Margaglione M - Search Results

1

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. Among authors: margaglione m. Haematologica. 2003 Dec;88(12):1378-82. Haematologica. 2003. PMID: 14687991

2

Detection of the factor V Leiden using SSCP.

Margaglione M, D'Andrea G, Cappucci G, Grandone E, Giuliani N, Colaizzo D, Vecchione G, Di Minno G. Margaglione M, et al. Thromb Haemost. 1996 Nov;76(5):814-5. Thromb Haemost. 1996. PMID: 8950796 No abstract available.

3

Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance.

Ames PR, Tommasino C, D'Andrea G, Iannaccone L, Brancaccio V, Margaglione M. Ames PR, et al. Among authors: margaglione m. Thromb Haemost. 1998 Jan;79(1):46-9. Thromb Haemost. 1998. PMID: 9459321

4

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

5

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

6

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. Among authors: margaglione m. Electrophoresis. 1998 Jun;19(8-9):1468-74. doi: 10.1002/elps.1150190842. Electrophoresis. 1998. PMID: 9694297

7

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. Among authors: margaglione m. 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

8

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

9

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

10

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

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