Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy
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概要
- 論文の詳細を見る
- 1998-05-01
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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GENTON Pierre
Centre Saint Paul
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DULAC Olivier
Neuropediatric Department, Hospital Saint Vincent de Paul
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Dulac Olivier
Neuropediatric Department Hospital Saint Vincent De Paul
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Dulac Olivier
Neuropediatrie Hopital Saint-vincent-de Paul
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Kaminska Anna
Neuropediatrie Hopital Saint-vincent-de Paul
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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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Dravet Charlotte
Centre Saint Paul Marseille
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Guerrini Renzo
Ipe University Of Pisa.irccs Stella Maris
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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Dravet Charlotte
Centre Saint Paul
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GENTON Pierre
Centre Saint Paul-H.
関連論文
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- 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
- Is Refractory Epilepsy Preventable?
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- Panic Attacks Mistaken for Relapse of Epilepsy
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- Adolescent Onset of Idiopathic Photosensitive Occipital Epilepsy After Remission of Benign Rolandic Epilepsy
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- Reversible Pseudoatrophy of the Brain and Mental Deterioration Associated with Valproate Treatment
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- Worsening of Seizures by Oxcarbazepine in Juvenile Idiopathic Generalized Epilepsies
- Response : Benign Epilepsy of Childhood with Malformations of Cortical Development BECTS and Neuroradiology
- Are there generalised spike waves and typical absences in benign rolandic epilepsy?
- Benign Childhood Epilepsy with Centrotemporal Spikes and Hippocampal Atrophy
- Antimyoclonic Effect of Levetiracetam in 13 Patients with Unverricht-Lundborg Disease : Clinical Observations
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- Complete Loss of the Cytoplasmic Carboxyl Terminus of the KCNQ2 Potassium Channel : A Novel Mutation in a Large Czech Pedigree with Benign Neonatal Convulsions or Other Epileptic Phenotypes
- Clinical and Genetic Analysis of a New Multigenerational Pedigree with GEFS^+ (Generalized Epilepsy with Febrile Seizures Plus)
- When antiepilepitic drugs aggravate epilepsy
- Founder Effect in Patients with Unverricht-Lundborg Disease on Reunion Island
- On the Association Between Valproate and Polycystic Ovary Syndrome
- Tiagabine in Clinical Practice
- Is Schizophrenia a Risk Factor for Epilepsy or Acute Symptomatic Seizures?
- Myoclonic status epilepticus following high-dosage lamotrigine therapy
- Carbamazepine Intoxication with Negative Myoclonus After the Addition of Clobazam
- 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?
- Epileptic Syndromes and Visually Induced Seizures
- FIRES : Febrile infection responsive epileptic (FIRE) encephalopathies of school age
- Introduction
- Aggravation of Seizures by Antiepileptic Drugs: What to Do in Clinical Practice
- Worsening of negative myoclonus by lamotrigine in a case of idiopathic focal epilepsy of children with long-term follow-up