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Page 1
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease.
Rigoli L, Romano C, Caruso RA, Lo Presti MA, Di Bella C, Procopio V, Lo Giudice G, Amorini M, Costantino G, Sergi MD, Cuppari C, Calabro GE, Gallizzi R, Salpietro CD, Fries W. Rigoli L, et al. Among authors: gallizzi r. World J Gastroenterol. 2008 Jul 28;14(28):4454-61. doi: 10.3748/wjg.14.4454. World J Gastroenterol. 2008. PMID: 18680223 Free PMC article.
MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement.
Brancati F, Iannicelli M, Travaglini L, Mazzotta A, Bertini E, Boltshauser E, D'Arrigo S, Emma F, Fazzi E, Gallizzi R, Gentile M, Loncarevic D, Mejaski-Bosnjak V, Pantaleoni C, Rigoli L, Salpietro CD, Signorini S, Stringini GR, Verloes A, Zabloka D, Dallapiccola B, Gleeson JG, Valente EM; International JSRD Study Group. Brancati F, et al. Among authors: gallizzi r. Hum Mutat. 2009 Feb;30(2):E432-42. doi: 10.1002/humu.20924. Hum Mutat. 2009. PMID: 19058225 Free PMC article.
Gene-environment interaction in childhood asthma.
Rigoli L, Briuglia S, Caimmi S, Ferraú V, Gallizzi R, Leonardi S, La Rosa M, Salpietro C. Rigoli L, et al. Among authors: gallizzi r. Int J Immunopathol Pharmacol. 2011 Oct;24(4 Suppl):41-7. doi: 10.1177/03946320110240S409. Int J Immunopathol Pharmacol. 2011. PMID: 22032786 Free article. Review.
Subangular mandibular abscess as presentation of Kawasaki Disease.
Alterio T, Gallizzi R, Salpietro V, Cardile S, Centorrino R, Manti S, Chirico V, Ciprandi G, Salpietro C. Alterio T, et al. Among authors: gallizzi r. Indian J Pediatr. 2014 Apr;81(4):418-9. doi: 10.1007/s12098-014-1396-5. Epub 2014 Mar 14. Indian J Pediatr. 2014. PMID: 24623097 No abstract available.
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
Autoimmune liver disease in Noonan Syndrome.
Loddo I, Romano C, Cutrupi MC, Sciveres M, Riva S, Salpietro A, Ferraù V, Gallizzi R, Briuglia S. Loddo I, et al. Among authors: gallizzi r. Eur J Med Genet. 2015 Mar;58(3):188-90. doi: 10.1016/j.ejmg.2014.12.013. Epub 2015 Jan 13. Eur J Med Genet. 2015. PMID: 25595571
81 results