Castaman G - Search Results

1

Obstetric complications and pregnancy-related venous thromboembolism: the effect of low-molecular-weight heparin on their prevention in carriers of factor V Leiden or prothrombin G20210A mutation.

Tormene D, Grandone E, De Stefano V, Tosetto A, Palareti G, Margaglione M, Castaman G, Rossi E, Ciminello A, Valdrè L, Legnani C, Tiscia GL, Bafunno V, Carraro S, Rodeghiero F, Simioni P. Tormene D, et al. Among authors: castaman g. Thromb Haemost. 2012 Mar;107(3):477-84. doi: 10.1160/TH11-07-0470. Epub 2012 Jan 25. Thromb Haemost. 2012. PMID: 22273731

2

A novel family with recessive von Willebrand disease due to compound heterozygosity for a splice site mutation and a missense mutation in the von Willebrand factor gene.

Castaman G, Novella E, Castiglia E, Eikenboom JC, Rodeghiero F. Castaman G, et al. Thromb Res. 2002 Jan 15;105(2):135-8. doi: 10.1016/s0049-3848(02)00007-5. Thromb Res. 2002. PMID: 11958803

3

The elusive pathogenesis of von Willebrand disease Vicenza.

Castaman G, Rodeghiero F, Mannucci PM. Castaman G, et al. Blood. 2002 Jun 1;99(11):4243-4; author reply 4244. doi: 10.1182/blood.v99.11.4243. Blood. 2002. PMID: 12043692 Free article. No abstract available.

4

Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia.

Faioni EM, Franchi F, Castaman G, Biguzzi E, Rodeghiero F. Faioni EM, et al. Among authors: castaman g. Br J Haematol. 2002 Aug;118(2):595-9. doi: 10.1046/j.1365-2141.2002.03644.x. Br J Haematol. 2002. PMID: 12139752 Free article.

5

Factor V Leiden mutation carriership and venous thromboembolism in polycythemia vera and essential thrombocythemia.

Ruggeri M, Gisslinger H, Tosetto A, Rintelen C, Mannhalter C, Pabinger I, Heis N, Castaman G, Missiaglia E, Lechner K, Rodeghiero F. Ruggeri M, et al. Among authors: castaman g. Am J Hematol. 2002 Sep;71(1):1-6. doi: 10.1002/ajh.10153. Am J Hematol. 2002. PMID: 12221665 Free article.

6

First Italian families with homozygous R854Q type 2 N von Willebrand disease.

Castaman G, Novella E, Contino L, Demicheli M, Rodeghiero F. Castaman G, et al. Thromb Haemost. 2002 Sep;88(3):534-5. Thromb Haemost. 2002. PMID: 12353087 No abstract available.

7

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment.

Castaman G, Federici AB, Rodeghiero F, Mannucci PM. Castaman G, et al. Haematologica. 2003 Jan;88(1):94-108. Haematologica. 2003. PMID: 12551832 Free article. Review.

8

The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis.

Castaman G, Faioni EM, Tosetto A, Bernardi F. Castaman G, et al. Haematologica. 2003 Oct;88(10):1182-9. Haematologica. 2003. PMID: 14555316

9

Association of factor V deficiency with factor V HR2.

Faioni EM, Castaman G, Asti D, Lussana F, Rodeghiero F. Faioni EM, et al. Among authors: castaman g. Haematologica. 2004 Feb;89(2):195-200. Haematologica. 2004. PMID: 15003895

10

Treatment of von Willebrand disease.

Rodeghiero F, Castaman G. Rodeghiero F, et al. Among authors: castaman g. Semin Hematol. 2005 Jan;42(1):29-35. doi: 10.1053/j.seminhematol.2004.10.001. Semin Hematol. 2005. PMID: 15662613 Review.

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