;Labordiagnostik hyperkinetischer bewegungsstörungen des erwachsenenalters

Nervenarzt

Volumn 73, Issue 2, 2002, Pages 133-143

  Laubis Herrmann, U ^a   Topka, H ^a,b  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b KLINIKUM BOGENHAUSEN   (Germany)

Author keywords

Etiology; Hyperkinetic movement disorders; Laboratory studies

Indexed keywords

CHOREA; DYSTONIA; HUMAN; HYPERKINESIA; IMAGING; LABORATORY DIAGNOSIS; MOTOR DYSFUNCTION; MYOCLONUS; REVIEW; TIC; TREMOR; CROSS-SECTIONAL STUDY; GENETIC MARKER; GENETIC SCREENING; PREDICTION AND FORECASTING; RISK FACTOR;

BIOLOGICAL MARKER;

BIOLOGICAL MARKERS; CROSS-SECTIONAL STUDIES; GENETIC MARKERS; GENETIC SCREENING; HUMANS; HYPERKINESIS; PREDICTIVE VALUE OF TESTS; RISK FACTORS;

EID: 0036483030     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00115-001-1256-1     Document Type: Review

References (134)

1. Anouti A, Koller WC (1996) Diagnostic testing in movement disorders. Neurol Clin 14:169-182
2. Fahn S (1998) Concept and classification of dystonia. Adv Neurol 50:1-8
3. Hartmann A, Pogarell O, Oertel WH (1998) Secondary dystonias. Neurology 245:511-518
4. Brooks DJ, Turjanski N, Sawle GV, Playford ED, Lees AJ (1992) PET studies on the integrity of the pre- and postsynaptic dopaminergic system in Tourette syndrome. Adv Neurol 58:227-231
5. Van de Wetering BJ, Heutink P (1993) The genetics of the Gilles de la Tourette syndrome: a review. J Lab Clin Med 121:638-645
6. Singer HS, Giuliano JD, Hansen BH, Hallett JJ, Laurino JP, Benson M, Kiessling LS (1998) Antibodies against human putamen in children with Tourette syndrome. Neurology 50:1618-1624
7. Swedo SE, Leonard HL, Kiessling LS (1994) Speculations on antineuronal antibody-mediated neuropsychiatric disorders of childhood. Pediatrics 93:323-326
8. Hoogstraten MC, Lakke JP, Zwarts MJ (1986) Bilateral ballism: a rare syndrome. Review of the literature and presentation of a case. J Neurol 233:25-29
9. Weindl A, Conrad B (1996) Chorea und choreatische Bewegungsstö rungen. In: Conrad B, Ceballos-Baumann AO (Hrsg) Bewegungsstörungen in der Neurologie. Georg Thieme, Stuttgart New York, S. 155-180
10. Topka H, Dichgans J (1998) Dyskinesien. In: Brandt T, Dichgans J, Diener HC (Hrsg) Therapie und Verlauf neurologischer Krankheiten. Kohlhammer, Stuttgart Berlin Köln, S 889-914
11. Conrad B (1996) Hemiballismus/Ballismus. In: Conrad B, Ceballos-Baummann AO (Hrsg) Bewegungsstörungen in der Neurologie. Georg Thieme, Stuttgart New York, S 181-185
12. Marsden C, Hallett M, Fahn S (1981) The nosology and pathophysiology of myoclonus. In: Marsden CD, Fahn S (eds) Neurology 2 - Movement disorders. Butterworth Scientific, London, pp 196-248
13. Nutt JG, Muenter MD, Aronson A, Kurland LT, Melton LJD (1988) Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord 3:188-194
14. Reilly M, Daly L, Hutchinson M (1993) An epidemiological study of Wilson's disease in the Republic of Ireland. J Neurol Neurosurg Psychiatry 56:298-300
15. Lossner J, Bachmann H, Siegemund R, Kuhn HJ, Gunther K (1990) Wilson's disease in East Germany: in retrospect and perspectives - an evaluation. Psychiatr Neurol Med Psychol Leipz 42:585-600
16. Nygaard TG (1993) Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis. Adv Neurol 60:577-585
17. Knappskog PM, Flatmark T, Mallet J, Ludecke B, Bartholome K (1995) Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381 K) in the tyrosine hydroxylase gene. Hum Mol Genet 4:1209-1212
