A clinical and genetic study of 33 new cases with early-onset absence epilepsy

[1]  J. Klepper.  GLUT1 deficiency syndrome in clinical practice , 2012, Epilepsy Research.

[2]  E. Ishii,et al.  Atypical childhood absence epilepsy with preceding or simultaneous generalized tonic clonic seizures , 2011, Brain and Development.

[3]  S. Byrne,et al.  Refractory absence epilepsy associated with GLUT‐1 deficiency syndrome , 2011, Epilepsia.

[4]  E. Ishii,et al.  Idiopathic childhood occipital epilepsy of Gastaut: report of 12 patients. , 2011, Pediatric neurology.

[5]  P. Curatolo,et al.  Long term outcome in children affected by absence epilepsy with onset before the age of three years , 2011, Epilepsy & Behavior.

[6]  B. dalla Bernardina,et al.  Absence seizures in the first 3 years of life: An electroclinical study of 46 cases , 2011, Epilepsia.

[7]  I. Scheffer,et al.  Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency , 2010, Neurology.

[8]  David C. Reutens,et al.  Atlas of epilepsies , 2010 .

[9]  E. Hirsch,et al.  Other Probable Syndromes of Idiopathic Generalized Epilepsies , 2010 .

[10]  I. Scheffer,et al.  Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1 , 2009, Annals of neurology.

[11]  P. Striano,et al.  Comment on “Factors influencing clinical features of absence seizures” , 2009, Epilepsia.

[12]  Laurel A. Slaughter,et al.  New GLUT-1 mutation in a child with treatment-resistant epilepsy , 2009, Epilepsy Research.

[13]  J. Carlin,et al.  Factors influencing clinical features of absence seizures , 2008, Epilepsia.

[14]  M. Maeder-Ingvar,et al.  Glut‐1 deficiency syndrome masquerading
 as idiopathic generalized epilepsy , 2008, Epilepsia.

[15]  W. van Paesschen,et al.  Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 , 2008, Brain : a journal of neurology.

[16]  Timothy A. Pedley,et al.  Epilepsy : a comprehensive textbook , 2008 .

[17]  E. Shahar,et al.  Typical absence epilepsy presenting prior to age of 3 years: an uncommon form of idiopathic generalized epilepsy. , 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[18]  I. Maestro,et al.  Early-onset absence epilepsy: Clinical and electroencephalographic features in three children , 2006, Brain and Development.

[19]  C. Panayiotopoulos.  Syndromes of Idiopathic Generalized Epilepsies Not Recognized by the International League Against Epilepsy , 2005, Epilepsia.

[20]  Paolo Balestri,et al.  Childhood Absence Epilepsy: Evolution and Prognostic Factors , 2005, Epilepsia.

[21]  Mark Gardiner,et al.  Genetics of Idiopathic Generalized Epilepsies , 2005, Epilepsia.

[22]  D. Nordli,et al.  Idiopathic Generalized Epilepsies Recognized by the International League Against Epilepsy , 2005, Epilepsia.

[23]  J. Roger,et al.  Epileptic Syndromes in Infancy, Childhood and Adolescence , 2005 .

[24]  E. K. Louis,et al.  Pattern‐sensitive Epilepsy: Electroclinical Characteristics, Natural History, and Delineation of the Epileptic Syndrome , 2005, Epilepsia.

[25]  H. Doose.  Absence epilepsy of early childhood —genetic aspects , 1994, European Journal of Pediatrics.

[26]  V. Laguitton,et al.  Absence Epilepsy with Onset before Age Three Years: A Heterogeneous and Often Severe Condition , 2003, Epilepsia.

[27]  C. Chi,et al.  Childhood absence epilepsy. , 1994, Zhonghua yi xue za zhi = Chinese medical journal; Free China ed.

[28]  R J Porter,et al.  The Absence Epilepsies , 1993, Epilepsia.

[29]  F. Ferrari,et al.  Epilepsy with Typical Absence Seizures with Onset During the First Year of Life , 1989, Epilepsia.

[30]  R. Mattson,et al.  Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy. , 1989, Epilepsia.