Adolescent Onset of Idiopathic Photosensitive Occipital Epilepsy After Remission of Benign Rolandic Epilepsy
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概要
- 論文の詳細を見る
- 1997-07-01
著者
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GUERRINI Renzo
Institute of Child Neurology, Psychiatry and Educational Psychology, University of Pisa and Research
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BONANNI Paolo
Institute of Child Neurology, Psychiatry and Educational Psychology, University of Pisa and Research
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BELMONTE Anna
Institute of Child Neurology and Psychiatry, University of Pisa
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Belmonte Anna
Institute Of Child Neurology And Psychiatry University Of Pisa
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Belmonte Anna
Institute Of Child Neurology And Psychiatry University Of Pisa Irccs `stella Maris'foundation
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Guerrini Renzo
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
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Guerrini Renzo
Epilepsy Neurophysiology And Neurogenetics Unit Irccs Stella Maris Foundation
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Bonanni Paolo
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
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Bonanni Paolo
Institute Of Child Neurology Psychiatry And Educational Psychology University Of Pisa And Research I
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Parmeggiani Lucio
Neurosciences Unit Institute Of Child Health And Great Ormond Street Hospital For Children Universit
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Parmeggiani Lucio
Institute Of Child Neurology And Psychiatry Univertsity Of Pisa And Institute For Clinical Research
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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Guerrini Renzo
Neurosciences Unit Institute Of Child Health And Great Ormond Street Hospital For Children Universit
関連論文
- Familial Epilepsy with Unilateral and Bilateral Malformations of Cortical Development
- Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy
- Idiopathic Photosensitive Occipital Lobe Epilepsy
- No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
- Panic Attacks Mistaken for Relapse of 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
- Myoclonic Absence-Like Seizures and Chromosome Abnormality Syndromes
- 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
- Reversible Pseudoatrophy of the Brain and Mental Deterioration Associated with Valproate Treatment
- Antiepileptic Drug-Induced Worsening of Seizures in Children
- Paroxysmal tonic upgaze of childhood with ataxia: a benign transient dystonia with autosomal dominant inheritance
- Are there generalised spike waves and typical absences in benign rolandic epilepsy?
- Myoclonic status epilepticus following high-dosage lamotrigine therapy
- A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
- Physiology of Human Photosensitivity
- Continuous Spike-and-Wave Activity During Slow-Wave Sleep : Syndrome or EEG Pattern?
- Different Neurophysiologic Patterns of Myoclonus Characterize Lennox-Gastaut Syndrome and Myoclonic Astatic Epilepsy