Chromosomal Abnormalities and Epilepsy : A Review for Clinicians and Gene Hunters
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概要
- 論文の詳細を見る
- 2002-02-01
著者
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Berkovic Samuel
University Of Melbourne Austin And Repatriation Medical Centre
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Berkovic Samuel
Epilepsy Research Centre And Department Of Medicine (neurology) University Of Melbourne
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Berkovic Samuel
Department Of Neurology University Of Melbourne Austin Hospital
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CROSSLAND Kathryn
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
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Scheffer Ingrid
University Of Melbourne Austin And Repatriation Medical Centre
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Scheffer Ingrid
Department Of Medicine The University Of Melbourne Austin Health
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Scheffer Ingrid
Department Of Medicine (neurology) Royal Children's Hospital And Monash Medical Centre Austin A
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Scheffer Ingrid
Austin Hospital University Of Melbourne
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SINGH Rita
Department of Medicine (Neurology), The University of Melbourne
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GARDNER R.
Murdoch Children's Research Institute, Royal Children's Hospital
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CROSSLAND Kathryn
Department of Medicine (Neurology), The University of Melbourne
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Crossland Kathryn
Department Of Medicine (neurology) The University Of Melbourne
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Singh Rita
Department Of Medicine (neurology) The University Of Melbourne
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Scheffer Ingrid
Department Of Medicine (neurology) The University Of Melbourne
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Berkovic Samuel
Department Of Medicine (neurology) The University Of Melbourne
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Berkovic Samuel
Department Of Medicine (neurology) Austin And Repatriation Medical Centre University Of Melbourne
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Gardner R.
Murdoch Children's Research Institute Royal Children's Hospital
関連論文
- Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
- Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)
- Subtle Microscopic Abnormalities in Hippocampal Sclerosis Do Not Predict Clinical Features of Temporal Lobe Epilepsy
- Hemicranial Volume Deficits in Patients with Temporal Lobe Epilepsy With and Without Hippocampal Sclerosis
- 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
- Prolactin Levels in Sudden Unexpected Death in Epilepsy
- 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
- Temporal Lobe Epilepsy Subtypes: Differential Patterns of Cerebral Perfusion on Ictal SPECT
- Reflex Seizures in Patients with Malformations of Cortical Development and Refractory Epilepsy
- EEG in Adult-onset Idiopathic Generalized Epilepsy
- II D1 EEG in adult-onset idiopathic generalized epilepsy
- Benign Partial Seizures of Adolescence
- Ictal SPECT and Interictal PET in the Localization of Occipital Lobe Epilepsy
- Idiopathic Generalized Epilepsy with Generalized and Other Seizures in Adolescence
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
- Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus
- Epilesies with single gene inheritance
- Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
- Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
- Idiopathic Generalized Epilepsies : Do Sporadic and Familial Cases Deffer?
- Epilepsy in Offspring of Whom Both Parents Have Idiopathic Generalized Epilepsy : Biparental Inheritance
- 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
- Human Epileptogenesis and Hypothalamic Hamartomas: New Lessons from an Experiment of Nature
- Epilepsy Genes and the Genetics of Epilepsy Syndromes: The Promise of New Therapies Based on Genetic Knowledge
- Aggravation of Generalized Epilepsies
- Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX