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Page 1
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.
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.
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.
Cirillo E, Giardino G, Gallo V, Puliafito P, Azzari C, Bacchetta R, Cardinale F, Cicalese MP, Consolini R, Martino S, Martire B, Molinatto C, Plebani A, Scarano G, Soresina A, Cancrini C, Rossi P, Digilio MC, Pignata C. Cirillo E, et al. Among authors: gallo v. BMC Med Genet. 2014 Jan 2;15:1. doi: 10.1186/1471-2350-15-1. BMC Med Genet. 2014. PMID: 24383682 Free PMC article.
677 results