SEARCH

SEARCH BY CITATION

References

  • Agostinelli S, Traverso M, Accorsi P, Beccaria F, Belcastro V, Capovilla G, Cappanera S, Coppola A, Dalla Bernardina B, Darra F, Ferretti M, Elia M, Galeone D, Giordano L, Gobbi G, Nicita F, Parisi P, Pezzella M, Spalice A, Striano S, Tozzi E, Vignoli A, Minetti C, Zara F, Striano P, Verrotti A. (2013) Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. Eur J Neurol 20:856859.
  • Arsov T, Mullen SA, Damiano JA, Lawrence KM, Huh LL, Nolan M, Young H, Thouin A, Dahl HH, Berkovic SF, Crompton DE, Sadleir LG, Scheffer IE. (2012) Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency. Epilepsia 53:e204e207.
  • Asadi-Pooya A, Emami M, Nikseresht A. (2012) Early-onset versus typical absence epilepsy; clinical and electrographic characteristics. Seizure 21:273275.
  • Caraballo RH, Darra F, Fontana E, Garcia R, Monese E, Dalla Bernardina B. (2011) Absence seizures in the first years of life: an electroclinical study of 46 cases. Epilepsia 52:393400.
  • Cavazzuti GB, Ferrari F, Galli V, Benatti A. (1989) Epilepsy with typical absence seizures with onset during the first year of life. Epilepsia 30:802806.
  • De Marco P. (1980) Petit mal epilepsy during early infancy. Clin Electroencephalogr 11:3840.
  • Farooque P, Goraya J, Valencia I, Carvalho KS, Hardison HH, Legido A, Khurana DS. (2011) Early-onset childhood absence epilepsy: is it a distinct entity? Epileptic Disord 13:411416.
  • Giordano L, Vignoli A, Accorsi P, Galli J, Pezzella M, Traverso M, Battaglia S, Baglietto MG, Beccaria F, Cerminara C, Gambara S, Del Giudice E, Crichiutti G, Bisulli F, Pinci M, Tinuper P, Briatore E, Calzolari S, Coppola A, Canevini MP, Capovilla G, Striano S, Zara F, Minetti C, Striano P. (2011) A clinical and genetic study of 33 new cases with early-onset absence epilepsy. Epilepsy Res 95:221226.
  • Guerrini R, Sanchez-Carpintero R, Deonna T, Santucci M, Bhatia KP, Moreno T, Parmeggiani L, Bernardina BD. (2002) Early-onset absence epilepsy and paroxysmal dyskinesia. Epilepsia 43:12241229.
  • Kobayashi Y, Akasaka N, Ohashi T, Saitoh S, Tomonoh Y, Hirose S, Tohyama J. (2011) Early-onset absence epilepsy at eight months of age. Epileptic Disord 13:417421.
  • Muhle H, Steinich I, Von Spiczak S, Franke A, Weber Y, Lerche H, Wittig M, Heidemann S, Suls A, De Jonghe P, Marini C, Guerrini R, Scheffer IE, Berkovic SF, Stephani U, Siebert R, Sander T, Helbig I, Tönnies H. (2010) A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy. Epilepsia 51:24532456.
  • Panayiotopoulos CP. (2008) Typical absence seizures and related epileptic syndromes: assessment of current state and directions for future research. Epilepsia 49:21312139.
  • Shahar E, Genizi J, Nevo Y, Kaufman R, Cabot S, Zelnik N. (2007) Typical absence epilepsy presenting prior to age of 3 years: an uncommon form of idiopathic generalized epilepsy. Eur J Paediatr Neurol 11:346352.
  • Striano P, Weber YG, Toliat MR, Schubert J, Leu C, Chaimana R, Baulac S, Guerrero R, LeGuern E, Lehesjoki AE, Polvi A, Robbiano A, Serratosa JM, Guerrini R, Nürnberg P, Sander T, Zara F, Lerche H, Marini C, EPICURE Consortium. (2012) GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy. Neurology 78:557562.
  • Suls A, Mullen SA, Weber YG, Verhaert K, Ceulemans B, Guerrini R, Wuttke TV, Salvo-Vargas A, Deprez L, Claes LR, Jordanova A, Berkovic SF, Lerche H, De Jonghe P, Scheffer IE. (2009) Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1. Ann Neurol 66:415419.
  • Verrotti A, Olivieri C, Agostinelli S, Coppola G, Parisi P, Grosso S, Spalice A, Zamponi N, Franzoni E, Iannetti P, Chiarelli F, Curatolo P. (2011) Long term outcome in children affected by absence epilepsy with onset before the age of three years. Epilepsy Behav 20:366369.
  • Verrotti A, Striano P, Agostinelli S. (2013) Early onset absence epilepsy: What changes using Panayiotopoulos’s criteria? Epilepsia 54:765766.