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A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus.
Maini I, Farnetti E, Caraffi SG, Ivanovski I, De Bernardi ML, Gelmini C, Pollazzon M, Rosato S, Laurie S, Matalonga L, Baldo C, Garavelli L. Maini I, et al. Among authors: farnetti e. Neuropediatrics. 2018 Jun;49(3):222-224. doi: 10.1055/s-0038-1641722. Epub 2018 Apr 11. Neuropediatrics. 2018. PMID: 29642246 No abstract available.
VEXAS Syndrome: A Case Series From a Single-Center Cohort of Italian Patients With Vasculitis.
Muratore F, Marvisi C, Castrignanò P, Nicoli D, Farnetti E, Bonanno O, Longo R, Zaldini P, Galli E, Balanda N, Beck DB, Grayson PC, Pipitone N, Boiardi L, Salvarani C. Muratore F, et al. Among authors: farnetti e. Arthritis Rheumatol. 2022 Apr;74(4):665-670. doi: 10.1002/art.41992. Epub 2022 Mar 3. Arthritis Rheumatol. 2022. PMID: 34611997 Free PMC article.
Peptide Receptor Radionuclide Therapy-Induced Gitelman-like Syndrome.
Negro A, Rossi GM, Nicoli D, Versari A, Farnetti E, Santi R, De Pietri S. Negro A, et al. Among authors: farnetti e. Am J Kidney Dis. 2017 Nov;70(5):725-728. doi: 10.1053/j.ajkd.2017.05.024. Epub 2017 Jul 21. Am J Kidney Dis. 2017. PMID: 28739329
Intercellular adhesion molecule-1 gene polymorphisms in Behçet's Disease.
Boiardi L, Salvarani C, Casali B, Olivieri I, Ciancio G, Cantini F, Salvi F, Malatesta R, Govoni M, Trotta F, Filippini D, Paolazzi G, Nicoli D, Farnetti E, Macchioni L. Boiardi L, et al. Among authors: farnetti e. J Rheumatol. 2001 Jun;28(6):1283-7. J Rheumatol. 2001. PMID: 11409120
Endothelial nitric oxide synthase gene polymorphisms in Behçet's disease.
Salvarani C, Boiardi L, Casali B, Olivieri I, Ciancio G, Cantini F, Salvi F, Malatesta R, Govoni M, Trotta F, Filippini D, Paolazzi G, Nicoli D, Farnetti E, Macchioni P. Salvarani C, et al. Among authors: farnetti e. J Rheumatol. 2002 Mar;29(3):535-40. J Rheumatol. 2002. PMID: 11908569
63 results