Familial Epilepsy with Unilateral and Bilateral Malformations of Cortical Development
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概要
- 論文の詳細を見る
- 1999-01-01
著者
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DRAVET Charlotte
Centre Saint-Paul
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GUERRINI Renzo
Institute of Child Neurology, Psychiatry and Educational Psychology, University of Pisa and Research
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Dravet Charlotte
Centre Saint-paul For Epilepsy
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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BARTOLOMEI Fabrice
Centre Saint Paul
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GAVARET Martine
Centre Saint-Paul for Epilepsy
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Dravet Charlotte
Centre Saint Paul
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Bartolomei Fabrice
Centre Saint-paul For Epilepsy
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GUERRINI Renzo
Institute of Child Neurology and Psychiatry, University of Pisa
関連論文
- Abnormal Neuroimaging in Patients with Benign Epilepsy with Centrotemporal Spikes
- Clinical Research : Incidence of Drug-Induced Aggravation in Benign Epilepsy with Centrotemporal Spikes
- Severe Myoclonic Epilepsy in Infants and its Related Syndromes
- Severe myoclonic epilepsy in infants and its related syndromes
- Familial Epilepsy with Unilateral and Bilateral Malformations of Cortical Development
- Severe myoclonic epilepsy in infants and its related syndromes
- Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy
- Idiopathic Photosensitive Occipital Lobe Epilepsy
- Panic Attacks Mistaken for Relapse of Epilepsy
- 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
- Continuous Spike-and-Wave Activity During Slow-Wave Sleep : Syndrome or EEG Pattern?