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Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: a genetic study of Sardinian family.
Concolino P, Satta MA, Santonocito C, Carrozza C, Rocchetti S, Ameglio F, Giardina E, Zuppi C, Capoluongo E. Concolino P, et al. Among authors: santonocito c. Clin Chim Acta. 2006 Feb;364(1-2):298-302. doi: 10.1016/j.cca.2005.07.020. Epub 2005 Sep 19. Clin Chim Acta. 2006. PMID: 16171792
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation.
Capoluongo E, Vento G, Santonocito C, Matassa PG, Vaccarella C, Giardina B, Romagnoli C, Zuppi C, Ameglio F. Capoluongo E, et al. Among authors: santonocito c. Eur Cytokine Netw. 2005 Sep;16(3):199-205. Eur Cytokine Netw. 2005. PMID: 16266860 Free article. Clinical Trial.
Slight association between type 1 diabetes and "ff" VDR FokI genotype in patients from the Italian Lazio Region. Lack of association with diabetes complications.
Capoluongo E, Pitocco D, Concolino P, Santonocito C, Di Stasio E, d'Onofrio G, Manto A, Giardina B, Ghirlanda G, Ameglio F, Zuppi C. Capoluongo E, et al. Among authors: santonocito c. Clin Biochem. 2006 Sep;39(9):888-92. doi: 10.1016/j.clinbiochem.2006.05.006. Epub 2006 May 26. Clin Biochem. 2006. PMID: 16806146
Epithelial lining fluid free IGF-I-to-PAPP-A ratio is associated with bronchopulmonary dysplasia in preterm infants.
Capoluongo E, Ameglio F, Lulli P, Minucci A, Santonocito C, Concolino P, Di Stasio E, Boccacci S, Vendettuoli V, Giuratrabocchetta G, De Cunto A, Tana M, Romagnoli C, Zuppi C, Vento G. Capoluongo E, et al. Among authors: santonocito c. Am J Physiol Endocrinol Metab. 2007 Jan;292(1):E308-13. doi: 10.1152/ajpendo.00251.2006. Epub 2006 Sep 5. Am J Physiol Endocrinol Metab. 2007. PMID: 16954333 Free article. Clinical Trial.
103 results