The electroencephalogram in acetazolamide-responsive periodic ataxia

Movement Disorders

Volumn 11, Issue 3, 1996, Pages 283-288

  Neufeld, M Y ^a   Nisipeanu, P ^b   Chistik, V ^b   Korczyn, A D ^b  

^a TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^b NONE

Author keywords

Acetazolamide responsive periodic ataxia; Electroencephalogram; Ictal recordings; Interictal recordings

Indexed keywords

ACETAZOLAMIDE;

ADOLESCENT; ADULT; ARTICLE; ATAXIA; CASE REPORT; CEREBELLAR ATAXIA; ELECTROENCEPHALOGRAM; FAMILIAL DISEASE; HUMAN; MALE; MOTOR DYSFUNCTION; NYSTAGMUS; PATHOPHYSIOLOGY; PRIORITY JOURNAL; VERTIGO;

ACETAZOLAMIDE; ADOLESCENT; ADULT; ANTICONVULSANTS; CEREBELLAR ATAXIA; CEREBRAL CORTEX; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS; HUMANS; MALE; MIDDLE AGED; NEUROLOGIC EXAMINATION; PERIODICITY;

EID: 0030005268     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.870110312     Document Type: Article

References (35)

1. Sogg RL, Hoyt WF. Intermittent vertical nystagmus in a father and son. Arch Ophthalmol 1963;68:515-517.
2. Farmer TW, Mustian VM. Vestibulocerebellar ataxia. Arch Neurol 1963;8:471-480.
3. Hill W, Sherman H. Acute intermittent familial cerebellar ataxia. Arch Neurol 1968;18:350-357.
4. White JC. Familial periodic nystagmus, vertigo and ataxia. Arch Neurol 1969;20:276-280.
5. Griggs RC, Moxley RT, Lafrance RA, McQuillen J. Hereditary paroxysmal ataxia; response to acetazolamide. Neurology 1978;28:1259-1264.
6. Donat JR, Auger R. Familial periodic ataxia. Arch Neurol 1979;36:568-569.
7. Margolin DI, Nutt JG, Lovrien EW. Familial periodic ataxia: clinical and genetic studies [Abstract]. Ann Neurol 1981,10:75.
8. Braham J, Siegal T, Sadeh M. Periodic ataxia: an unusual non-familial variation with paroxysmal EEG features. J Neurol 1982;227:55-59.
9. Zasorin NL, Baloh RW, Myers LB. Acetazolamide-responsive episodic ataxia syndrome. Neurology 1983;33: 1212-1214.
10. Aimard G, Vigetto A, Trillet M, Ventre JJ, Devic M. Ataxie paroxystique familiale sensible a l'acetazolamide. Rev Neurol 1983;139:251-257.
11. Bouchard JP, Roberge C, van Gelder NM, Barbeau A. Familial periodic ataxia responsive to acetazolamide. Can J Neurol Sci 1984;11:550-553.
12. Trillet M, Gouttard M, Schott B. Ataxie paroxystique familiale sensible a l'acetazolamide. Rev Neurol 1985,141:203-206.
13. Verlooy P, Velis DN. Non-familial periodic ataxia responding to acetazotamide. Clin Neurol Neurosurg 1985;87:35-37.
14. Farris BK, Smith JL, Ayyar R. Neuro-ophthalmologic findings in vestibulocerebellar ataxia. Arch Neurol 1986;43: 1050-1053
15. Gancher ST, Nutt JG. Autosomal dominant episodic ataxia: a heterogenous syndrome. Mov Disord 1986;1:239-253.
16. Friedman JH, Hollmann PA. Acetazolamide-responsive hereditary paroxysmal ataxia. Mov Disord 1987;2:67-82.
17. Koller W, Bahamon-Dussan J. Hereditary paroxysmal cerebellopathy: responsiveness to acetazolamide. Clin Neuropharmacol 1987;10:65-68.
18. Vighetto A, Froment JC, Trillet M, Aimard G. Magnetic resonance imaging in familial paroxysmal ataxia. Arch Neurol 1988;45:547-549.
19. Feeney GFX, Boyle RS. Paroxysmal cerebellar ataxia. Aust NZ J Med 1989;19:113-117.
20. Baloh RW, Winder A. Acetazolamide-responsive vestibulocerebellar syndrome: clinical and oculographic features. Neurology 1991;41:429-431.
21. Bain PG, O'Brien MD, Keevil SF, Porter DA. Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis. Ann Neurol 1992;31:147-154.
22. Hawkes CH. Familial paroxysmal ataxia: report of a family. J Neurol Neurosurg Psychiatry 1992;55:212-213.
23. Van Bogaert PV, Nechel CV, Szliwowski HB. EEG findings in a family with acetazolamide responsive paroxysmal ataxia. Neurology 1993;43:378.
24. Van Bogaert P, Van Nechel C, Goldman S, Szliwowski HB. Acetazolamide-responsive hereditary paroxysmal ataxia: a report of a new family. Acta Neurol Belg 1993;93:268-275.
25. Parker HL. Periodic ataxia. In: Hewlett RM, Nevling AB, Minor JR. et al. eds. Collected papers of the Mayo Clinic, vol. 38. Philadelphia: Saunders, 1946:642-645.
26. Salam M. Metabolic ataxias. In: Vinken PJ, Bruyn GW, eds. Handbook of clinical neurology, vol. 21. Amsterdam: NorthHolland, 1975:573-585.
27. Blass JP, Kark P, Engel WK. Clinical studies of a patient with pyruvate decarboxylase deficiency. Arch Neurol 1971; 25:449-460.
28. Evans OB, Kilroy AW, Fenichel GM. Acetazolamide in the treatment of pyruvate dysmetabolism syndromes. Arch Neurol 1978;35:302-305.
29. Livingstone IR, Gardner-Medwin D, Pennington RJT. Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and response to acetazolamide. J Neurol Sci 1984;64: 89-97.
30. Brunt ERP, Van Weerden TW. Familial paroxysmal kinesigenic ataxia and continuous myokymia. Brain 1990;113: 1361-1382.
31. Vaamonde J, Artieda J, Obeso JA. Hereditary paroxysmal ataxia with neuromyotonia. Mov Disord 1991;6:180-182.
32. Nespeca M, Evans OB, Rose J. Metabolic and anatomical abnormalities in familial intermittent ataxia. Neurology 1987;37:107.
33. Vahedi K, Joutel A, Van Bogaert P, et al. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p. Ann Neurol 1995;37:289-293.
34. Schaul N, Luders H, Sachdev K. Generalized bilateral synchronous bursts of slow waves in the EEG. Arch Neurol 1981;38:690-692.
35. Dow RS. Extrinsic regulatory mechanisms of seizure activity. Epilepsia 1965;6:122-140.