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Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome.
Buijsse, Nathan; Jansen, Floor E; Ockeloen, Charlotte W; van Kempen, Marjan J A; Zeidler, Shimriet; Willemsen, Marjolein H; Scarano, Emanuela; Monticone, Sonia; Zonneveld-Huijssoon, Evelien; Low, Karen J; Bayat, Allan; Sisodiya, Sanjay M; Samanta, Debopam; Lesca, Gaetan; de Jong, Danielle; Giltay, Jaqcues C; Verbeek, Nienke E; Kleefstra, Tjitske; Brilstra, Eva H; Vlaskamp, Danique R M.
Afiliación
  • Buijsse N; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Jansen FE; Department of Pediatric Neurology, Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Ockeloen CW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Kempen MJA; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Zeidler S; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Willemsen MH; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Scarano E; Department of Pediatrics, St. Orsola-Malpighi Hospital, Bologna, Italy.
  • Monticone S; Department of Pediatrics, Azienda Ospedaliero Universitaria Maggiore della Carità, Novara, Italy.
  • Zonneveld-Huijssoon E; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Low KJ; Department of Clinical Genetics, University Hospitals Bristol and Weston NHS trust, University of Bristol, Bristol, UK.
  • Bayat A; Department for Genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark.
  • Sisodiya SM; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Samanta D; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology and Chalfont Centre for Epilepsy, Chalfont St Peter, UK.
  • Lesca G; Child Neurology Section, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • de Jong D; Department of Genetics, University Hospitals of Lyon, Lyon, France.
  • Giltay JC; Department of Neurology, Academic Center for Epileptology Kempenhaeghe/MUMC+, Heeze, The Netherlands.
  • Verbeek NE; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Kleefstra T; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Brilstra EH; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Vlaskamp DRM; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
Epilepsia Open ; 8(4): 1300-1313, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37501353
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Dentarias / Anomalías Múltiples / Enfermedades del Desarrollo Óseo / Epilepsia Generalizada / Discapacidad Intelectual Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans / Infant Idioma: En Revista: Epilepsia Open Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Dentarias / Anomalías Múltiples / Enfermedades del Desarrollo Óseo / Epilepsia Generalizada / Discapacidad Intelectual Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans / Infant Idioma: En Revista: Epilepsia Open Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Estados Unidos