18. Ichinose H, Suzuki T, Inagaki H, Ohye T, Nagatsu T (1999) Molecular genetics of dopa-responsive dystonia. Biol Chem 380:1355-1364
19. Rondot P, Wevers RA (1999) Recessive dopa-responsive form of dystonia due to a mutation of the tyrosine hydroxylase gene. Bull Acad Natl Med 183:639-646
20. Van den Heuvel LP, Luiten B, Smeitink JA et al. (1998) A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population. Hum Genet 102:644-646
21. Hwu WL, Wang PJ, Hsiao KJ, Wang TR, Chiou YW, Lee YM (1999) Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation. Hum Genet 105:226-230
22. Aasly J, Skandsen T, Ro M (1999) Neuroacanthocytosis - the variability of presenting symptoms in two siblings. Acta Neurol Scand 100:322-325
23. Miranda M, Campero M, Tenhamm E, Villagra R (1993) Neuroacanthocytosis: report of 3 cases. Rev Med Chil 121:176-179
24. Hardie RJ, Pullon HW, Harding AE et al. (1991) Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases. Brain 114:13-49
25. Peppard RF, Lu CS, Chu NS, Teal P, Martin WR, Calne DB (1990) Parkinsonism with neuroacanthocytosis. Can J Neurol Sci 17:298-301
26. De Yebenes JG, Brin MF, Mena MA et al. (1988) Neurochemical findings in neuroacanthocytosis. Mov Disord 3:300-312
27. Yamamoto K, Kawazawa S (1987) Basal ganglion calcification in paroxysmal dystonic choreoathetosis. Ann Neurol 22:556
28. Siejka SJ, Knezevic WV, Pullan PT (1988) Dystonia and intracerebral calcification: pseudohypoparathyroidism presenting in an eleven-year-old girl. Aust N Z J Med 18:607-609
29. Lauterbach EC, Spears TE, Prewett MJ, Price ST, Jackson JG, Kirsh AD (1994) Neuropsychiatric disorders, myoclonus, and dystonia in calcification of basal ganglia pathways. Biol Psychiatry 35:345-351
30. Nishiyama K, Honda E, Mizuno T, Sakuta M, Kawakami H (1991) A case of idiopathic, symmetrical non-arteriosclerotic, intracerebral calcification (Fahr's disease) associated with M-proteinemia, followed by multiple myeloma. Rinsho Shinkeigaku 31:781-784
31. Klein C, Vieregge P, Kompf D (1997) Paroxysmal choreoathetosis in a patient with idiopathic basal ganglia calcification, chorea, and dystonia. Mov Disord 12:254-255
32. Di Rocco M (1986) Dystonia and calcification of the basal ganglia: another case. Neurology 36:306
33. Larsen TA, Dunn HG, Jan JE, Calne DB (1985) Dystonia and calcification of the basal ganglia. Neurology 35:533-537
34. Lucci B, Zucco R (1981) Striopallidodentate calcifications. Report of two cases. Riv Patol Nerv Ment 102:1-11
35. Caraceni T, Broggi G, Avanzini G (1974) Familial idiopathic basal ganglia calcification exhibiting "dystonia musculorum deformans" features. Eur Neurol 12:351-359
36. Bobek J, Nowak M (2000) Familial form of Fahr syndrome (report of two cases). Neurol Neurochir Pol 34:167-175
37. Prieto JM, Pardellas H, Sobrido MJ, Lema M, Dapena D, Castro A (1997) Familial striopallido-dentate calcification. Rev Neurol 25:1213-1215
38. Geschwind DH, Loginov M, Stern JM (1999) Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet 65:764-772
39. Cavalier L, Ouahchi K, Kayden HJ, DiDonato S, Reutenauer L, Mandel JM, Koenig M (1998) Ataxia with isolated vitamin E deficiency: Heterogeneity of mutations and phenotypic variability in a large number of families. Am J Hum Genet 62:301-310
40. Moore DP (1996) Neuropsychiatric aspects of Sydenham's chorea: a comprehensive review. J Clin Psychiatry 57:407-414
