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From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
Hully M, Vuillaumier-Barrot S, Le Bizec C, Boddaert N, Kaminska A, Lascelles K, de Lonlay P, Cances C, des Portes V, Roubertie A, Doummar D, LeBihannic A, Degos B, de Saint Martin A, Flori E, Pedespan JM, Goldenberg A, Vanhulle C, Bekri S, Roubergue A, Heron B, Cournelle MA, Kuster A, Chenouard A, Loiseau MN, Valayannopoulos V, Chemaly N, Gitiaux C, Seta N, Bahi-Buisson N. Hully M, et al. Among authors: chenouard a. Eur J Med Genet. 2015 Sep;58(9):443-54. doi: 10.1016/j.ejmg.2015.06.007. Epub 2015 Jul 17. Eur J Med Genet. 2015. PMID: 26193382
A Cause of Permanent Ketosis: GLUT-1 Deficiency.
Chenouard A, Vuillaumier-Barrot S, Seta N, Kuster A. Chenouard A, et al. JIMD Rep. 2015;18:79-83. doi: 10.1007/8904_2014_352. Epub 2014 Sep 26. JIMD Rep. 2015. PMID: 25256448 Free PMC article.
Interrater Agreement Between Critical Care Providers for Background Classification and Seizure Detection After Implementation of Amplitude-Integrated Electroencephalography in Neonates, Infants, and Children.
Bourgoin P, Barrault V, Loron G, Roger A, Bataille E, Leclair-Visonneau L, Joram N, Chenouard A. Bourgoin P, et al. Among authors: chenouard a. J Clin Neurophysiol. 2020 May;37(3):259-262. doi: 10.1097/WNP.0000000000000634. J Clin Neurophysiol. 2020. PMID: 31567529
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