Genetic Association Studies in Epilepsy : "The Truth Is Out There"
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概要
- 論文の詳細を見る
- 2004-11-01
著者
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Berkovic Samuel
University Of Melbourne Austin And Repatriation Medical Centre
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Berkovic Samuel
Epilepsy Research Institute
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Berkovic Samuel
Epilepsy Research Centre And Department Of Medicine (neurology) University Of Melbourne
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Mulley John
Women's And Children's Hospital
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Mulley John
Department Of Genetic Medicine Women's And Children's Hospital And Department Of Molecular
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Mulley John
Department Of Cytogenetics And Molecular Genetics Centre For Medical Genetics Women's And Child
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TAN Nigel
Epilepsy Research Centre and Department of Medicine (Neurology), University of Melbourne
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Tan Nigel
Epilepsy Research Centre And Department Of Medicine (neurology) University Of Melbourne
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Mulley John
Department Of Genetic Medicine Women's And Children's Hospital And Department Of Molecular
関連論文
- Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)
- Familial Partial Epilepsy with Variable Foci : Clinical Features and Linkage to Chromosome 22q12
- Genetic Architecture of Idiopathic Generalized Epilepsy : Clinical Genetic Analysis of 55 Multiplex Families
- Is Variation in the GABA(B) Receptor 1 Gene Associated with Temporal Lobe Epilepsy?
- Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
- Chromosomal Abnormalities and Epilepsy : A Review for Clinicians and Gene Hunters
- The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
- EEG in Adult-onset Idiopathic Generalized Epilepsy
- II D1 EEG in adult-onset idiopathic generalized epilepsy
- Benign Partial Seizures of Adolescence
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
- Idiopathic Generalized Epilepsies : Do Sporadic and Familial Cases Deffer?
- Epilepsy in Offspring of Whom Both Parents Have Idiopathic Generalized Epilepsy : Biparental Inheritance
- Febrile Convulsions and Genetic Susceptibility : Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit
- Genetics of the Epilepsies
- S1-2 Molecular genetics of epilepsies : Impact on clinical care and understanding neurobiology(The 40th Congress of the Japan Epilepsy Society)
- Hypothalamic Hamartoma and Seizures : A Treatable Epileptic Encephalopathy
- S4-1 Overview on genetics of epilepsy including perspectives in epilepsy research