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Intracranial pressure monitoring in patients with acute brain injury in the intensive care unit (SYNAPSE-ICU): an international, prospective observational cohort study.
Robba C, Graziano F, Rebora P, Elli F, Giussani C, Oddo M, Meyfroidt G, Helbok R, Taccone FS, Prisco L, Vincent JL, Suarez JI, Stocchetti N, Citerio G; SYNAPSE-ICU Investigators. Robba C, et al. Among authors: elli f. Lancet Neurol. 2021 Jul;20(7):548-558. doi: 10.1016/S1474-4422(21)00138-1. Lancet Neurol. 2021. PMID: 34146513 Free article.
Comparison of multiple definitions for ventilator-associated pneumonia in patients requiring mechanical ventilation for non-pulmonary conditions: preliminary data from PULMIVAP, an Italian multi-centre cohort study.
Alagna L, Palomba E, Chatenoud L, Massafra R, Magni F, Mancabelli L, Donnini S, Elli F, Forastieri A, Gaipa G, Abbruzzese C, Fumagalli R, Munari M, Panacea A, Picetti E, Terranova L, Turroni F, Vaschetto R, Zoerle T, Citerio G, Gori A, Bandera A. Alagna L, et al. Among authors: elli f. J Hosp Infect. 2023 Oct;140:90-95. doi: 10.1016/j.jhin.2023.07.023. Epub 2023 Aug 9. J Hosp Infect. 2023. PMID: 37562590 Free article.
MesenchymAl stromal cells for Traumatic bRain Injury (MATRIx): a study protocol for a multicenter, double-blind, randomised, placebo-controlled phase II trial.
Zanier ER, Pischiutta F, Rulli E, Vargiolu A, Elli F, Gritti P, Gaipa G, Belotti D, Basso G, Zoerle T, Stocchetti N, Citerio G; MATRIx Study group. Zanier ER, et al. Among authors: elli f. Intensive Care Med Exp. 2023 Aug 25;11(1):56. doi: 10.1186/s40635-023-00535-1. Intensive Care Med Exp. 2023. PMID: 37620640 Free PMC article.
Analysis of genetic variants of phosphodiesterase 11A in acromegalic patients.
Peverelli E, Ermetici F, Filopanti M, Elli FM, Ronchi CL, Mantovani G, Ferrero S, Bosari S, Beck-Peccoz P, Lania A, Spada A. Peverelli E, et al. Among authors: elli fm. Eur J Endocrinol. 2009 Nov;161(5):687-94. doi: 10.1530/EJE-09-0677. Epub 2009 Aug 11. Eur J Endocrinol. 2009. PMID: 19671705
Pseudohypoparathyroidism and GNAS epigenetic defects: clinical evaluation of albright hereditary osteodystrophy and molecular analysis in 40 patients.
Mantovani G, de Sanctis L, Barbieri AM, Elli FM, Bollati V, Vaira V, Labarile P, Bondioni S, Peverelli E, Lania AG, Beck-Peccoz P, Spada A. Mantovani G, et al. J Clin Endocrinol Metab. 2010 Feb;95(2):651-8. doi: 10.1210/jc.2009-0176. Epub 2010 Jan 8. J Clin Endocrinol Metab. 2010. PMID: 20061437 Free article.
84 results