Malcovati M - Search Results

1

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. Among authors: malcovati m. Thromb Haemost. 1998 Jun;79(6):1144-50. Thromb Haemost. 1998. PMID: 9657439 Free article.

2

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. Among authors: malcovati m. Haematologica. 2002 Aug;87(8):855-9. Haematologica. 2002. PMID: 12161363

3

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: malcovati m. 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.

4

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. Among authors: malcovati m. 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.

5

Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.

Monaldini L, Asselta R, Duga S, Peyvandi F, Karimi M, Malcovati M, Tenchini ML. Monaldini L, et al. Among authors: malcovati m. Thromb Haemost. 2007 Apr;97(4):546-51. Thromb Haemost. 2007. PMID: 17393016

6

Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML. Duga S, et al. Among authors: malcovati m. Blood. 2000 Feb 15;95(4):1336-41. Blood. 2000. PMID: 10666208 Free article.

7

Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.

Asselta R, Duga S, Simonic T, Malcovati M, Santagostino E, Giangrande PL, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: malcovati m. Blood. 2000 Oct 1;96(7):2496-500. Blood. 2000. PMID: 11001902 Free article.

8

Identification of four novel polymorphisms in the Aalpha and gamma fibrinogen genes and analysis of association with plasma levels of the protein.

Menegatti M, Asselta R, Duga S, Malcovati M, Bucciarelli P, Mannucci PM, Tenchini ML. Menegatti M, et al. Among authors: malcovati m. Thromb Res. 2001 Aug 15;103(4):299-307. doi: 10.1016/s0049-3848(01)00329-2. Thromb Res. 2001. PMID: 11562340

9

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.

Asselta R, Duga S, Spena S, Santagostino E, Peyvandi F, Piseddu G, Targhetta R, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: malcovati m. Blood. 2001 Dec 15;98(13):3685-92. doi: 10.1182/blood.v98.13.3685. Blood. 2001. PMID: 11739173 Free article.

10

Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.

Asselta R, Montefusco MC, Duga S, Malcovati M, Peyvandi F, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: malcovati m. J Thromb Haemost. 2003 Jun;1(6):1237-44. doi: 10.1046/j.1538-7836.2003.00160.x. J Thromb Haemost. 2003. PMID: 12871325 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

72 results

Search Page

Filters