Redaelli R - Search Results

1

The factor V Glu1608Lys mutation is recurrent in familial thrombophilia.

Lunghi B, Scanavini D, Castoldi E, Gemmati D, Tognazzo S, Redaelli R, Ghirarduzzi A, Ieran M, Pinotti M, Bernardi F. Lunghi B, et al. Among authors: redaelli r. J Thromb Haemost. 2005 Sep;3(9):2032-8. doi: 10.1111/j.1538-7836.2005.01453.x. Epub 2005 Jun 24. J Thromb Haemost. 2005. PMID: 15975136 Free article.

2

Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma.

Lunghi B, Iacoviello L, Gemmati D, Dilasio MG, Castoldi E, Pinotti M, Castaman G, Redaelli R, Mariani G, Marchetti G, Bernardi F. Lunghi B, et al. Among authors: redaelli r. Thromb Haemost. 1996 Jan;75(1):45-8. Thromb Haemost. 1996. PMID: 8713778

3

A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population.

Castoldi E, Lunghi B, Mingozzi F, Muleo G, Redaelli R, Mariani G, Bernardi F. Castoldi E, et al. Among authors: redaelli r. Haematologica. 2001 Jun;86(6):629-33. Haematologica. 2001. PMID: 11418372

4

Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region.

Bernardi F, Patracchini P, Gemmati D, Ferrati M, Arcieri P, Papacchini M, Redaelli R, Baudo F, Mariani G, Marchetti G. Bernardi F, et al. Among authors: redaelli r. Hum Genet. 1993 Nov;92(5):446-50. doi: 10.1007/BF00216448. Hum Genet. 1993. PMID: 8244334

5

Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.

Pinotti M, Toso R, Redaelli R, Berrettini M, Marchetti G, Bernardi F. Pinotti M, et al. Among authors: redaelli r. Blood. 1998 Sep 1;92(5):1646-51. Blood. 1998. PMID: 9716592 Free article.

6

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.

Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, Pinotti M, Redaelli R, Ballerini G, Pemberton S, et al. Bernardi F, et al. Among authors: redaelli r. Br J Haematol. 1994 Mar;86(3):610-8. doi: 10.1111/j.1365-2141.1994.tb04793.x. Br J Haematol. 1994. PMID: 8043443

7

A missense mutation (178Cys-->Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene.

Marchetti G, Ferrati M, Patracchini P, Redaelli R, Bernardi F. Marchetti G, et al. Among authors: redaelli r. Hum Mol Genet. 1993 Jul;2(7):1055-6. doi: 10.1093/hmg/2.7.1055. Hum Mol Genet. 1993. PMID: 8364544 No abstract available.

8

Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro).

Bernardi F, Castaman G, Redaelli R, Pinotti M, Lunghi B, Rodeghiero F, Marchetti G. Bernardi F, et al. Among authors: redaelli r. Hum Mol Genet. 1994 Jul;3(7):1175-7. doi: 10.1093/hmg/3.7.1175. Hum Mol Genet. 1994. PMID: 7981691 No abstract available.

9

Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors.

Lunghi B, Redaelli R, Caimi TM, Corno AR, Bernardi F, Marchetti G. Lunghi B, et al. Among authors: redaelli r. Haemophilia. 2011 Sep;17(5):822-4. doi: 10.1111/j.1365-2516.2011.02524.x. Epub 2011 Mar 24. Haemophilia. 2011. PMID: 21435120 No abstract available.

10

von Willebrand factor ristocetin cofactor (VWF:RCo) assay: implementation on an automated coagulometer (ACL).

Redaelli R, Corno AR, Borroni L, Mostarda G, Nichelatti M, Morra E, Baudo F. Redaelli R, et al. J Thromb Haemost. 2005 Dec;3(12):2684-8. doi: 10.1111/j.1538-7836.2005.01628.x. J Thromb Haemost. 2005. PMID: 16359507 Free article.

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