Cappucci G - Search Results

1

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. Among authors: cappucci g. Thromb Haemost. 1998 May;79(5):907-11. Thromb Haemost. 1998. PMID: 9609218

2

Factor V Leiden is associated with repeated and recurrent unexplained fetal losses.

Grandone E, Margaglione M, Colaizzo D, d'Addedda M, Cappucci G, Vecchione G, Sciannamé N, Pavone G, Di Minno G. Grandone E, et al. Among authors: cappucci g. Thromb Haemost. 1997 May;77(5):822-4. Thromb Haemost. 1997. PMID: 9184385

3

Factor V Leiden, C > T MTHFR polymorphism and genetic susceptibility to preeclampsia.

Grandone E, Margaglione M, Colaizzo D, Cappucci G, Paladini D, Martinelli P, Montanaro S, Pavone G, Di Minno G. Grandone E, et al. Among authors: cappucci g. Thromb Haemost. 1997 Jun;77(6):1052-4. Thromb Haemost. 1997. PMID: 9241730

4

The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease.

Margaglione M, Cappucci G, Colaizzo D, Giuliani N, Vecchione G, Grandone E, Pennelli O, Di Minno G. Margaglione M, et al. Among authors: cappucci g. Arterioscler Thromb Vasc Biol. 1998 Feb;18(2):152-6. doi: 10.1161/01.atv.18.2.152. Arterioscler Thromb Vasc Biol. 1998. PMID: 9484978

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. Among authors: cappucci g. 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

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: cappucci g. 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

7

Fibrinogen plasma levels in an apparently healthy general population--relation to environmental and genetic determinants.

Margaglione M, Cappucci G, Colaizzo D, Pirro L, Vecchione G, Grandone E, Di Minno G. Margaglione M, et al. Among authors: cappucci g. Thromb Haemost. 1998 Nov;80(5):805-10. Thromb Haemost. 1998. PMID: 9843175

8

Prothrombotic genetic risk factors and the occurrence of gestational hypertension with or without proteinuria.

Grandone E, Margaglione M, Colaizzo D, Cappucci G, Sciannamé N, Montanaro S, Paladini D, Martinelli P, Di Minno G. Grandone E, et al. Among authors: cappucci g. Thromb Haemost. 1999 Mar;81(3):349-52. Thromb Haemost. 1999. PMID: 10102458

9

Genetic polymorphism of 5,10-MTHFR reductase gene in offspring of patients with myocardial infarction.

Margaglione M, Colaizzo D, Cappucci G, del Popolo A, Vecchione G, Grandone E, Di Minno G. Margaglione M, et al. Among authors: cappucci g. Thromb Haemost. 1999 Jul;82(1):19-23. Thromb Haemost. 1999. PMID: 10456448

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. Among authors: cappucci g. Thromb Haemost. 1999 Dec;82(6):1583-7. Thromb Haemost. 1999. PMID: 10613638

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