Epilesies with single gene inheritance
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概要
著者
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Berkovic Samuel
Department Of Neurology University Of Melbourne Austin Hospital
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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
Department Of Medicine (neurology) University Of Melbourne Austin & Repatriation Medical Centre
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Berkovic Samuel
Department Of Medicine (neurology) The University Of Melbourne
-
Berkovic Samuel
Department Of Medicine (neurology) Austin And Repatriation Medical Centre University Of Melbourne
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Berkovic Samuel
Department Of Medicine (neurology) University Of Melbourne Austin & Repatriation Medical Centre
関連論文
- Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
- 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
- Genetic Architecture of Idiopathic Generalized Epilepsy : Clinical Genetic Analysis of 55 Multiplex Families
- Prolactin Levels in Sudden Unexpected Death in Epilepsy
- Chromosomal Abnormalities and Epilepsy : A Review for Clinicians and Gene Hunters
- Temporal Lobe Epilepsy Subtypes: Differential Patterns of Cerebral Perfusion on Ictal SPECT
- 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
- Epilesies with single gene inheritance
- Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
- 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