Mingozzi F - Search Results

1

Illustrated State-of-the-Art Capsules of the ISTH 2020 Congress.

Ariens R, Becattini C, Bender M, Bergmeier W, Castoldi E, Devreese K, Ellis M, Gailani D, Ignjatovic V, James PD, Kerrigan S, Lambert M, Lee LH, Levi M, Maugeri N, Meijers J, Melero-Martin J, Michelson AD, Mingozzi F, Neeves K, Ni H, Olsson AK, Prohászka Z, Ranson M, Riva N, Senis Y, van Ommen CH, Vaughan DE, Weisel J. Ariens R, et al. Among authors: mingozzi f. Res Pract Thromb Haemost. 2020 Jul 12;4(5):680-713. doi: 10.1002/rth2.12368. eCollection 2020 Jul. Res Pract Thromb Haemost. 2020. PMID: 32685876 Free PMC article.

2

A FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers.

Mingozzi F, Legnani C, Lunghi B, Scanavini D, Castoldi E, Palareti G, Marchetti G, Bernardi F. Mingozzi F, et al. Thromb Haemost. 2003 Jun;89(6):983-9. Thromb Haemost. 2003. PMID: 12783110

3

New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians.

Castoldi E, Lunghi B, Mingozzi F, Ioannou P, Marchetti G, Bernardi F. Castoldi E, et al. Among authors: mingozzi f. Thromb Haemost. 1997 Sep;78(3):1037-41. Thromb Haemost. 1997. PMID: 9308750

4

Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma.

Castoldi E, Rosing J, Girelli D, Hoekema L, Lunghi B, Mingozzi F, Ferraresi P, Friso S, Corrocher R, Tans G, Bernardi F. Castoldi E, et al. Among authors: mingozzi f. Thromb Haemost. 2000 Mar;83(3):362-5. Thromb Haemost. 2000. PMID: 10744138

5

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: mingozzi f. Haematologica. 2001 Jun;86(6):629-33. Haematologica. 2001. PMID: 11418372

6

The factor VIII D1241E polymorphism is associated with decreased factor VIII activity and not with activated protein C resistance levels.

Scanavini D, Legnani C, Lunghi B, Mingozzi F, Palareti G, Bernardi F. Scanavini D, et al. Among authors: mingozzi f. Thromb Haemost. 2005 Mar;93(3):453-6. doi: 10.1160/TH04-09-0629. Thromb Haemost. 2005. PMID: 15735794

7

A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders.

Castoldi E, Lunghi B, Mingozzi F, Simioni P, Girolami A, Bernardi F. Castoldi E, et al. Among authors: mingozzi f. Br J Haematol. 2001 Sep;114(4):868-70. doi: 10.1046/j.1365-2141.2001.03052.x. Br J Haematol. 2001. PMID: 11564076 Free article.

8

A new factor V gene polymorphism (His 1254 Arg) present in subjects of african origin mimics the R2 polymorphism (His 1299 Arg).

Lunghi B, Castoldi E, Mingozzi F, Bernardi F. Lunghi B, et al. Among authors: mingozzi f. Blood. 1998 Jan 1;91(1):364-5. Blood. 1998. PMID: 9414311 Free article. No abstract available.

9

Recombinant Adeno-Associated Viral Vectors Expressing Human Coagulation FIX-E456H Variant in Hemophilia B Mice.

Le Quellec S, Dane AP, Barbon E, Bordet JC, Mingozzi F, Dargaud Y, Marais T, Biferi MG, Négrier C, Nathawani AC, Enjolras N. Le Quellec S, et al. Among authors: mingozzi f. Thromb Haemost. 2019 Dec;119(12):1956-1967. doi: 10.1055/s-0039-1697658. Epub 2019 Oct 28. Thromb Haemost. 2019. PMID: 31659733

10

A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject.

Lunghi B, Castoldi E, Mingozzi F, Bernardi F, Castaman G. Lunghi B, et al. Among authors: mingozzi f. Blood. 1998 Aug 15;92(4):1463-4. Blood. 1998. PMID: 9694743 Free article. No abstract available.

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