References

Beaumanoir A, Mira L, van Lierde A. Epilepsy or paroxysmal kinesigenic choreoathetosis? Brain Dev. 1996;18:139-141.

Bennett LB, Roach ES, Bowcock AM. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16. Neurology. 2000;54:125-130.

Berkovic SF. Paroxysmal movement disorders and epilepsy. Links across the channel. Neurology 2000;55:169-170.

Bhatia KP. The paroxysmal dyskinesias. J Neurol. 1999;246:149-155.

Biary N, Singh B, Bahou Y, al Deeb SM, Sharif H. Posttraumatic paroxysmal nocturnal hemidystonia. Mov Disord. 1994;9:98-99.

Bressman SB, Fahn S, Burke RE. Paroxysmal non-kinesigenic dystonia. Adv Neurol. 1988;50:403-413.

Carrilho PE, Barbosa ER, Haddad MS, Comerlatti LR, Limongi JC, Scaff M. Kinesigenic paroxysmal choreoathetosis. Report of a case treated with carbamazepine [in Portugese]. Arq Neuropsiquiatr. 1994;52:414-418.

Demirkiran M, Jankovic J. Paroxysmal dyskinesias. In: Appel SH, ed. Current Neurology. Vol 16. Chicago, IL: Mosby Year Book; 1996:16:213-251.

Demirkiran M, Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol. 1995;38:571-579.

Fahn S. The paroxysmal dyskinesias. In: Marsden CD, Fahn S, eds. Movement Disorders 3. Oxford, England: Butterworth-Heinemann Ltd.; 1994:310-345.

Fegers S. Paroxysmal choreoathetosis [in German]. Fortschr Neurol Psychiatr. 1991;59:234-238.

Fink JK, Rainier S, Wilkowski J, et al. Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. Am J Hum Genet. 1996;59:140-145.

Forssman H. Hereditary disorder characterized by attacks of muscular contractions, induced by alcohol amongst other factors. Acta Med Scand. 1961;170:517-533.

Fouad GT, Servidei S, Durcan S, Bertini E, Ptacek LJ. A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet. 1996;59:135-139.

Gambardella A, Annesi G, Fusco MD, et al. A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1. Neurology 2000;55:1467-1471.

Goodenough DJ, Fariello RG, Annis BL, Chun RWM. Familial and acquired paroxysmal dyskinesias: a proposed classification with delineation of clinical features. Arch Neurol. 1978;35:827-831.

Hirata K, Katayama S, Saito T, et al. Paroxysmal kinesigenic choreoathetosis with abnormal electroencephalogram during attacks. Epilepsia 1991;32:492-494.

Houser MK, Soland VL, Bhatia KP, Quinn NP, Marsden CD. Paroxysmal kinesigenic choreoathetosis: a report of 26 patients. J Neurol. 1999;246:120-126.

Jarman PR, Bhatia KP, Davie C, et al. Paroxysmal dystonic choreoathetosis: Clinical features and investigation of pathophysiology in a large family. Mov Disord 2000;15:648-657.

Kertesz A. Paroxysmal kinesigenic choreoathetosis. Neurology 1967;17:680-690.

Kinast M, Erenberg G, Rothner AD. Paroxysmal choreoathetosis: report of five cases and review of the literature. Pediatrics. 1980;65:74-77.

Kitagawa N, Hayashi M, Akiguchi I, Kimura J. Ictal 99mTC-HMPAO-SPECT in a case of paroxysmal kinesigenic choreoathetosis [in Japanese]. Rinsho Shinkeigaku. 1998;38:767-770.

Kotagal P, Luders H, Morris HH, et al. Dystonic posturing in complex partial seizures of temporal lobe onset: a new lateralizing sign. Neurology. 1989;39:196-201.

Kurlan R, Behr J, Medved L, Shoulson I. Familial paroxysmal dystonic choreoathetosis: a family study. Mov Disord. 1987;2:187-192.

Kurlan R, Shoulson I. Familial paroxysmal dystonic choreoathetosis and response to alternate-day oxazepam therapy. Ann Neurol. 1983;13:456-457.

Lehkuniec E, Micheli F, De Arbelaiz R, Torres M, Paradiso G. Concurrent hypnogenic and reflex paroxysmal dystonia. Mov Disord. 1988;3:290-294.

Lugaresi E, Cirignotta F, Montagna P. Nocturnal paroxysmal dystonia. J Neurol Neurosurg Psychiatry. 1986;49:375-380.

Loher TJ, Krauss JK, Burgunder J-M, Taub E, Siegfried J. Chronic thalamic stimulation for treatment of dystonia paroxysmal nonkinesigenic dyskinesia. Neurology 2001;56:268-270.

Matsuo H, Kamakura K, Saito M, et al. Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2q. Arch Neurol. 1999;56:721-726.

