Castaman G - Search Results

1

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.

Castaman G, Lethagen S, Federici AB, Tosetto A, Goodeve A, Budde U, Batlle J, Meyer D, Mazurier C, Fressinaud E, Goudemand J, Eikenboom J, Schneppenheim R, Ingerslev J, Vorlova Z, Habart D, Holmberg L, Pasi J, Hill F, Peake I, Rodeghiero F. Castaman G, et al. Blood. 2008 Apr 1;111(7):3531-9. doi: 10.1182/blood-2007-08-109231. Epub 2008 Jan 29. Blood. 2008. PMID: 18230755 Free article. Clinical Trial.

2

The factor VIII/von Willebrand factor ratio discriminates between reduced synthesis and increased clearance of von Willebrand factor.

Eikenboom JC, Castaman G, Kamphuisen PW, Rosendaal FR, Bertina RM. Eikenboom JC, et al. Among authors: castaman g. Thromb Haemost. 2002 Feb;87(2):252-7. Thromb Haemost. 2002. PMID: 11859851

3

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

4

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.

5

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.

6

ABO blood group also influences the von Willebrand factor (VWF) antigen level in heterozygous carriers of VWF null alleles, type 2N mutation Arg854GIn, and the missense mutation Cys2362Phe.

Castaman G, Eikenboom JC. Castaman G, et al. Blood. 2002 Sep 1;100(5):1927-8. doi: 10.1182/blood-2002-04-1168. Blood. 2002. PMID: 12211196 Free article. No abstract available.

7

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.

8

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.

9

Fluorescent polymerase chain reaction and capillary electrophoresis for IgH rearrangement and minimal residual disease evaluation in multiple myeloma.

Novella E, Giaretta I, Elice F, Madeo D, Piccin A, Castaman G, Rodeghiero F. Novella E, et al. Among authors: castaman g. Haematologica. 2002 Nov;87(11):1157-64. Haematologica. 2002. PMID: 12414345

10

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.

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