Asselta R - Search Results

1

Impact of chronic exposure to 5-alpha reductase inhibitors on the risk of hospitalization for COVID-19: a case-control study in male population from two COVID-19 regional centers of Lombardy, Italy.

Lazzeri M, Duga S, Azzolini E, Fasulo V, Buffi N, Saita A, Lughezzani G, Paraboschi EM, Hurle R, Nobili A, Cecconi M, Guazzoni G, Casale P, Asselta R; Humanitas COVID-19 Task Force, The Humanitas Gavazzeni COVID-19 Task Force. Lazzeri M, et al. Among authors: asselta r. Minerva Urol Nephrol. 2022 Feb;74(1):77-84. doi: 10.23736/S2724-6051.20.04081-3. Epub 2021 Jan 13. Minerva Urol Nephrol. 2022. PMID: 33439572 Free article.

2

Identification of a glucocorticoid response element in the human gamma chain fibrinogen promoter.

Asselta R, Duga S, Modugno M, Malcovati M, Tenchini ML. Asselta R, et al. Thromb Haemost. 1998 Jun;79(6):1144-50. Thromb Haemost. 1998. PMID: 9657439 Free article.

3

Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.

Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Haematologica. 2002 Aug;87(8):855-9. Haematologica. 2002. PMID: 12161363

4

Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein.

Duga S, Montefusco MC, Asselta R, Malcovati M, Peyvandi F, Santagostino E, Mannucci PM, Tenchini ML. Duga S, et al. Among authors: asselta r. Blood. 2003 Jan 1;101(1):173-7. doi: 10.1182/blood-2002-06-1928. Epub 2002 Aug 15. Blood. 2003. PMID: 12393490 Free article.

5

Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites.

Spena S, Duga S, Asselta R, Malcovati M, Peyvandi F, Tenchini ML. Spena S, et al. Among authors: asselta r. Blood. 2002 Dec 15;100(13):4478-84. doi: 10.1182/blood-2002-06-1647. Epub 2002 Aug 1. Blood. 2002. PMID: 12393540 Free article.

6

Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations.

Montefusco MC, Duga S, Asselta R, Malcovati M, Peyvandi F, Santagostino E, Mannucci PM, Tenchini ML. Montefusco MC, et al. Among authors: asselta r. Blood. 2003 Nov 1;102(9):3210-6. doi: 10.1182/blood-2003-03-0922. Epub 2003 Jun 19. Blood. 2003. PMID: 12816860 Free article.

7

Missense or splicing mutation? The case of a fibrinogen Bbeta-chain mutation causing severe hypofibrinogenemia.

Asselta R, Duga S, Spena S, Peyvandi F, Castaman G, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Blood. 2004 Apr 15;103(8):3051-4. doi: 10.1182/blood-2003-10-3725. Epub 2003 Dec 24. Blood. 2004. PMID: 15070683 Free article.

8

Coagulation factor V.

Duga S, Asselta R, Tenchini ML. Duga S, et al. Among authors: asselta r. Int J Biochem Cell Biol. 2004 Aug;36(8):1393-9. doi: 10.1016/j.biocel.2003.08.002. Int J Biochem Cell Biol. 2004. PMID: 15147718 Review.

9

Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.

Spena S, Duga S, Asselta R, Peyvandi F, Mahasandana C, Malcovati M, Tenchini ML. Spena S, et al. Among authors: asselta r. Eur J Hum Genet. 2004 Nov;12(11):891-8. doi: 10.1038/sj.ejhg.5201207. Eur J Hum Genet. 2004. PMID: 15489905

10

Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.

Zadra G, Asselta R, Malcovati M, Santagostino E, Peyvandi F, Mannucci PM, Tenchini ML, Duga S. Zadra G, et al. Among authors: asselta r. Haematologica. 2004 Nov;89(11):1332-40. Haematologica. 2004. PMID: 15531455 Free article.

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