Myoclonic Absence-Like Seizures and Chromosome Abnormality Syndromes
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概要
- 論文の詳細を見る
- 1998-06-01
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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Gambardella Antonio
Institute Of Neurology University Magna Graecia Catanzaro
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Musumeci Sebastiano
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs)
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa-irccs Stella Maris Foundation
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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Gambardella Antonio
Institute Of Neurology School Of Medicine University Magna Graecia
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AGUGLIA Umberto
Regional Epilepsy Centre, Hospital of Reggio Calabria
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Aguglia Umberto
Department Of Medical Sciences School Of Medicine University Of Catanzaro
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ELIA Maurizio
Department of Neurology, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS),
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BONANI Paolo
Institute of Child Neurology and Psychiatry, University of Pisa-IRCCS Stella Maris Foundation
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GAMBARDELLA Antonio
Insitute of Neurology, University of Reggio Calabria
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AGUGLIA Umberto
Insitute of Neurology, University of Reggio Calabria
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Bonani Paolo
Institute Of Child Neurology And Psychiatry University Of Pisa-irccs Stella Maris Foundation
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Elia Maurizio
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs) Tr
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Elia Maurizio
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging
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Musumeci Sebastiano
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs) Tr
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Musumeci Sebastiano
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging
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
- Panic Attacks Mistaken for Relapse of Epilepsy
- ApoE Epsilon4 Allele and Disease Duration Affect Verbal Learning in Mild Temporal Lobe Epilepsy
- Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus
- Prodynorphin Gene Promoter Polymorphism and Temporal Lobe Epilepsy
- Apolipoprotein E Polymorphisms and the Risk of Nonlesional Temporal Lobe Epilepsy
- Spontaneous remission of childhood epilepsy in two patients with focal extraopercular cortical dysplasia
- Emotion-Induced Myoclonic Absence-Like Seizures in a Patient with Inv-Dup(15) Syndrome : A Clinical, EEG and Molecular Genetic Study
- Myoclonic Absence-Like Seizures and Chromosome Abnormality Syndromes
- Negative Myoclonic Status Due to Antiepileptic Drug Tapering: Report of Three Cases
- Photic-Induced Epileptic Negative Myoclonus: A Case Report
- Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients
- Startle epilepsy complicating aspartylglucosaminuria
- 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?
- Chromosome Abnormalities and Epilepsy
- Sleep in subjects with autistic disrder : a neurophysiological and psychological study
- Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome
- Trisomy 12p and epilepsy with myoclonic absences
- A further family with epilepsy, dementia and yellow teeth: the Kohlschutter syndrome
- Myoclonic status epilepticus following high-dosage lamotrigine therapy
- Reflex periodic spasms induced by eating
- A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood-onset Cognitive Deficit
- Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilesia partialis continua
- A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
- Mild Generalized Epilepsy and Developmental Disorder Associated with Large Inv Dup(15)
- Continuous Spike-and-Wave Activity During Slow-Wave Sleep : Syndrome or EEG Pattern?
- Sleep disturbances in Angelman syndrome : a questionnaire study
- A t(4;9)(q34;p22) Translocation Associated with Partial Epilepsy, Mental Retardation, and Dysmorphism