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579 results

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Page 1
Myoclonus: Differential diagnosis and current management.
Riva A, D'Onofrio G, Ferlazzo E, Pascarella A, Pasini E, Franceschetti S, Panzica F, Canafoglia L, Vignoli A, Coppola A, Badioni V, Beccaria F, Labate A, Gambardella A, Romeo A, Capovilla G, Michelucci R, Striano P, Belcastro V. Riva A, et al. Epilepsia Open. 2024 Apr;9(2):486-500. doi: 10.1002/epi4.12917. Epub 2024 Feb 9. Epilepsia Open. 2024. PMID: 38334331 Free PMC article. Review.
Current and promising therapeutic options for Dravet syndrome.
Riva A, D'Onofrio G, Amadori E, Tripodi D, Balagura G, Iurilli V, Vari MS, Verrotti A, Striano P. Riva A, et al. Expert Opin Pharmacother. 2022 Oct;23(15):1727-1736. doi: 10.1080/14656566.2022.2127089. Epub 2022 Sep 21. Expert Opin Pharmacother. 2022. PMID: 36124778 Review.
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. 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.
Expanding the phenotype associated with biallelic SLC20A2 variants.
D'Onofrio G, Scala M, Severino M, Roberti R, Romano F, De Marco P, Iacomino M, Baldassari S, Uva P, Pavanello M, Gustincich S, Striano P, Zara F, Capra V. D'Onofrio G, et al. Eur J Hum Genet. 2023 Jul;31(7):725-729. doi: 10.1038/s41431-023-01349-1. Epub 2023 Mar 28. Eur J Hum Genet. 2023. PMID: 36977836 Free PMC article. No abstract available.
Novel biallelic variants expand the phenotype of NAA20-related syndrome.
D'Onofrio G, Cuccurullo C, Larsen SK, Severino M, D'Amico A, Brønstad K, AlOwain M, Morrison JL, Wheeler PG, Webb BD, Alfalah A, Iacomino M, Uva P, Coppola A, Merla G, Salpietro VD, Zara F, Striano P, Accogli A, Arnesen T, Bilo L. D'Onofrio G, et al. Clin Genet. 2023 Sep;104(3):371-376. doi: 10.1111/cge.14359. Epub 2023 May 16. Clin Genet. 2023. PMID: 37191084
579 results