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Paroxysmal events in glucose transporter type 1 deficiency syndrome : Early identification of their true nature is important

ContributorsKorff, Christianorcid
Published inDevelopmental medicine and child neurology, vol. 66, no. 11, p. 1403-1404
Publication date2024-11
First online date2024-06-17
Abstract

Commentary on : Ito Y, Nakatsukasa H, Toyoma Y, Nagata S, Oguni H. Differentiating non-epileptic seizures from epileptic seizures in Glut1 deficiency syndrome. Dev Med Child Neurol. 2024 Nov;66(11):1466-1475. doi: 10.1111/dmcn.15942. Epub 2024 Apr 24. PMID: 38655597.

Keywords
  • Humans
  • Infant
  • Male
  • Carbohydrate Metabolism, Inborn Errors / diagnosis
  • Carbohydrate Metabolism, Inborn Errors / genetics
  • Carbohydrate Metabolism, Inborn Errors / physiopathology
  • Monosaccharide Transport Proteins / deficiency
  • Monosaccharide Transport Proteins / genetics
Citation (ISO format)
KORFF, Christian. Paroxysmal events in glucose transporter type 1 deficiency syndrome : Early identification of their true nature is important. In: Developmental medicine and child neurology, 2024, vol. 66, n° 11, p. 1403–1404. doi: 10.1111/dmcn.16000
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Journal ISSN0012-1622
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Creation19/08/2025 07:50:02
First validation06/10/2025 09:49:50
Update24/03/2026 09:04:44
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