A New Chrna4 Mutation with Low Penetrance in Nocturnal Frontal Lobe Epilepsy
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概要
- 論文の詳細を見る
- 2003-07-01
著者
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Steinlein Ortrud
Institute Of Human Genetics University Hospital Bonn
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Steinlein Ortrud
Institut Fur Humangenetik Rheinische Friendrich-wilhelms-universitat
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Bertrand Daniel
Department Of Physiology Cmu
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Hufnagel Andreas
Department Of Epileptology University Of Bonn
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LENIGER Tobias
Department of Neurology, University of Essen
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KANANURA Colette
Institute of Human Genetics, University Hospital Bonn
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BERTRAND Sonia
Department of Physiology, CMU
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Bertrand Sonia
Department Of Physiology Cmu
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Leniger Tobias
Department Of Neurology University Of Essen Essen
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Leniger Tobias
Department Of Neurology Department Of Psychiatry And Psychotherapy University Of Essen
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Kananura Colette
Institute Of Human Genetics University Hospital Bonn
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- Surgical Treatment of Extratemporal Epilepsy: Clinical, Radiologic, and Histopathologic Findings in 60 Patients
- Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
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- The relevance of interictal rCBF brain SPECT in temporal lobe epilepsy: Diagnostical value and effects of spatial resolution
- Seizure-Associated Headache in Epilepsy
- A New Chrna4 Mutation with Low Penetrance in Nocturnal Frontal Lobe Epilepsy
- Carbonic Anhydrase Inhibitor Sulthiame Reduces Intracellular pH and Epileptiform Activity of Hippocampal CA3 Neurons
- Autosomal Dominant Nocturnal Frontal Lobe Epilepsy : An Electroclinical Study of a Norwegian Family with Ten Affected Members
- Familial Temporal Lobe Epilepsy with Aphasic Seizures and Linkage to Chromosome 10q22-q24
- Speech-induced Aphasic Seizures in Epilepsy Caused by LGI1 Mutation
- Asymmetry of Long-latency Auditory Evoked Potentials in LGI1-related Autosomal Dominant Lateral Temporal Lobe Epilepsy
- Idiopathic Epilepsies with a Monogenic Mode of Inheritance