Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.

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Title: Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.
Authors: Eaton CB; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; Cerebra Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Birmingham, UK., Thomas RH; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; Institute of Neuroscience, Newcastle University, Newcastle-upon-Tyne, UK., Hamandi K; The Epilepsy Unit, University Hospital of Wales, Cardiff, UK., Payne GC; Betsi Cadwaladr University Health Board, Wales, UK., Kerr MP; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK., Linden DEJ; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands., Owen MJ; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK., Cunningham AC; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK., Bartsch U; School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.; Lilly UK Erl Wood Manor, Surrey, UK., Struik SS; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK., van den Bree MBM; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
Source: Epilepsia [Epilepsia] 2019 May; Vol. 60 (5), pp. 818-829. Date of Electronic Publication: 2019 Apr 11.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE
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  Data: Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.
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  Data: <searchLink fieldCode="AU" term="%22Eaton+CB%22">Eaton CB</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; Cerebra Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22Thomas+RH%22">Thomas RH</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; Institute of Neuroscience, Newcastle University, Newcastle-upon-Tyne, UK.<br /><searchLink fieldCode="AU" term="%22Hamandi+K%22">Hamandi K</searchLink>; The Epilepsy Unit, University Hospital of Wales, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22Payne+GC%22">Payne GC</searchLink>; Betsi Cadwaladr University Health Board, Wales, UK.<br /><searchLink fieldCode="AU" term="%22Kerr+MP%22">Kerr MP</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22Linden+DEJ%22">Linden DEJ</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.; School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Owen+MJ%22">Owen MJ</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22Cunningham+AC%22">Cunningham AC</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22Bartsch+U%22">Bartsch U</searchLink>; School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.; Lilly UK Erl Wood Manor, Surrey, UK.<br /><searchLink fieldCode="AU" term="%22Struik+SS%22">Struik SS</searchLink>; Immunodeficiency Centre for Wales, University Hospital of Wales, Cardiff, UK.<br /><searchLink fieldCode="AU" term="%22van+den+Bree+MBM%22">van den Bree MBM</searchLink>; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
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  Data: <searchLink fieldCode="JN" term="%222983306R%22">Epilepsia</searchLink> [Epilepsia] 2019 May; Vol. 60 (5), pp. 818-829. <i>Date of Electronic Publication: </i>2019 Apr 11.
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