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机译:癫痫和癫痫发作在22Q11.2删除综合征:患病率和与其他神经发育障碍的联系
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
The Epilepsy UnitUniversity Hospital of WalesCardiff UK;
Betsi Cadwaladr University Health BoardWales UK;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
School of Physiology Pharmacology and NeuroscienceUniversity of BristolBristol UK;
Immunodeficiency Centre for WalesUniversity Hospital of WalesCardiff UK;
Medical Research Council Centre for Neuropsychiatric Genetics and GenomicsCardiff University School;
electroencephalography; febrile seizure; psychiatric disorder; seizure semiology; unprovoked seizure;
机译:癫痫和癫痫发作在22Q11.2删除综合征:患病率和与其他神经发育障碍的联系
机译:22Q11.2删除综合征降低成人患者的癫痫发作阈值,没有癫痫
机译:22q11.2删除综合征中的全身性癫痫和肌阵挛性发作
机译:22Q11.2缺失综合征在调查白质改变的替代扩散各向异性措施
机译:时间加工和神经发育障碍:从注意力缺陷/多动障碍,自闭症谱系障碍和22q11.2删除综合征的见解。
机译:患有22q11.2缺失综合征的年轻人的癫痫和癫痫发作的患病率及其与其他神经发育障碍的联系
机译:22Q11.2缺失综合征中的广义癫痫和肌阵挛性癫痫发作