41. Bohlega S, Riley W, Powe J, Baynton R, Roberts G (1998) Neuroacanthocytosis and aprebetalipoproteinemia. Neurology 50:1912-1914
42. Schwartz MS, Monro PS, Leigh PN (1992) Epilepsy as the presenting feature of neuroacanthocytosis in siblings. J Neurol 239:261-262
43. Yamamoto T, Hirose G, Shimazaki K, Takado S, Kosoegawa H, Saeki M (1982) Movement disorders of familial neuroacanthocytosis syndrome. Arch Neurol 39:298-301
44. Gries P, Weindl A (1988) Epidemiologische Untersuchungen über die Huntington'sche Erkrankung in Bayern. In: Deuschl G, Oepen G, Wolf H (Hrsg) Die Huntington'sche Krankheit. Springer, Berlin Heidelberg New York, S 12-17
45. Quinn N, Schrag A (1998) Huntington's disease and other choreas. J Neurol 245:709-716
46. Ghram N, Allani C, Oudali B, Fitouri Z, Ben Becher S (1999) Sydenham's chorea in children. Arch Pediatr 6:1048-1052
47. Eshel G, Lahat E, Azizi E, Gross B, Aladjem M (1993) Chorea as a manifestation of rheumatic fever - a 30-year survey (1960-1990). Eur J Pediatr 152:645-646
48. Rinne A (1947) On the cond ition of patients with chorea minor in the light of follow-up examinations. Annales Medicinae Internae Fenniae 36:613-618
49. Swedo SE, Rapoport JL, Cheslow DL, Leonhard HL, Ayoub EM, Hosier DM, Wald ER (1989) High prevalence of obsessive-compulsive symptoms in patients with Sydenham's chorea. Am J Psychiatry 146:246-249
50. Sebastian GD, Galeazzi M, Tincani A et al. (1999) Anticardiolipin and anti-beta2GPI antibodies in a large series of European patients with systemic lupus erythematosus. Prevalence and clinical associations. European Concerted Action on the Immunogenetics of SLE. Scand J Rheumatol 28:344-351
51. Johnson AE, Gordon C, Hobbs FD, Bacon PA (1996) Undiagnosed systemic lupus erythematosus in the community. Lancet 347:367-369
52. Hochberg MC, Perlmutter DL, Medsger TA, Stehen V, Weisman MH, White B, Wigley FM (1995) Prevalence of self-reported physician-diagnosed systemic lupus erythematosus in the USA. Lupus 4:454-456
53. Wallace DJ, Quismorio FP Jr (1995) The elusive search for geographic clusters of systemic lupus erythematosus. Critical review. Arthritis Rheum 38:1564-1567
54. Gibson T, Myers AR (1975) Nervous system involvement in systemic lupus erythematosus. Ann Rheum Dis 35:398-406
55. Beresford O, Graham AM (1950) Chorea gravidarum. J Obstet Gynaecol Br Emp 57:616-625
56. Wilson P, Preece M (1932) Chorea gravidarum. Arch Intern Med 49:471-533
57. Nyman M, Durling U, Lundell A (1997) Chorea gravidarum. Acta Obstet Gynecol Scand 76:885-886
58. Dike GL (1997) Chorea gravidarum: a case report and review. MD Med J 46:436-439
59. Rebes Z, Oszukowski P, Wilczynski J, Lisiewicz J, Wendorff J (1996) Chorea gravidarum - case report. Ginekol Pol 67:574-576
60. Warner TT, Williams LD, Walker RW et al. (1995) A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families. Ann Neurol 37:452-459
61. Nielsen JE, Sorensen SA, Hasholt L, Norremolle A (1996) Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family. Mov Disord 11:533-541
62. Llamas Sillero P, Cabrera Marin R, Fernandez Rodriguez MN (1998) Generalized chorea as initial manifestation of polycythemia vera. Med Clin Barc 111:317-318
63. Chamouard JM, Smagghe A, Malalanirina BH, Davous P, Poisson M (1992) Chorea disclosing polycythemia and renal adenocarcinoma. Rev Neurol Paris 148:380-382
64. Cohen AM, Gelvan A, Yarmolovsky A, Djaldetti M (1989) Chorea in polycythemia vera: a rare presentation of hyperviscosity. Blut 58:47-48
