Teaching activities
Course year: 1
First cycle degree (DM 270)
DIETISTIC
A.Y. 2025/2026
Course year: 1
First cycle degree (DM 270)
Dental Hygiene
A.Y. 2025/2026
Research
Ultime pubblicazioni:
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Daga, S., Loberti, L., Rollo, G., Adamo, L., Colavecchio, O.L., Brunelli, G., et al. (2025). Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant. EUROPEAN JOURNAL OF HUMAN GENETICS, 33(4), 461-467 [10.1038/s41431-024-01706-8]. - view more
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Minnai, F., Biscarini, F., Esposito, M., Dragani, T.A., Bujanda, L., Rahmouni, S., et al. (2024). A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death. SCIENTIFIC REPORTS, 14(1) [10.1038/s41598-024-53310-x]. - view more
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Serio, V.B., Palmieri, M., Innamorato, S., Loberti, L., Fallerini, C., Ariani, F., et al. (2023). Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors. FRONTIERS IN GENETICS, 14 [10.3389/fgene.2023.1213283]. - view more
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Bergantini, L., Baldassarri, M., D’Alessandro, M., Brunelli, G., Fabbri, G., Zguro, K., et al. (2023). Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder. RESPIRATORY RESEARCH, 24(1), 1-9 [10.1186/s12931-023-02458-7]. - view more
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Doddato, G., Fabbiani, A., Fallerini, C., Bruttini, M., Hadjistilianou, T., Landi, M., et al. (2023). Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype. FRONTIERS IN GENETICS, 14 [10.3389/fgene.2023.1143795]. - view more
