Santacroce R - Search Results

1

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: santacroce r. 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

2

Factor V Arg2074Cys: a novel missense mutation in the C2 domain of factor V.

Bossone A, D'Angelo F, Santacroce R, De Lucia D, Margaglione M. Bossone A, et al. Among authors: santacroce r. Thromb Haemost. 2002 May;87(5):923-4. Thromb Haemost. 2002. PMID: 12038802 No abstract available.

3

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

D'Andrea G, D'Ambrosio RL, Di Perna P, Chetta M, Santacroce R, Brancaccio V, Grandone E, Margaglione M. D'Andrea G, et al. Among authors: santacroce r. Blood. 2005 Jan 15;105(2):645-9. doi: 10.1182/blood-2004-06-2111. Epub 2004 Sep 9. Blood. 2005. PMID: 15358623 Free article. Clinical Trial.

4

Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.

Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M. Santacroce R, et al. Blood Coagul Fibrinolysis. 2006 Jun;17(4):235-40. doi: 10.1097/01.mbc.0000224841.48463.be. Blood Coagul Fibrinolysis. 2006. PMID: 16651864

5

A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients.

D'Ambrosio R, Santacroce R, Di Perna P, Sarno M, Romondia A, Margaglione M. D'Ambrosio R, et al. Among authors: santacroce r. Blood Coagul Fibrinolysis. 2007 Mar;18(2):203-4. doi: 10.1097/MBC.0b013e328012b615. Blood Coagul Fibrinolysis. 2007. PMID: 17287640

6

The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype.

Margaglione M, Castaman G, Morfini M, Rocino A, Santagostino E, Tagariello G, Tagliaferri AR, Zanon E, Bicocchi MP, Castaldo G, Peyvandi F, Santacroce R, Torricelli F, Grandone E, Mannucci PM; AICE-Genetics Study Group. Margaglione M, et al. Among authors: santacroce r. Haematologica. 2008 May;93(5):722-8. doi: 10.3324/haematol.12427. Epub 2008 Apr 2. Haematologica. 2008. PMID: 18387975 Free article.

7

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. Blood Coagul Fibrinolysis. 2008 Apr;19(3):197-202. doi: 10.1097/MBC.0b013e3282f234ab. Blood Coagul Fibrinolysis. 2008. PMID: 18388498

8

Coexistence of beta-thalassemia and hereditary hemochromatosis in homozygosity: a possible synergic effect?

Bukvic N, Sportelli F, Sessa F, Longo V, Roberti MG, Santacroce R, Margaglione M. Bukvic N, et al. Among authors: santacroce r. Hemoglobin. 2009;33(2):155-7. doi: 10.1080/03630260902817354. Hemoglobin. 2009. PMID: 19373593

9

Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification.

Santacroce R, Longo V, Bafunno V, Sessa F, Chetta M, Sarno M, Bukvic N, D'Andrea G, Tomaiuolo M, Margaglione M. Santacroce R, et al. Genet Test Mol Biomarkers. 2009 Oct;13(5):573-6. doi: 10.1089/gtmb.2009.0015. Genet Test Mol Biomarkers. 2009. PMID: 19715469

10

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: santacroce r. 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.

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