Genetic Architecture of Idiopathic Generalized Epilepsy : Clinical Genetic Analysis of 55 Multiplex Families
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-05-01
著者
-
Berkovic Samuel
University Of Melbourne Austin And Repatriation Medical Centre
-
Berkovic Samuel
Epilepsy Research Institute
-
Berkovic Samuel
Epilepsy Research Centre And Department Of Medicine (neurology) University Of Melbourne
-
Neufeld Miriam
Department Of Neurology Tel-aviv Sourasky Medical Center
-
Neufeld Miriam
Department Of Neurology Elias Sourasky Medical Center Tel-aviv University
-
Mulley John
Women's And Children's Hospital
-
Mulley John
Department Of Genetic Medicine Women's And Children's Hospital And Department Of Molecular
-
Wallace Robyn
Centre For Medical Genetics Department Of Laboratory Genetics Women's And Children's Hospi
-
SCHEFFER Ingrid
Epilepsy Research Centre, University of Melbourne, Austin & Repatriation Medical Centre
-
MULLEY John
Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women's and Children
-
MARINI Carla
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
CROSSLAND Kathryn
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
GRINTON Bronwyn
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
PHILLIPS Fiona
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
MCMAHON Jacinta
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
TURNER Samantha
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
DEAN Joanne
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
-
KIVITY Sara
Department of Neurology, Schneider Children's Medical Center
-
MAZARIB Aziz
Department of Neurology, Tel-Aviv Sourasky Medical Center
-
KORCZYN Amos
Sieratzki Chair of Neurology, Tel Aviv University
-
HARKIN Louise
Centre for Medical Genetics, Department of Laboratory Genetics, Women's and Children's Hospital
-
DIBBENS Leanne
Centre for Medical Genetics, Department of Laboratory Genetics, Women's and Children's Hospital
-
Kivity Sara
Department Of Neurology Schneider Children's Medical Center
-
Marini Carla
Epilepsy Neurophysiology Neurogenetics Unit Irccs Fondazione Stella Maris
-
Mazarib Aziz
Department Of Neurology Tel-aviv Sourasky Medical Center
-
Korczyn Amos
Sieratzki Chair Of Neurology Tel Aviv University
-
Harkin Louise
Centre For Medical Genetics Department Of Laboratory Genetics Women's And Children's Hospi
-
Dibbens Leanne
Centre For Medical Genetics Department Of Laboratory Genetics Women's And Children's Hospi
-
Phillips Fiona
Epilepsy Research Institute Department Of Medicine (neurology) The University Of Melbourne
-
Dean Joanne
Epilepsy Research Institute Department Of Medicine (neurology) The University Of Melbourne
-
Mcmahon Jacinta
Epilepsy Research Institute Department Of Medicine (neurology) The University Of Melbourne
-
Turner Samantha
Epilepsy Research Institute Department Of Medicine (neurology) The University Of Melbourne
-
Grinton Bronwyn
Epilepsy Research Institute Department Of Medicine (neurology) The University Of Melbourne
-
Scheffer Ingrid
University Of Melbourne Austin And Repatriation Medical Centre
-
Scheffer Ingrid
Austin Hospital University Of Melbourne
-
Crossland Kathryn
Department Of Medicine (neurology) The University Of Melbourne
-
Scheffer Ingrid
Department Of Medicine (neurology) The University Of Melbourne
-
Berkovic Samuel
Department Of Medicine (neurology) The University Of Melbourne
-
Mulley John
Department Of Genetic Medicine Women's And Children's Hospital And Department Of Molecular
-
SCHEFFER Ingrid
Epilepsy Research Centre and Department of Medicine (Neurology), University of Melbourne
関連論文
- 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
- 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
- Ictal SPECT and Interictal PET in the Localization of Occipital Lobe Epilepsy
- Abnormal Phonologic Processing in Familial Lateral Temporal Lobe Epilepsy Due to a New LGI1 Mutation
- Generalized Epilepsy with Febrile Seizures Plus (GEFS^+) : Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
- Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus
- Epilesies with single gene inheritance
- 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
- 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
- Self-Efficacy and Social Support as Mediators in the Relation Between Disease Severity and Quality of Life in Patients with Epilepsy