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119 results

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Page 1
The phenotypic spectrum of epilepsy associated with periventricular nodular heterotopia.
Paliotti K, Dassi C, Berrahmoune S, Bejaran ML, Davila CEV, Martinez AB, Estupiñà MCF, Mancardi MM, Riva A, Giacomini T, Severino M, Romaniello R, Dubeau F, Srour M, Myers KA. Paliotti K, et al. Among authors: mancardi mm. J Neurol. 2023 Aug;270(8):3934-3945. doi: 10.1007/s00415-023-11724-z. Epub 2023 Apr 29. J Neurol. 2023. PMID: 37119372
Type 1 diabetes and epilepsy: more than a casual association?
Mancardi MM, Striano P, Giannattasio A, Baglietto MG, Errichiello L, Zara F, Prato G, Minuto N, Veneselli E, Lorini R, D'Annunzio G. Mancardi MM, et al. Epilepsia. 2010 Feb;51(2):320-1. doi: 10.1111/j.1528-1167.2009.02380.x. Epilepsia. 2010. PMID: 20331700 Free article. No abstract available.
Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.
Michelucci R, Scudellaro E, Testoni S, Passarelli D, Riguzzi P, Diani E, Vazza G, Vianello V, Scabar A, Mostacciuolo ML, Volpi L, Rubboli G, Pinardi F, Mancardi MM, Tassinari CA, Nobile C. Michelucci R, et al. Among authors: mancardi mm. Epilepsy Res. 2008 Jul;80(1):9-17. doi: 10.1016/j.eplepsyres.2008.03.014. Epub 2008 May 27. Epilepsy Res. 2008. PMID: 18508238
Guidelines for Vascular Anomalies by the Italian Society for the study of Vascular Anomalies (SISAV).
Stillo F, Mattassi R, Diociaiuti A, Neri I, Baraldini V, Dalmonte P, Amato B, Ametrano O, Amico G, Bianchini G, Campisi C, Cattaneo E, Causin F, Cavalli R, Colletti G, Corbeddu M, Coppo P, DE Fiores A, DI Giuseppe P, El Hachem M, Esposito F, Fulcheri E, Gandolfo C, Grussu F, Guglielmo A, Leuzzi M, Manunza F, Moneghini L, Monzani N, Nicodemi E, Occella C, Orso M, Pagella F, Paolantonio G, Pasetti F, Rollo M, Ruggiero F, Santecchia L, Spaccini L, Taurino M, Vaghi M, Vercellio G, Zama M, Zocca A, Aguglia M, Castronovo EL, DE Lorenzi E, Fontana E, Gusson E, Lanza J, Lizzio R, Mancardi MM, Rosina E. Stillo F, et al. Among authors: mancardi mm. Int Angiol. 2022 Apr;41(2 Suppl 1):1-130. doi: 10.23736/S0392-9590.22.04902-1. Int Angiol. 2022. PMID: 35546136 Free article. No abstract available.
Novel CNS malformations and skeletal anomalies in a patient with Beaulieu-boycott-Innes syndrome.
Accogli A, Scala M, Calcagno A, Castello R, Torella A, Musacchia F, Allegri AME, Mancardi MM, Maghnie M, Severino M; Telethon Undiagnosed Diseases Program; Nigro V, Capra V. Accogli A, et al. Among authors: mancardi mm. Am J Med Genet A. 2018 Dec;176(12):2835-2840. doi: 10.1002/ajmg.a.40534. Epub 2018 Sep 20. Am J Med Genet A. 2018. PMID: 30238602 Review.
119 results