Phenotypic traits and family history in patients with 22q11.2 deletion syndrome and generalized epilepsy: A multicenter case-control study.
Cerulli Irelli E, Fanella M, Chaumette B, Putotto C, Mignot C, Mazzeo A, Lemke JR, Riva A, Accinni T, Louveau C, Giovannetti A, Pugnaloni F, Gavaret M, Di Fabio F, Fortunato F, Dorn T, Ferlazzo E, Gambardella A, Ramantani G, Orlando B, Iftimovici A, Operto FF, Pulvirenti F, Kluger G, Caputo V, Striano P, Di Bonaventura C.
Cerulli Irelli E, et al. Among authors: iftimovici a.
Epilepsia. 2024 Dec 24. doi: 10.1111/epi.18220. Online ahead of print.
Epilepsia. 2024.
PMID: 39718534