65. Rigon G, Baratti M, Quaini F, Calzetti S (1987) Polycythemic chorea. Description of a clinical case. Minerva Med 78:1325-1329
66. Mas JL, Gueguen B, Bouche P, Derouesne C, Varet B, Castaigne P (1985) Chorea and polycythaemia. J Neurol 232:169-171
67. Piccolo I, Causarano R, Sterzi R et al. (1999) Chorea in patients with AIDS. Acta Neurol Scand 100:332-336
68. Maggi P, de Mari M, de Blasi R et al. (1996) Choreoathetosis in acquired immune deficiency syndrome patients with cerebral toxoplasmosis. Mov Disord 11:434-436
69. Iranzo A, Kulisevsky J, Cadafalch J, Serrano C, Grau JM (1996) Movement disorders and AIDS. Neurologia 11:70-75
70. Garretto NS, Bueri JA, Kremenchutzky M, Consalvo D, Segura M, Genovese O (1995) Hemichorea associated with cerebral toxoplasmosis and AIDS. Arq Neuropsiquiatr 53:118-122
71. Nath A, Hobson DE, Russell A (1993) Movement disorders with cerebral toxoplasmosis and AIDS. Mov Disord 8:107-112
72. Hammann KP, Henkel B, Erbel R, Kramer G (1985) Hemichorea associated with varicella-zoster reinfection and endocarditis. A case report. Eur Arch Psychiatry Neurol Sci 234:404-407
73. Leavell R, Ray CG, Ferry PC, Minnich LL (1986) Unusual acute neurologic presentations with Epstein-Barr virus infection. Arch Neurol 43:186-188
74. Isgreen WP, Chutorian AM, Fahn S (1976) Sequential parkinsonism and chorea following "mild" inluenza. Trans Am Neurol Assoc 101:56-60
75. Jones AL, Bouchier IA (1993) A patient with neurosyphilis presenting as chorea. Scott Med J 38:82-84
76. Brogan GX, Homan CS, Viccellio P (1990) The enlarging clinical spectrum of Lyme disease: Lyme cerebral vasculitis, a new disease entity. Ann Emerg Med 19:572-576
77. Reik L, Steere AC, Bartenhagen NH, Shope RE, Malawista SE (1979) Neurologic abnormalities of Lyme disease. Medicine Baltimore 58:281-294
78. Decaux G, Szyper M, Ectors M, Cornil A, Franken L (1980) Central nervous system complications of Mycoplasma pneumoniae. J Neurol Neurosurg Psychiatry 43:883-887
79. Schurmann D, Ruf B, Hertel G, Pohle HD (1986) Neurologic symptoms in Legionella infection. A case report of the clinical aspects and diagnosis of legionellosis. Nervenarzt 57:487-489
80. Cervera R, Asherson RA, Font J, Tikly M, Pallares L, Chamorro A, Ingelmo M (1997) Chorea in the antiphospholipid syndrome. Clinical, radiologic, and immunologic characteristics of 50 patients from our clinics and the recent literature. Medicine Baltimore 76:203-212
81. Nagaoka T, Matsushita S, Nagai Y, Kobayashi K (1998) A woman who trembled, then had chorea. Lancet 351:1326
82. Yen DJ, Shan DE, Lu SR (1998) Hyperthyroidism presenting as recurrent short paroxysmal kinesigenic dyskinesia. Mov Disord 13:361-363
83. Lucantoni C, Grottoli S, Moretti A (1994) Chorea due to hyperthyroidism in old age. A case report. Acta Neurol Napoli 16:129-133
84. Pozzan GB, Battistella PA, Rigon F, Zancan L, Casara GL, Pellegrino PA, Zacchelo F (1992) Hyperthyroid-induced chorea in an adolescent girl. Brain Dev 14:126-127
85. Shaw C, Haas L, Miller D, Delahunt J (1996) A case report of paroxysmal dystonic choreoathetosis due to hypoglycaemia induced by an insulinoma. J Neurol Neurosurg Psychiatry 61:194-195
86. Hefter H, Mayer P, Benecke R (1993) Persistent chorea after recurrent hypoglycemia. A case report. Eur Neurol 33:244-247
87. Oerlemans WG, Moll LC (1999) Non-ketotic hyperglycemia in a young woman, presenting as hemiballism-hemichorea. Acta Neurol Scand 100:411-414
