Santacroce R - Search Results

1

The Genetics of Hereditary Angioedema: A Review.

Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M. Santacroce R, et al. J Clin Med. 2021 May 9;10(9):2023. doi: 10.3390/jcm10092023. J Clin Med. 2021. PMID: 34065094 Free PMC article. Review.

2

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.

3

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

4

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

5

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.

6

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

7

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

8

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

9

Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors.

Coppola A, Margaglione M, Santagostino E, Rocino A, Grandone E, Mannucci PM, Di Minno G; AICE PROFIT Study Group. Coppola A, et al. J Thromb Haemost. 2009 Nov;7(11):1809-15. doi: 10.1111/j.1538-7836.2009.03615.x. Epub 2009 Sep 9. J Thromb Haemost. 2009. PMID: 19740093 Free article.

10

The risk of occurrence of venous thrombosis: focus on protein Z.

Bafunno V, Santacroce R, Margaglione M. Bafunno V, et al. Among authors: santacroce r. Thromb Res. 2011 Dec;128(6):508-15. doi: 10.1016/j.thromres.2011.08.007. Epub 2011 Aug 31. Thromb Res. 2011. PMID: 21885093 Review.

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