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REFERENCES

  • Aicardi J, Chevrie JJ. (1982) Atypical benign partial epilepsy of childhood. Developmental Medicine & Child Neurology 24:281292.
  • Commission on Classification and Terminology of the International League Against Epilepsy. (1989) Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 30:389399.
  • De Negri M. (1997) Electrical status epilepticus during sleep (ESES): different clinical syndromes: towards a unifying view? Brain & Development 19:447451.
  • De Tiege X, Goldman S, Laureys S, Verheulpen D, Chiron C, Wetzburger C, Paquier P, Chaigne D, Poznanski N, Jambaque I, Hirsch E, Dulac O, Van Bogaert P. (2004) Regional cerebral glucose metabolism in epilepsies with continuous spikes and waves during sleep. Neurology 63:853857.
  • Deonna T, Zesiger P, Davidoff V, Maeder M, Mayor C, Roulet E. (2000) Benign partial epilepsy of childhood: a longitudinal neuropsychological and EEG study of cognitive function. Developmental Medicine & Child Neurology 42:595603.
  • Doose H, Baier WK. (1989) Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation. European Journal of Pediatrics 149:152158.
  • Doose H, Brigger-Heuer B, Neubauer B. (1997) Children with focal sharp waves: clinical and genetic aspects. Epilepsia 38:788796.
  • Doose H, Hahn A, Neubauer BA, Pistohl J, Stephani U. (2001) Atypical “benign” partial epilepsy of childhood or pseudo-Lennox syndrome, Part II: family study. Neuropediatrics 32:913.
  • Feekery CJ, Parry-Fielder B, Hopkins IJ. (1993) Landau-Kleffner syndrome: six patients including discordant monozygotic twins. Pediatric Neurology 9:4953.
  • Saltik S, Uluduz D, Cokar O, Demirbilek V, Dervent A. (2005) A clinical and EEG study on idiopathic partial epilepsies with evolution into ESES spectrum disorders. Epilepsia 46:524533.
  • Scheffer IE, Jones L, Pozzebon M, Howell RA, Saling MM, Berkovic SF. (1995) Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation. Annals of Neurology 38:633642.
  • Tassinari CA, Rubboli G, Volpi L, Billard C, Bureau M. (2002) Electrical status epilepticus during slow sleep (ESES or CSWS) including acquired epileptic aphasia (Landau-Kleffner syndrome). In RogerJ, BureauM, DravetC, GentonP, TassinariCA, WolfP (Eds) Epileptic syndromes in infancy, childhood and adolescence. John Libbey, London , pp. 265283.
  • Tassinari CA, Rubboli G, Volpi L, Meletti S, D'Orsi G, Franca M, Sabetta AR, Riguzzi P, Gardella E, Zaniboni A, Michelucci R. (2000) Encephalopathy with electrical status epilepticus during slow sleep or ESES syndrome including the acquired aphasia. Clinical Neurophysiology 111(suppl 2):S94S102.
  • Vadlamudi L, Harvey AS, Connellan MM, Milne RL, Hopper JL, Scheffer IE, Berkovic SF. (2004) Is benign rolandic epilepsy genetically determined? Annals of Neurology 56:129132.
  • Van Bogaert P, Wikler D, Damhaut P, Szliwowski HB, Goldman S. (1998) Cerebral glucose metabolism and centrotemporal spikes. Epilepsy Research 29:123127.
  • Veggiotti P, Beccaria F, Guerrini R, Capovilla G, Lanzi G. (1999) Continuous spike-and-wave activity during slow-wave sleep: syndrome or EEG pattern? Epilepsia 40:15931601.