المؤلفون: van Gemert LA; Department of Pediatric Neurology, Amalia Children's Hospital, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525, GA, Nijmegen, the Netherlands. Electronic address: loes.vangemert@radboudumc.nl., Leen WG; Department of Neurology, Canisius Wilhelmina Hospital, Weg Door Jonkerbos 100, 6532, SZ, Nijmegen, the Netherlands. Electronic address: w.leen@cwz.nl., Draaisma JM; Department of General Pediatrics, Amalia Children's Hospital, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525, GA, Nijmegen, the Netherlands. Electronic address: jos.draaisma@radboudumc.nl., Roeleveld N; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525, GA, Nijmegen, the Netherlands. Electronic address: nel.roeleveld@radboudumc.nl., Willemsen MA; Department of Pediatric Neurology, Amalia Children's Hospital, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525, GA, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Montessorilaan 3, 6525, HR, Nijmegen, the Netherlands. Electronic address: Michel.willemsen@radboudumc.nl.

المصدر: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society [Eur J Paediatr Neurol] 2022 May; Vol. 38, pp. 73-76. Date of Electronic Publication: 2022 Apr 27.

نوع المنشور: Journal Article; Observational Study

بيانات الدورية: Publisher: Saunders Country of Publication: England NLM ID: 9715169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2130 (Electronic) Linking ISSN: 10903798 NLM ISO Abbreviation: Eur J Paediatr Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Carbohydrate Metabolism, Inborn Errors* , Diet, Ketogenic* , Microcephaly*/complications , Microcephaly*/epidemiology, Glucose Transporter Type 1/*metabolism, Glucose Transporter Type 1/genetics ; Humans ; Monosaccharide Transport Proteins/deficiency

SCR Disease Name: Glut1 Deficiency Syndrome