88. Iwata A, Koike F, Arasaki K, Tamaki M (1999) Blood brain barrier destruction in hyperglycemic chorea in a patient with poorly controlled diabetes. J Neurol Sci 163:90-93
89. Lee BC, Hwang SH, Chang GY (1999) Hemiballismus-hemichorea in older diabetic women: a clinical syndrome with MRI correlation. Neurology 52:646-648
90. Piccolo I, Sterzi R, Thiella G (1998) Chorea in hyperglycemia. Diabetes Care 21:1777
91. Tranchant C, Bhatia KP, Marsden CD (1995) Movement disorders in multiple sclerosis. Mov Disord 10:418-423
92. Lee MS, Marsden CD (1994) Movement disorders following lesions of the thalamus or subthalamic region. Mov Disord 9:493-507
93. Masucci EF, Saini N, Kurtzke JF (1989) Bilateral ballism in multiple sclerosis. Neurology 39:1641-1642
94. Awada A (1993) Hemiballismus disclosing cerebral toxoplasmosis and acquired immunodeficiency syndrome. Rev Neurol Paris 149:421-423
95. Martinez Martin P (1990) Hemichorea-hemiballism in AIDS. Mov Disord 5:180
96. Krauss JK, Collard M, Mohadjer M, Etou A, Kiesmann M, Mundinger F (1990) Hemiballism as the primary symptom of AIDS. Nervenarzt 61:510-515
97. Sanchez Ramos JR, Factor SA, Weiner WJ, Marquez J (1989) Hemichorea-hemiballismus associated with acquired immune deficiency syndrome and cerebral toxoplasmosis. Mov Disord 4:266-273
98. Nath A, Jankovic J, Pettigrew LC (1987) Movement disorders and AIDS. Neurology 37:37-41
99. Thompson SW (1976) Ballistic movements of the arm in systemic lupus erythematosis. Dis Nerv Syst 37:331-332
100. Havsager AM, Carstensen NC (1991) Ballism in systemic lupus erythematodes Ugeskr Laeger 153:2301-2302
101. Namer IJ, Tan E, Akalin E, Selekler K, Zileli T (1990) A case of hemiballismus during cryptococcal meningitis. Rev Neurol Paris 146:153-154
102. Barthez Carpentier MA, Rozenberg F et al. (1995) Relapse of herpes simplex encephalitis. J Child Neurol 10:363-368
103. Odaka M, Yuki N, Hirata K (1999) Bilateral ballism in a patient with overlapping Fisher's and Guillain-Barre syndromes. J Neurol Neurosurg Psychiatry 67:206-208
104. Lai PH, Tien RD, Chang MH et al. (1996) Chorea-ballismus with nonketotic hyperglycemia in primary diabetes mellitus. Am J Neuroradiol 17:1057-1064
105. Salomez JL, Francois M, Petit H (1982) Hemiballism in Behcet's syndrome. Larc Med 2:869-870
106. Kontogiannis V, Powell RJ (2000) Behcet's disease. Postgrad Med J 76:629-637
107. Schulz J (1998) Metabolische und toxische Enzephalopathien. In: Brandt T DJ, Diener HC (Hrsg) Therapie und Verlauf neurologischer Krankheiten. Kohlhammer, Stuttgart Berlin Köln, S 811-822
108. Lange U, Teichmann J, Doppl W, Klor H (1998) Whipple's disease - current status of diagnostics and therapy. Eur J Med Res 3:331-339
109. Pfister H (1998) Bakterielle Infektionen. In: Brandt T, Dichgans J, Diener HC (Hrsg) Therapie und Verlauf neurologischer Krankheiten. Kohlhammer, Stuttgart Berlin Köln, S 389-406
110. Parchi P, Castellani R, Capellari S et al. (1996) Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 39:767-778
111. Masullo C, Pocchiari M, Neri G, Cassacia P, Iavarone A, Ladogana A, Macchi G (1988) A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986). Eur J Epidemiol 4:482-487
112. Pals P, Van Everbroeck B, Sciot R et al. (1999) A retrospective study of Creutzfeldt-Jakob disease in Belgium. Eur J Epidemiol 15:517-519
