Di Minno G - Search Results

1

A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.

Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G. Margaglione M, et al. Among authors: di minno g. Thromb Haemost. 2001 Dec;86(6):1483-8. Thromb Haemost. 2001. PMID: 11776317

2

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. Among authors: di minno g. Thromb Haemost. 2002 Jun;87(6):1034-42. Thromb Haemost. 2002. PMID: 12083483

3

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: di minno g. Thromb Haemost. 1997 May;77(5):822-4. Thromb Haemost. 1997. PMID: 9184385

4

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: di minno g. Thromb Haemost. 1998 Nov;80(5):805-10. Thromb Haemost. 1998. PMID: 9843175

5

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. Among authors: di minno g. Thromb Haemost. 1999 Apr;81(4):486-92. Thromb Haemost. 1999. PMID: 10235425

6

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: di minno g. Thromb Haemost. 1999 Jul;82(1):19-23. Thromb Haemost. 1999. PMID: 10456448

7

A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.

Margaglione M, Santacroce R, Colaizzo D, Seripa D, Vecchione G, Lupone MR, De Lucia D, Fortina P, Grandone E, Perricone C, Di Minno G. Margaglione M, et al. Among authors: di minno g. Blood. 2000 Oct 1;96(7):2501-5. Blood. 2000. PMID: 11001903 Free article.

8

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. Among authors: di perna p, di minno g. Haematologica. 2003 Apr;88(4):459-64. Haematologica. 2003. PMID: 12681974

9

Raised plasma fibrinogen concentrations in subjects attending a metabolic ward--relation to family history and vascular risk factors.

Margaglione M, Di Minno G, Grandone E, Vecchione G, Celentano E, Cappucci G, Giordano M, Grilli M, Simone P, Fusilli S, et al. Margaglione M, et al. Among authors: di minno g. Thromb Haemost. 1995 Apr;73(4):579-83. Thromb Haemost. 1995. PMID: 7495062

10

Clinical relevance of polymorphic markers of arterial thrombosis.

Di Minno G, Grandone E, Margaglione M. Di Minno G, et al. Thromb Haemost. 1997 Jul;78(1):462-6. Thromb Haemost. 1997. PMID: 9198197 Review.

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