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Page 1
TLR2 and TLR4 gene polymorphisms and atopic dermatitis in Italian children: a multicenter study.
Salpietro C, Rigoli L, Miraglia Del Giudice M, Cuppari C, Di Bella C, Salpietro A, Maiello N, La Rosa M, Marseglia GL, Leonardi S, Briuglia S, Ciprandi G. Salpietro C, et al. Among authors: cuppari c. Int J Immunopathol Pharmacol. 2011 Oct;24(4 Suppl):33-40. doi: 10.1177/03946320110240S408. Int J Immunopathol Pharmacol. 2011. PMID: 22032785 Free article.
Serum IL-23 strongly and inversely correlates with FEV1 in asthmatic children.
Ciprandi G, Cuppari C, Salpietro AM, Tosca MA, Rigoli L, Grasso L, La Rosa M, Marseglia GL, Del Giudice MM, Salpietro C. Ciprandi G, et al. Among authors: cuppari c. Int Arch Allergy Immunol. 2012;159(2):183-6. doi: 10.1159/000336418. Epub 2012 Jun 1. Int Arch Allergy Immunol. 2012. PMID: 22678234
Serum IL-23 in asthmatic children.
Ciprandi G, Cuppari C, Salpietro A, Tosca M, Grasso L, Rigoli L, La Rosa M, Marseglia GL, Miraglia Del Giudice M, Salpietro C. Ciprandi G, et al. Among authors: cuppari c. J Biol Regul Homeost Agents. 2012 Jan-Mar;26(1 Suppl):S53-61. J Biol Regul Homeost Agents. 2012. PMID: 22691251
Nasal high-mobility group box-1 protein in children with allergic rhinitis.
Salpietro C, Cuppari C, Grasso L, Tosca MA, Miraglia Del Giudice M, La Rosa M, Marseglia GL, Salpietro A, Ciprandi G. Salpietro C, et al. Among authors: cuppari c. Int Arch Allergy Immunol. 2013;161(2):116-21. doi: 10.1159/000345246. Epub 2013 Jan 22. Int Arch Allergy Immunol. 2013. PMID: 23343652
Novel therapeutic targets for allergic airway disease in children.
Giallongo A, Parisi GF, Licari A, Pulvirenti G, Cuppari C, Salpietro C, Marseglia GL, Leonardi S. Giallongo A, et al. Among authors: cuppari c. Drugs Context. 2019 Jul 9;8:212590. doi: 10.7573/dic.212590. eCollection 2019. Drugs Context. 2019. PMID: 31391855 Free PMC article. Review.
HMGB1 modulation in children with allergic rhinitis.
Ciprandi G, Colavita L, Cuppari C, Tosca MA. Ciprandi G, et al. Among authors: cuppari c. Minerva Pediatr (Torino). 2023 Feb;75(1):127-128. doi: 10.23736/S2724-5276.20.05906-X. Epub 2020 Nov 17. Minerva Pediatr (Torino). 2023. PMID: 33203203 No abstract available.
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, Procaccio V, Striano P, Mankad K, Lieb A, Chen S, Pisani L, Bettencourt C, Männikkö R, Manole A, Brusco A, Grosso E, Ferrero GB, Armstrong-Moron J, Gueden S, Bar-Yosef O, Tzadok M, Monaghan KG, Santiago-Sim T, Person RE, Cho MT, Willaert R, Yoo Y, Chae JH, Quan Y, Wu H, Wang T, Bernier RA, Xia K, Blesson A, Jain M, Motazacker MM, Jaeger B, Schneider AL, Boysen K, Muir AM, Myers CT, Gavrilova RH, Gunderson L, Schultz-Rogers L, Klee EW, Dyment D, Osmond M, Parellada M, Llorente C, Gonzalez-Peñas J, Carracedo A, Van Haeringen A, Ruivenkamp C, Nava C, Heron D, Nardello R, Iacomino M, Minetti C, Skabar A, Fabretto A; SYNAPS Study Group; Raspall-Chaure M, Chez M, Tsai A, Fassi E, Shinawi M, Constantino JN, De Zorzi R, Fortuna S, Kok F, Keren B, Bonneau D, Choi M, Benzeev B, Zara F, Mefford HC, Scheffer IE, Clayton-Smith J, Macaya A, Rothman JE, Eichler EE, Kullmann DM, Houlden H. Salpietro V, et al. Nat Commun. 2019 Jul 12;10(1):3094. doi: 10.1038/s41467-019-10910-w. Nat Commun. 2019. PMID: 31300657 Free PMC article.
Hemodialysis in children: how, when and why.
Chimenz R, Fede C, Di Benedetto V, Concolino D, Scuderi MG, Salvo V, Gitto E, Cucinotta U, Viola V, Betta P, Cannavò L, Cuppari C. Chimenz R, et al. Among authors: cuppari c. J Biol Regul Homeost Agents. 2019 Sep-Oct;33(5 Suppl. 1):87-89. Special Issue: Focus on Pediatric Nephrology. J Biol Regul Homeost Agents. 2019. PMID: 31630720 Clinical Trial.
103 results