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Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group.
Klepper J, Akman C, Armeno M, Auvin S, Cervenka M, Cross HJ, De Giorgis V, Della Marina A, Engelstad K, Heussinger N, Kossoff EH, Leen WG, Leiendecker B, Monani UR, Oguni H, Neal E, Pascual JM, Pearson TS, Pons R, Scheffer IE, Veggiotti P, Willemsen M, Zuberi SM, De Vivo DC. Klepper J, et al. Among authors: de vivo dc, de giorgis v. Epilepsia Open. 2020 Aug 13;5(3):354-365. doi: 10.1002/epi4.12414. eCollection 2020 Sep. Epilepsia Open. 2020. PMID: 32913944 Free PMC article.
Mitochondrial Disease.
Pons R, De Vivo DC. Pons R, et al. Among authors: de vivo dc. Curr Treat Options Neurol. 2001 May;3(3):271-288. doi: 10.1007/s11940-001-0008-7. Curr Treat Options Neurol. 2001. PMID: 11282042
EEG features of glut-1 deficiency syndrome.
von Moers A, Brockmann K, Wang D, Korenke CG, Huppke P, De Vivo DC, Hanefeld F. von Moers A, et al. Among authors: de vivo dc. Epilepsia. 2002 Aug;43(8):941-5. doi: 10.1046/j.1528-1157.2002.50401.x. Epilepsia. 2002. PMID: 12181017 Free article.
Glucose transporter protein syndromes.
De Vivo DC, Wang D, Pascual JM, Ho YY. De Vivo DC, et al. Int Rev Neurobiol. 2002;51:259-88. doi: 10.1016/s0074-7742(02)51008-4. Int Rev Neurobiol. 2002. PMID: 12420362 Review. No abstract available.
Mitochondrial DNA abnormalities and autistic spectrum disorders.
Pons R, Andreu AL, Checcarelli N, Vilà MR, Engelstad K, Sue CM, Shungu D, Haggerty R, de Vivo DC, DiMauro S. Pons R, et al. Among authors: de vivo dc. J Pediatr. 2004 Jan;144(1):81-5. doi: 10.1016/j.jpeds.2003.10.023. J Pediatr. 2004. PMID: 14722523
GLUT1 deficiency and other glucose transporter diseases.
Pascual JM, Wang D, Lecumberri B, Yang H, Mao X, Yang R, De Vivo DC. Pascual JM, et al. Among authors: de vivo dc. Eur J Endocrinol. 2004 May;150(5):627-33. doi: 10.1530/eje.0.1500627. Eur J Endocrinol. 2004. PMID: 15132717 Review.
354 results