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A real-life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy.
Riva A, Roberti R, D'Onofrio G, Vari MS, Amadori E, De Giorgis V, Cerminara C, Specchio N, Pietrafusa N, Tombini M, Assenza G, Cappanera S, Marini C, Rasmini P, Veggiotti P, Zara F, Russo E, Striano P. Riva A, et al. Among authors: de giorgis v. Epilepsia Open. 2023 Sep;8(3):1142-1150. doi: 10.1002/epi4.12717. Epub 2023 May 15. Epilepsia Open. 2023. PMID: 36840436 Free PMC article.
Triheptanoin Did Not Show Benefit versus Placebo for the Treatment of Paroxysmal Movement Disorders in Glut1 Deficiency Syndrome: Results of a Randomized Phase 3 Study.
De Giorgis V, Bhatia KP, Boespflug-Tanguy O, Gras D, Marina AD, Desurkar A, Toledo M, Miller I, Rotstein M, Schneider SA, Tarquinio DC, Weber Y, Brandabur M, Mayhew J, Koutsoukos T, De Vivo DC. De Giorgis V, et al. Among authors: de vivo dc. Mov Disord. 2024 Aug;39(8):1386-1396. doi: 10.1002/mds.29822. Epub 2024 May 9. Mov Disord. 2024. PMID: 38725190 Clinical Trial.
Sporadic and familial glut1ds Italian patients: A wide clinical variability.
De Giorgis V, Teutonico F, Cereda C, Balottin U, Bianchi M, Giordano L, Olivotto S, Ragona F, Tagliabue A, Zorzi G, Nardocci N, Veggiotti P. De Giorgis V, et al. Seizure. 2015 Jan;24:28-32. doi: 10.1016/j.seizure.2014.11.009. Epub 2014 Nov 26. Seizure. 2015. PMID: 25564316 Free article.
Atypical Manifestations in Glut1 Deficiency Syndrome.
De Giorgis V, Varesio C, Baldassari C, Piazza E, Olivotto S, Macasaet J, Balottin U, Veggiotti P. De Giorgis V, et al. J Child Neurol. 2016 Aug;31(9):1174-80. doi: 10.1177/0883073816650033. Epub 2016 Jun 1. J Child Neurol. 2016. PMID: 27250207
The changing face of dietary therapy for epilepsy.
Pasca L, De Giorgis V, Macasaet JA, Trentani C, Tagliabue A, Veggiotti P. Pasca L, et al. Among authors: de giorgis v. Eur J Pediatr. 2016 Oct;175(10):1267-76. doi: 10.1007/s00431-016-2765-z. Epub 2016 Sep 1. Eur J Pediatr. 2016. PMID: 27586246 Review.
115 results