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Identification of a Novel Mutation in TNFAIP3 in a Family With Poly-Autoimmunity.
Rossi MN, Federici S, Uva A, Passarelli C, Celani C, Caiello I, Matteo V, Petrocchi S, Mortari EP, De Benedetti F, Prencipe G, Insalaco A. Rossi MN, et al. Among authors: passarelli c. Front Immunol. 2022 Jan 26;13:804401. doi: 10.3389/fimmu.2022.804401. eCollection 2022. Front Immunol. 2022. PMID: 35154120 Free PMC article.
ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study.
Caorsi R, Penco F, Grossi A, Insalaco A, Omenetti A, Alessio M, Conti G, Marchetti F, Picco P, Tommasini A, Martino S, Malattia C, Gallizzi R, Podda RA, Salis A, Falcini F, Schena F, Garbarino F, Morreale A, Pardeo M, Ventrici C, Passarelli C, Zhou Q, Severino M, Gandolfo C, Damonte G, Martini A, Ravelli A, Aksentijevich I, Ceccherini I, Gattorno M. Caorsi R, et al. Among authors: passarelli c. Ann Rheum Dis. 2017 Oct;76(10):1648-1656. doi: 10.1136/annrheumdis-2016-210802. Epub 2017 May 18. Ann Rheum Dis. 2017. PMID: 28522451 Free article.
Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome.
Volpi S, Insalaco A, Caorsi R, Santori E, Messia V, Sacco O, Terheggen-Lagro S, Cardinale F, Scarselli A, Pastorino C, Moneta G, Cangemi G, Passarelli C, Ricci M, Girosi D, Derchi M, Bocca P, Diociaiuti A, El Hachem M, Cancrini C, Tomà P, Granata C, Ravelli A, Candotti F, Picco P, DeBenedetti F, Gattorno M. Volpi S, et al. Among authors: passarelli c. J Clin Immunol. 2019 Jul;39(5):476-485. doi: 10.1007/s10875-019-00645-0. Epub 2019 May 29. J Clin Immunol. 2019. PMID: 31144250 Free PMC article.
Early Treatment and IL1RN Single-Nucleotide Polymorphisms Affect Response to Anakinra in Systemic Juvenile Idiopathic Arthritis.
Pardeo M, Rossi MN, Pires Marafon D, Sacco E, Bracaglia C, Passarelli C, Caiello I, Marucci G, Insalaco A, Perrone C, Tulone A, Prencipe G, De Benedetti F. Pardeo M, et al. Among authors: passarelli c. Arthritis Rheumatol. 2021 Jun;73(6):1053-1061. doi: 10.1002/art.41612. Epub 2021 May 2. Arthritis Rheumatol. 2021. PMID: 33615724
Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals.
Maltese PE, Colombo L, Martella S, Rossetti L, El Shamieh S, Sinibaldi L, Passarelli C, Coppè AM, Buzzonetti L, Falsini B, Chiurazzi P, Placidi G, Tanzi B, Bertelli M, Iarossi G. Maltese PE, et al. Among authors: passarelli c. Front Genet. 2022 Jun 28;13:914345. doi: 10.3389/fgene.2022.914345. eCollection 2022. Front Genet. 2022. PMID: 35836572 Free PMC article.
A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients.
Iarossi G, Sinibaldi L, Passarelli C, Coppe' AM, Cappelli A, Petrocelli G, Catena G, Perrone C, Falsini B, Novelli A, Bartuli A, Buzzonetti L. Iarossi G, et al. Among authors: passarelli c. Diagnostics (Basel). 2022 Sep 9;12(9):2183. doi: 10.3390/diagnostics12092183. Diagnostics (Basel). 2022. PMID: 36140584 Free PMC article.
75 results