Matsuo H, Okano M, Kaida K, Tadano Y, Kamakura K. A Japanese family with paroxysmal dystonic choreoathetosis [in Japanese]. Rinsho Shinkeigaku. 1997;37:905-909.

Münchau A, Valente EM, Shahidi GA, et al. A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study. J Neurol Neurosurg Psychiatry 2000;68:609-614.

Nagamitsu S, Matsuishi T, Hashimoto K, et al. Multicenter study of paroxysmal dyskinesias in Japan--clinical and pedigree analysis. Mov Disord. 1999;14:658-663.

Nardocci N, Lamperti E, Rumi V, Angelini L. Typical and atypical forms of paroxysmal choreoathetosis. Dev Med Child Neurol. 1989;31:670-674.

Newton MR, Berkovic SF, Austin MC, Reutens DC, Mckay WJ, Bladin PF. Dystonia, clinical lateralization, and regional blood flow changes in temporal lobe seizures. Neurology. 1992;42:371-377.

Online Mendelian Inheritance in Man (OMIM)™. National Center for Biotechnology Information Web site. John Hopkins University; McKusick VA, ed. 128200: Paroxysmal kinesigenic choreoathetosis; PKC. Available at: http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?128200. Accessed March 15, 2001.

Online Mendelian Inheritance in Man (OMIM)™. National Center for Biotechnology Information Web site. John Hopkins University; McKusick VA, ed. 118800: Paroxysmal nonkinesigenic dyskinesia; PNKD. Available at: http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?118800. Accessed March 15, 2001.

Online Mendelian Inheritance in Man (OMIM)™. National Center for Biotechnology Information Web site. John Hopkins University; McKusick VA, ed. 602066: Infantile convulsions and paroxysmal choreoathetosis, familial. Available at: http://www.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?602066. Accessed March 15, 2001.

Phillips HA, Marini C, Scheffer IE, et al. A de novo mutation in sporadic nocturnal frontal lobe epilepsy. Ann Neurol 2000;48:264-267.

Plant G. Focal paroxysmal kinesigenic choreoathetosis. J Neurol Neurosurg Psychiatry. 1983;46:345-348.

Plant GT, Williams AC, Earl CJ, Marsden CD. Familial paroxysmal dystonia induced by exercise. J Neurol Neurosurg Psychiatry. 1984;47:275-279.

Przuntek H, Monninger P. Therapeutic aspects of kinesiogenic paroxysmal choreoathetosis and familial paroxysmal choreoathetosis of the Mount and Reback type. J Neurol. 1983;230:163-169.

Ptacek LJ. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system. Neuromuscul Disord. 1997;7:250-255.

Ptacek LJ. Ligand-gated ion channelopathies. Mutations in different genes causing one disease. Neurology 2000;55:1429-1430.

Raskind WH, Bolin T, Wolff J, et al. Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34. Hum Genet. 1998;102:93-97.

Richardson JC, Howes JL, Celinski MJ, Allman RG. Kinesigenic choreoathetosis due to brain injury. Can J Neurol Sci. 1987;14:626-628.

Sadamatsu M, Masui A, Sakai T, Kunugi H, Nanko S, Kato N. Familial paroxysmal kinesigenic choreoathetosis: an electrophysiologic and genotypic analysis. Epilepsia. 1999;40:942-949.

Sethi KD, Hess DC, Huffnagle VH, Adams RJ. Acetazolamide treatment of paroxysmal dystonia in central demyelinating disease. Neurology. 1992;42:919-921.

Sethi KD. Paroxysmal dyskinesias. Neurologist 2000;6:177-185.

Swoboda KJ, Soong BW, McKenna C, et al. Paroxysmal kinesigenic dyskinesia and infantile convulsions. Clinical and linkage studies. Neurology 2000;55:224-230.

Tan LC, Tan AK, Tjia H. Paroxysmal kinesigenic choreoathetosis in Singapore and its relationship to epilepsy. Clin Neurol Neurosurg. 1998;100:187-192.

Tomita H, Nagamitsu S, Wakui K, et al. Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1. Am J Hum Genet. 1999;65:1688-1697.

Urasaki E, Tokimura T, Genmoto T, Yokota A. Paroxysmal kinesigenic choreoathetosis associated with frontotemporal arachnoid cyst--case report. Neurol Med Chir (Tokyo). 1999;39:169-173.

Valente EM, Spacey SD, Wali GM, et al. A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16. Brain 2000;123:2040-2045.

Wali GM. Paroxysmal hemidystonia induced by prolonged exercise and cold. J Neurol Neurosurg Psychiatry. 1992;55:236-237.

Wang BJ, Chang YC. Therapeutic blood levels of phenytoin in treatment of paroxysmal choreoathetosis. Ther Drug Monit. 1985;7:81-82.

Wein T, Andermann F, Silver K, et al. Exquisite sensitivity of paroxysmal kinesigenic choreoathetosis to carbamazepine. Neurology. 1996;47:1104-1106.