D'Andrea G - Search Results

1

Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia.

D'Andrea G, Schiavulli M, Dimatteo C, Santacroce R, Guerra E, Longo VA, Grandone E, Margaglione M. D'Andrea G, et al. Blood. 2013 Dec 19;122(26):4289-91. doi: 10.1182/blood-2013-09-528943. Blood. 2013. PMID: 24357714 Free article. No abstract available.

2

The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.

Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G. Margaglione M, et al. Thromb Haemost. 1998 May;79(5):907-11. Thromb Haemost. 1998. PMID: 9609218

3

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

4

Identifying human platelet glycoproteins IIb and IIIa by capillary electrophoresis.

Vecchione G, Margaglione M, Grandone E, Colaizzo D, Cappucci G, Giuliani N, d'Addedda M, D'Andrea G, Nobile M, Amoriello A, Di Minno G. Vecchione G, et al. Electrophoresis. 1998 Jun;19(8-9):1468-74. doi: 10.1002/elps.1150190842. Electrophoresis. 1998. PMID: 9694297

5

Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.

Grandone E, Margaglione M, Colaizzo D, D'Andrea G, Cappucci G, Brancaccio V, Di Minno G. Grandone E, et al. Am J Obstet Gynecol. 1998 Nov;179(5):1324-8. doi: 10.1016/s0002-9378(98)70155-3. Am J Obstet Gynecol. 1998. PMID: 9822524

6

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

7

Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden.

Margaglione M, D'Andrea G, Giuliani N, Brancaccio V, De Lucia D, Grandone E, De Stefano V, Tonali PA, Di Minno G. Margaglione M, et al. Arterioscler Thromb Vasc Biol. 1999 Jul;19(7):1751-6. doi: 10.1161/01.atv.19.7.1751. Arterioscler Thromb Vasc Biol. 1999. PMID: 10397694

8

Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism.

Margaglione M, D'Andrea G, Colaizzo D, Cappucci G, del Popolo A, Brancaccio V, Ciampa A, Grandone E, Di Minno G. Margaglione M, et al. Thromb Haemost. 1999 Dec;82(6):1583-7. Thromb Haemost. 1999. PMID: 10613638

9

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.

10

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

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