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Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy.
Santacroce R, Santoro R, Sessa F, Iannaccaro P, Sarno M, Longo V, Gallone A, Vecchione G, Muleo G, Margaglione M. Santacroce R, et al. Among authors: longo v. Blood Coagul Fibrinolysis. 2008 Apr;19(3):197-202. doi: 10.1097/MBC.0b013e3282f234ab. Blood Coagul Fibrinolysis. 2008. PMID: 18388498
Mutation analysis in hyperphenylalaninemia patients from South Italy.
Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Among authors: longo v. Clin Biochem. 2013 Dec;46(18):1896-8. doi: 10.1016/j.clinbiochem.2013.06.009. Epub 2013 Jun 18. Clin Biochem. 2013. PMID: 23792259
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.
Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Bafunno V, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Among authors: longo v. Clin Chim Acta. 2015 Oct 23;450:51-5. doi: 10.1016/j.cca.2015.07.014. Epub 2015 Jul 23. Clin Chim Acta. 2015. PMID: 26210745
A platelet defect modulates bleeding in mild hemophilia: the tale of 2 brothers.
Lapecorella M, Santacroce R, Napolitano M, Bafunno V, Favuzzi G, Longo V, Grandone E, Mariani G, Margaglione M. Lapecorella M, et al. Among authors: longo v. Clin Appl Thromb Hemost. 2009 Dec;15(6):715-6. doi: 10.1177/1076029609333676. Clin Appl Thromb Hemost. 2009. PMID: 19926614 Free article. No abstract available.
711 results