Abnormal Phonologic Processing in Familial Lateral Temporal Lobe Epilepsy Due to a New LGI1 Mutation
スポンサーリンク
概要
- 論文の詳細を見る
- 2005-01-01
著者
-
MARINI Carla
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
Marini Carla
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
-
Guerrini Renzo
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
-
Guerrini Renzo
Epilepsy Neurophysiology And Neurogenetics Unit Division Of Child Neurology And Psychiatry Universit
-
Guerrini Renzo
Epilepsy Neurophysiology And Neurogenetics Unit Irccs Stella Maris Foundation
-
PISANO Tiziana
Department of Child Neurology and Psychiatry, University of Cagliari
-
BROVEDANI Paola
Neuropsychology Unit, IRCCS Stella Maris Foundation
-
BRIZZOLARA Daniela
Neuropsychology Unit, IRCCS Stella Maris Foundation
-
PRUNA Dario
Department of Child Neurology and Psychiatry, University of Cagliari
-
MEI Davide
Epilepsy, Neurophysiology, and Neurogenetics Unit, IRCCS Stella Maris Foundation
-
MORO Francesca
Epilepsy, Neurophysiology, and Neurogenetics Unit, IRCCS Stella Maris Foundation
-
CIANCHETTI Carlo
Department of Child Neurology and Psychiatry, University of Cagliari
-
Pruna Dario
Department Of Child Neurology And Psychiatry University Of Cagliari
-
Buti Daniela
Neurology And Neurophysiology Unit Department Of Pediatrics University Of Florence Azienda Ospedalie
-
Moro Francesca
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
-
Pisano Tiziana
Department Of Child Neurology And Psychiatry University Of Cagliari
-
Mei Davide
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
-
Cianchetti Carlo
Department Of Child Neurology And Psychiatry University Of Cagliari
-
Brovedani Paola
Neuropsychology Unit Irccs Stella Maris Foundation
-
Guerrini Renzo
Neurosciences Unit Institute Of Child Health And Great Ormond Street Hospital For Children Universit
関連論文
- Genetic Architecture of Idiopathic Generalized Epilepsy : Clinical Genetic Analysis of 55 Multiplex Families
- No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
- EEG in Adult-onset Idiopathic Generalized Epilepsy
- Abnormal Phonologic Processing in Familial Lateral Temporal Lobe Epilepsy Due to a New LGI1 Mutation
- Generalized Epilepsy with Febrile Seizures Plus (GEFS^+) : Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
- Adolescent Onset of Idiopathic Photosensitive Occipital Epilepsy After Remission of Benign Rolandic Epilepsy
- Delayed appearance of interictal EEG abnormalities in early onset childhood epilepsy with occipital paroxysms
- Genetic Malformations of the Cerebral Cortex and Epilepsy
- Physiology of Human Photosensitivity
- Epileptic Syndromes and Visually Induced Seizures
- Different Neurophysiologic Patterns of Myoclonus Characterize Lennox-Gastaut Syndrome and Myoclonic Astatic Epilepsy
- Epilepsy in Offspring of Whom Both Parents Have Idiopathic Generalized Epilepsy : Biparental Inheritance