D'Andrea G - Search Results

1

Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin.

Andriulli A, Di Marco V, Margaglione M, Ippolito AM, Fattovich G, Smedile A, Valvano MR, Calvaruso V, Gioffreda D, Milella M, Morisco F, Felder M, Brancaccio G, Fasano M, Gatti P, Tundo P, Barone M, Cozzolongo R, Angelico M, D'Andrea G, Andriulli N, Abate ML, Mazzella G, Gaeta GB, Craxi A, Santantonio T. Andriulli A, et al. J Hepatol. 2014 Jan;60(1):16-21. doi: 10.1016/j.jhep.2013.07.040. Epub 2013 Aug 20. J Hepatol. 2014. PMID: 23973930 Free article.

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

Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib alpha gene in a patient with a severe bleeding tendency.

Margaglione M, D'Andrea G, Grandone E, Brancaccio V, Amoriello A, Di Minno G. Margaglione M, et al. Thromb Haemost. 1999 Apr;81(4):486-92. Thromb Haemost. 1999. PMID: 10235425

4

Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis.

Amitrano L, Brancaccio V, Guardascione MA, Margaglione M, Iannaccone L, D'Andrea G, Marmo R, Ames PR, Balzano A. Amitrano L, et al. Hepatology. 2000 Feb;31(2):345-8. doi: 10.1002/hep.510310213. Hepatology. 2000. PMID: 10655256

5

Genetic modulation of oral anticoagulation with warfarin.

Margaglione M, Colaizzo D, D'Andrea G, Brancaccio V, Ciampa A, Grandone E, Di Minno G. Margaglione M, et al. Thromb Haemost. 2000 Nov;84(5):775-8. Thromb Haemost. 2000. PMID: 11127854 Clinical Trial.

6

FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile.

Margaglione M, Bossone A, Coalizzo D, D'Andrea G, Brancaccio V, Ciampa A, Grandone E, Di MG. Margaglione M, et al. Thromb Haemost. 2002 Jan;87(1):32-6. Thromb Haemost. 2002. PMID: 11848454

7

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

8

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

9

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

10

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

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