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Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
Gallo V, Dotta L, Giardino G, Cirillo E, Lougaris V, D'Assante R, Prandini A, Consolini R, Farrow EG, Thiffault I, Saunders CJ, Leonardi A, Plebani A, Badolato R, Pignata C. Gallo V, et al. Front Immunol. 2016 Nov 7;7:466. doi: 10.3389/fimmu.2016.00466. eCollection 2016. Front Immunol. 2016. PMID: 27872624 Free PMC article.
Unbalanced Immune System: Immunodeficiencies and Autoimmunity.
Giardino G, Gallo V, Prencipe R, Gaudino G, Romano R, De Cataldis M, Lorello P, Palamaro L, Di Giacomo C, Capalbo D, Cirillo E, D'Assante R, Pignata C. Giardino G, et al. Among authors: gallo v. Front Pediatr. 2016 Oct 6;4:107. doi: 10.3389/fped.2016.00107. eCollection 2016. Front Pediatr. 2016. PMID: 27766253 Free PMC article. Review.
Severe combined immunodeficiences: new and old scenarios.
Aloj G, Giardino G, Valentino L, Maio F, Gallo V, Esposito T, Naddei R, Cirillo E, Pignata C. Aloj G, et al. Among authors: gallo v. Int Rev Immunol. 2012 Feb;31(1):43-65. doi: 10.3109/08830185.2011.644607. Int Rev Immunol. 2012. PMID: 22251007 Review.
FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program.
Romano R, Palamaro L, Fusco A, Giardino G, Gallo V, Del Vecchio L, Pignata C. Romano R, et al. Among authors: gallo v. Front Immunol. 2013 Jul 12;4:187. doi: 10.3389/fimmu.2013.00187. eCollection 2013. Front Immunol. 2013. PMID: 23874334 Free PMC article.
Severe combined immunodeficiency--an update.
Cirillo E, Giardino G, Gallo V, D'Assante R, Grasso F, Romano R, Di Lillo C, Galasso G, Pignata C. Cirillo E, et al. Among authors: gallo v. Ann N Y Acad Sci. 2015 Nov;1356:90-106. doi: 10.1111/nyas.12849. Epub 2015 Jul 31. Ann N Y Acad Sci. 2015. PMID: 26235889 Review.
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis.
Giardino G, Gallo V, Somma D, Farrow EG, Thiffault I, D'Assante R, Donofrio V, Paciolla M, Ursini MV, Leonardi A, Saunders CJ, Pignata C. Giardino G, et al. Among authors: gallo v. J Allergy Clin Immunol. 2016 May;137(5):1591-1595.e4. doi: 10.1016/j.jaci.2015.09.050. Epub 2015 Nov 26. J Allergy Clin Immunol. 2016. PMID: 26632527 No abstract available.
A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome.
Romano R, Cirillo E, Giardino G, Gallo V, Mollica C, Pignata C. Romano R, et al. Among authors: gallo v. J Investig Allergol Clin Immunol. 2016;26(6):390-392. doi: 10.18176/jiaci.0107. J Investig Allergol Clin Immunol. 2016. PMID: 27996952 Free article. No abstract available.
678 results