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Page 1
From Genetic Testing to Precision Medicine in Epilepsy.
Striano P, Minassian BA. Striano P, et al. Among authors: minassian ba. Neurotherapeutics. 2020 Apr;17(2):609-615. doi: 10.1007/s13311-020-00835-4. Neurotherapeutics. 2020. PMID: 31981099 Free PMC article. Review.
Clinical and genetic findings in 26 Italian patients with Lafora disease.
Franceschetti S, Gambardella A, Canafoglia L, Striano P, Lohi H, Gennaro E, Ianzano L, Veggiotti P, Sofia V, Biondi R, Striano S, Gellera C, Annesi G, Madia F, Civitelli D, Rocca FE, Quattrone A, Avanzini G, Minassian B, Zara F. Franceschetti S, et al. Epilepsia. 2006 Mar;47(3):640-3. doi: 10.1111/j.1528-1167.2006.00479.x. Epilepsia. 2006. PMID: 16529633 Free article.
Typical progression of myoclonic epilepsy of the Lafora type: a case report.
Striano P, Zara F, Turnbull J, Girard JM, Ackerley CA, Cervasio M, De Rosa G, Del Basso-De Caro ML, Striano S, Minassian BA. Striano P, et al. Among authors: minassian ba. Nat Clin Pract Neurol. 2008 Feb;4(2):106-11. doi: 10.1038/ncpneuro0706. Nat Clin Pract Neurol. 2008. PMID: 18256682
22-year-old girl with status epilepticus and progressive neurological symptoms.
Striano P, Ackerley CA, Cervasio M, Girard JM, Turnbull J, Del Basso-De Caro ML, Striano S, Zara F, Minassian BA. Striano P, et al. Among authors: minassian ba. Brain Pathol. 2009 Oct;19(4):727-30. doi: 10.1111/j.1750-3639.2009.00308.x. Brain Pathol. 2009. PMID: 19744044 Free PMC article.
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy.
de Lange IM, Helbig KL, Weckhuysen S, Møller RS, Velinov M, Dolzhanskaya N, Marsh E, Helbig I, Devinsky O, Tang S, Mefford HC, Myers CT, van Paesschen W, Striano P, van Gassen K, van Kempen M, de Kovel CG, Piard J, Minassian BA, Nezarati MM, Pessoa A, Jacquette A, Maher B, Balestrini S, Sisodiya S, Warde MT, De St Martin A, Chelly J; EuroEPINOMICS-RES MAE working group; van 't Slot R, Van Maldergem L, Brilstra EH, Koeleman BP. de Lange IM, et al. Among authors: minassian ba. J Med Genet. 2016 Dec;53(12):850-858. doi: 10.1136/jmedgenet-2016-103909. Epub 2016 Jun 29. J Med Genet. 2016. PMID: 27358180 Free PMC article.
The history of progressive myoclonus epilepsies.
Genton P, Striano P, Minassian BA. Genton P, et al. Among authors: minassian ba. Epileptic Disord. 2016 Sep 1;18(S2):3-10. doi: 10.1684/epd.2016.0834. Epileptic Disord. 2016. PMID: 27621064 Free PMC article. Review.
Progressive Myoclonus Epilepsy: The Gene-Empowered Era.
Minassian BA, Striano P, Avanzini G. Minassian BA, et al. Epileptic Disord. 2016 Sep 1;18(S2):1-2. doi: 10.1684/epd.2016.0864. Epileptic Disord. 2016. PMID: 27694067 Free PMC article. No abstract available.
Lafora disease.
Turnbull J, Tiberia E, Striano P, Genton P, Carpenter S, Ackerley CA, Minassian BA. Turnbull J, et al. Among authors: minassian ba. Epileptic Disord. 2016 Sep 1;18(S2):38-62. doi: 10.1684/epd.2016.0842. Epileptic Disord. 2016. PMID: 27702709 Free PMC article. Review.
222 results