Attività di ricerca
Ultime pubblicazioni:
-
Johnson, J.O., Chia, R., Miller, D.E., Li, R., Kumaran, R., Abramzon, Y., et al. (2021). Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis. JAMA NEUROLOGY, 78(10), 1236-1248 [10.1001/jamaneurol.2021.2598]. - dettaglio
-
Ricci, C., Cerase, A., Riolo, G., Manasse, G., & Battistini, S. (2021). KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants. JOURNAL OF MOLECULAR NEUROSCIENCE, 71(9), 1876-1883 [10.1007/s12031-021-01814-w]. - dettaglio
-
Riolo, G., Ricci, C., & Battistini, S. (2021). Molecular genetic features of cerebral cavernous malformations (CCM) patients: An overall view from genes to endothelial cells. CELLS, 10(3), 1-19 [10.3390/cells10030704]. - dettaglio
-
Ricci, C., Riolo, G., & Battistini, S. (2021). Molecular genetic analysis of cerebral cavernous malformations: An update. VESSEL PLUS, 5, 1-14 [10.20517/2574-1209.2021.28]. - dettaglio
-
Ricci, C., Giannini, F., Riolo, G., Bocci, S., Casali, S., & Battistini, S. (2021). A novel variant in superoxide dismutase 1 gene (P.V119M) in als patients with pure lower motor neuron presentation. GENES, 12(10), 1-10 [10.3390/genes12101544]. - dettaglio
