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Fetal acetylcholine receptor inactivation syndrome: A myopathy due to maternal antibodies.
Hacohen Y, Jacobson LW, Byrne S, Norwood F, Lall A, Robb S, Dilena R, Fumagalli M, Born AP, Clarke D, Lim M, Vincent A, Jungbluth H. Hacohen Y, et al. Among authors: fumagalli m. Neurol Neuroimmunol Neuroinflamm. 2014 Dec 23;2(1):e57. doi: 10.1212/NXI.0000000000000057. eCollection 2015 Feb. Neurol Neuroimmunol Neuroinflamm. 2014. PMID: 25566546 Free PMC article.
Survival rate and neurodevelopmental outcome of extremely premature babies: an 8-year experience of an Italian single neonatal tertiary care center.
Uccella S, De Carli A, Sirgiovanni I, Schiavolin P, Damiano G, Ghirardi B, Maglioli Carpano F, Bassi L, Gangi S, Picciolini O, Fumagalli M, Mosca F. Uccella S, et al. Among authors: fumagalli m. Pediatr Med Chir. 2015 Dec 29;37(3):pmc.2015.106. doi: 10.4081/pmc.2015.106. Pediatr Med Chir. 2015. PMID: 26714779 Free article.
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy.
Dilena R, DiFrancesco JC, Soldovieri MV, Giacobbe A, Ambrosino P, Mosca I, Galli MA, Guez S, Fumagalli M, Miceli F, Cattaneo D, Darra F, Gennaro E, Zara F, Striano P, Castellotti B, Gellera C, Varesio C, Veggiotti P, Taglialatela M. Dilena R, et al. Among authors: fumagalli m. Neurotherapeutics. 2018 Oct;15(4):1112-1126. doi: 10.1007/s13311-018-0657-9. Neurotherapeutics. 2018. PMID: 30112700 Free PMC article.
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
Villa R, Fergnani VGC, Silipigni R, Guerneri S, Cinnante C, Guala A, Danesino C, Scola E, Conte G, Fumagalli M, Gangi S, Colombo L, Picciolini O, Ajmone PF, Accogli A, Madia F, Tassano E, Scala M, Capra V, Srour M, Spaccini L, Righini A, Greco D, Castiglia L, Romano C, Bedeschi MF. Villa R, et al. Among authors: fumagalli m. Eur J Paediatr Neurol. 2020 Sep;28:110-119. doi: 10.1016/j.ejpn.2020.07.002. Epub 2020 Jul 28. Eur J Paediatr Neurol. 2020. PMID: 32800423 Free article.
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates.
Dilena R, Raviglione F, Cantalupo G, Cordelli DM, De Liso P, Di Capua M, Falsaperla R, Ferrari F, Fumagalli M, Lori S, Suppiej A, Tadini L, Dalla Bernardina B, Mastrangelo M, Pisani F; INNESCO Group. Dilena R, et al. Among authors: fumagalli m. Clin Neurophysiol. 2021 Apr;132(4):886-903. doi: 10.1016/j.clinph.2021.01.012. Epub 2021 Feb 3. Clin Neurophysiol. 2021. PMID: 33684728 Free article.
A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome.
Fumagalli M, Ronchi D, Bedeschi MF, Manini A, Cristofori G, Mosca F, Dilena R, Sciacco M, Zanotti S, Piga D, Ardissino G, Triulzi F, Corti S, Comi GP, Salviati L. Fumagalli M, et al. Mol Genet Metab Rep. 2022 Jun 18;32:100887. doi: 10.1016/j.ymgmr.2022.100887. eCollection 2022 Sep. Mol Genet Metab Rep. 2022. PMID: 35756861 Free PMC article.
618 results