113. Urushitani M, Wakita H, Ikeda A, Akiguchi I, Shibasaki H, Kimura J (1993) Chronic herpes simplex encephalitis initially presenting with persistent myoclonus. Rinsho Shinkeigaku 33:880-885
114. Baquero M, Narciso ML, Garcia M, Perla C, Dominguez F (1995) Celiac disease with occipital calcifications: 2 late cases. Med Clin Barc 105:781-783
115. Bhatia KP, Brown P, Gregory R et al. (1995) Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum. Brain 118:1087-1093
116. Tison F, Arne P, Henry P (1989) Myoclonus and adult coeliac disease. J Neurol 236:307-308
117. Finelli PF, McEntee WJ, Ambler M, Kestenbaum D (1980) Adult celiac disease presenting as cerebellar syndrome. Neurology 30:245-249
118. Berkovic SF, Carpenter S, Andermann F, Andermann E, Wolfe LS (1988) Kufs' disease: a critical reappraisal. Brain 111:27-62
119. Fujita N, Kimura T, Matsubara N, Tabe H, Tanaka K (1999) A case of adult neuronal ceroid lipofuscinosis type A. Rinsho Shinkeigaku 39:478-480
120. Yoshioka A, Saiki S, Yamaya Y, Kanemoto M, Hirose G (1999) A 54-year-old man with action myoclonus, parkinsonism and epilepsy. No To Shinkei 51:999-1007
121. Tana T, Komine Y, Kanzato N, Kawazoe N, Fukiyama K (1995) Two siblings with adult-onset sialidosis type I (cherry-red spot-myoclonus syndrome). Rinsho Shinkeigaku 35:803-805
122. Nishiyama Y, Sakamoto S, Katayama Y, Mishina M, Terashi A (1997) Neuroradiological findings on cerebral blood flow and metabolism of a case of adult onset sialidosis. Rinsho Shinkeigaku 37:982-986
123. Mattle H (1985) Neurologic manifestations of osmolality disorders. Schweiz Med Wochenschr 115:882-889
124. Young RR, Shahani BT (1986) Asterixis: one type of negative myoclonus. Adv Neurol 43:137-156
125. Dumitriu L, Ursu H (1985) Hyperthyroidism in the elderly. Clinical manifestations. Endocrinologie 23: 83-90
126. Smith IS (1994) The natural history of chronic demyelinating neuropathy associated with benign IgM paraproteinaemia. A clinical and neurophysiological study. Brain 117: 949-957
127. Leger JM, Vaunaize J (1990) Polyneuropathy associated with IgM monoclonal gammopathy: a review. Clinical, electrophysiological and pathological features. Nouv Rev Fr Hematol 32: 303-306
128. Sommer N (1998) Entzündliche und infektiöse Polyneuropathien. In: Brandt T DJ, Diener HC (Hrsg) Therapie und Verlauf neurologischer Krankheiten. Kohlhammer, Stuttgart Berlin Köln, S 1025-1042
129. Yeung KB, Thomas PK, King RH et al. (1991) The clinical spectrum of perpiheral neuropathies associated with benign monoclonal IgM, IgG and IgA paraproteinaemia. Comparative clinical, immunological and nerve biopsy findings. J Neurol 238: 383-391
130. Pedersen SF, Pullman SL, Latov N, Brannagan TH (1997) Physiological tremor analysis of patients with anti-myelin-associated glycoprotein associated neuropathy and tremor. Muscle Nerve 20: 38-44
131. Shimizu N, Suzuki M, Yamaguchi Y, Aoki T, Matsuda I, Arima M (1996) A nation-wide survey for neurologic and hepato-neurologic type of Wilson disease: clinical features and hepatic copper content. No To Hattatsu 28: 391-397
132. Loudianos G, Gitlin JD (2000) Wilson's disease. Seminars in Liver Disease 20: 353-364
133. Wisser H (2000) Katecholamine, Katecholaminmetabolite. In: Thomas L (Hrsg) Labor und Diagnose. TH-Books-Verlagsgesellschaft, Frankfurt a. Main, S 1026-1075
134. Kruse-Jarres JD (2000) Toxische Metalle. In: Thomas L (Hrsg) Labor und Diagnose. TH-Books-Verlagsgesellschaft, Frankfurt a. Main, S 360-371