D'Andrea G - 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

Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.

Margaglione M, Brancaccio V, Giuliani N, D'Andrea G, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Di Minno G. Margaglione M, et al. Ann Intern Med. 1998 Jul 15;129(2):89-93. doi: 10.7326/0003-4819-129-2-199807150-00003. Ann Intern Med. 1998. PMID: 9669991

3

High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis.

Amitrano L, Brancaccio V, Guardascione MA, Margaglione M, Iannaccone L, Dandrea G, Ames PR, Marmo R, Mosca S, Balzano A. Amitrano L, et al. Am J Gastroenterol. 2001 Jan;96(1):146-9. doi: 10.1111/j.1572-0241.2001.03465.x. Am J Gastroenterol. 2001. PMID: 11197244

4

Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients.

D'Andrea G, Colaizzo D, Vecchione G, Grandone E, Di Minno G, Margaglione M; GLAnzmann's Thrombasthenia Italian Team (GLATIT). D'Andrea G, et al. Thromb Haemost. 2002 Jun;87(6):1034-42. Thromb Haemost. 2002. PMID: 12083483

5

The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation.

Bossone A, Cappucci F, D'Andrea G, Brancaccio V, Cibelli G, Iannaccone L, Grandone E, Margaglione M. Bossone A, et al. Haematologica. 2003 Mar;88(3):286-9. Haematologica. 2003. PMID: 12651267

6

A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency.

D'Andrea G, Di Perna P, Brancaccio V, Faioni EM, Castaman G, Cibelli G, Di Minno G, Margaglione M; Protein S Italian Team. D'Andrea G, et al. Haematologica. 2003 Apr;88(4):459-64. Haematologica. 2003. PMID: 12681974

7

Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism.

D'Andrea G, Margaglione M; Glansmann's Thrombasthemia Italian Team (GLATIT). D'Andrea G, et al. Haematologica. 2003 Dec;88(12):1378-82. Haematologica. 2003. PMID: 14687991

8

Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain.

D'Andrea G, Bossone A, Lupone MR, Peyvandi F, Maisto G, Perricone F, Grandone E, Margaglione M. D'Andrea G, et al. Haematologica. 2004 Aug;89(8):979-84. Haematologica. 2004. PMID: 15339682

9

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. 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.

10

Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin.

D'Ambrosio RL, D'Andrea G, Cappucci F, Chetta M, Di Perna P, Brancaccio V, Grandone E, Margaglione M. D'Ambrosio RL, et al. Haematologica. 2004 Dec;89(12):1510-6. Haematologica. 2004. PMID: 15590403

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