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Page 1
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P; Italian Network for Primary Immunodeficiencies. Cancrini C, et al. J Pediatr. 2014 Jun;164(6):1475-80.e2. doi: 10.1016/j.jpeds.2014.01.056. Epub 2014 Mar 20. J Pediatr. 2014. PMID: 24657119
Corrigendum to: "Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET)" [Vaccine 36 (2018) Pages 3541-3542].
Martire B, Azzari C, Badolato R, Canessa C, Cirillo E, Gallo V, Graziani S, Lorenzini T, Milito C, Panza R, Moschese V; with Italian Network for Primary Immunodeficiencies (IPINET). Martire B, et al. Vaccine. 2018 Nov 29;36(50):7753. doi: 10.1016/j.vaccine.2018.10.056. Epub 2018 Oct 30. Vaccine. 2018. PMID: 30389193 No abstract available.
The quality of life of children and adolescents with X-linked agammaglobulinemia.
Soresina A, Nacinovich R, Bomba M, Cassani M, Molinaro A, Sciotto A, Martino S, Cardinale F, De Mattia D, Putti C, Dellepiane RM, Felici L, Parrinello G, Neri F, Plebani A; Italian Network for Primary Immunodeficiencies. Soresina A, et al. J Clin Immunol. 2009 Jul;29(4):501-7. doi: 10.1007/s10875-008-9270-8. Epub 2008 Dec 17. J Clin Immunol. 2009. PMID: 19089603
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.
Lorenzini T, Giacomelli M, Scomodon O, Cortesi M, Rivellini V, Dotta L, Soresina A, Dellepiane RM, Carrabba M, Cossu F, Cancrini C, Specchia F, Giardino G, Pignata C, Plebani A, Pietrogrande MC, Badolato R; IPINET (Italian Network for Primary Immunodeficiencies). Lorenzini T, et al. J Allergy Clin Immunol Pract. 2019 Jul-Aug;7(6):2072-2075.e4. doi: 10.1016/j.jaip.2019.02.012. Epub 2019 Feb 20. J Allergy Clin Immunol Pract. 2019. PMID: 30797078 No abstract available.
Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: an Italian multicenter study.
Di Matteo G, Giordani L, Finocchi A, Ventura A, Chiriaco M, Blancato J, Sinibaldi C, Plebani A, Soresina A, Pignata C, Dellepiane RM, Trizzino A, Cossu F, Rondelli R, Rossi P, De Mattia D, Martire B; IPINET (Italian Network for Primary Immunodeficiencies). Di Matteo G, et al. Mol Immunol. 2009 Jun;46(10):1935-41. doi: 10.1016/j.molimm.2009.03.016. Epub 2009 May 1. Mol Immunol. 2009. PMID: 19410294