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作者:Luke D. Kartsounis , Rajith de Silva
来源:[J].Cortex(IF 6.161), 2010, Vol.47 (4), pp.451-459
摘要:Abstract(#br)We describe the case of a patient with confirmed voltage-gated potassium channel antibody-associated encephalitis (VGKC-Ab). MRI studies revealed bilateral hyper-intensity in the hippocampi, with their volumes preserved. At presentation, the patient's anterograde and...
作者:Luke D. Kartsounis , Svetislav Gacinovic ...
来源:[J].Journal of Neurology(IF 3.578), 2004, Vol.251 (1), pp.91-98
摘要:Abstract. (#br)Hyperekplexia (HE), or startle disease, is usually afamilial disorder associated with mutations in the glycinereceptor α1 subunit gene ( GLRA1 ), characterised by exaggeratedstartle reactions to unexpected auditory, somaesthetic andvisual stimuli. Non-familial...
作者:Luke D. Kartsounis , Dominic G. O’Donovan ...
来源:[J].Archives of Neurology(IF 7.584), 2010, Vol.67 (11), pp.1399-1402
摘要:BACKGROUND Mitochondrial diseases are characterized by wide phenotypic and genetic variability, but presentations in adults with akinetic rigidity and hyperkinetic movement disorders are rare. OBJECTIVES To describe clinically a subject with progressive neurodegeneration characte...

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