Menegatti M - Search Results

1

Molecular characterization of an Italian patient with plasminogen deficiency and ligneous conjunctivitis.

Siboni SM, Spreafico M, Menegatti M, Martinelli I, Peyvandi F. Siboni SM, et al. Among authors: menegatti m. Blood Coagul Fibrinolysis. 2007 Jan;18(1):81-4. doi: 10.1097/MBC.0b013e3280124f17. Blood Coagul Fibrinolysis. 2007. PMID: 17179833 Free article.

2

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. Thromb Res. 2001 Aug 15;103(4):299-307. doi: 10.1016/s0049-3848(01)00329-2. Thromb Res. 2001. PMID: 11562340

3

Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency.

Peyvandi F, Menegatti M, Santagostino E, Akhavan S, Uprichard J, Perry DJ, Perkins SJ, Mannucci PM. Peyvandi F, et al. Among authors: menegatti m. Br J Haematol. 2002 Jun;117(3):685-92. doi: 10.1046/j.1365-2141.2002.03486.x. Br J Haematol. 2002. PMID: 12028042 Free article.

4

Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations--a cause for concern.

Tripodi A, Peyvandi F, Chantarangkul V, Menegatti M, Mannucci PM. Tripodi A, et al. Among authors: menegatti m. Thromb Haemost. 2002 Oct;88(4):690-1. Thromb Haemost. 2002. PMID: 12362247 No abstract available.

5

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency.

Peyvandi F, Tagliabue L, Menegatti M, Karimi M, Komáromi I, Katona E, Muszbek L, Mannucci PM. Peyvandi F, et al. Among authors: menegatti m. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9206. Hum Mutat. 2004. PMID: 14695539

6

A rare inherited coagulation disorder: combined homozygous factor VII and factor X deficiency.

Menegatti M, Karimi M, Garagiola I, Mannucci P, Peyvandi F. Menegatti M, et al. Am J Hematol. 2004 Sep;77(1):90-1. doi: 10.1002/ajh.20132. Am J Hematol. 2004. PMID: 15307115 Free article.

7

Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations.

Tripodi A, Chantarangkul V, Menegatti M, Tagliabue L, Peyvandi F. Tripodi A, et al. Among authors: menegatti m. Clin Chem. 2005 Jul;51(7):1310-1. doi: 10.1373/clinchem.2005.049981. Clin Chem. 2005. PMID: 15976128 No abstract available.

8

Genetic diagnosis of haemophilia and other inherited bleeding disorders.

Peyvandi F, Jayandharan G, Chandy M, Srivastava A, Nakaya SM, Johnson MJ, Thompson AR, Goodeve A, Garagiola I, Lavoretano S, Menegatti M, Palla R, Spreafico M, Tagliabue L, Asselta R, Duga S, Mannucci PM. Peyvandi F, et al. Among authors: menegatti m. Haemophilia. 2006 Jul;12 Suppl 3:82-9. doi: 10.1111/j.1365-2516.2006.01263.x. Haemophilia. 2006. PMID: 16684001 Review.

9

Rare bleeding disorders.

Peyvandi F, Kaufman RJ, Seligsohn U, Salomon O, Bolton-Maggs PH, Spreafico M, Menegatti M, Palla R, Siboni S, Mannucci PM. Peyvandi F, et al. Among authors: menegatti m. Haemophilia. 2006 Jul;12 Suppl 3:137-42. doi: 10.1111/j.1365-2516.2006.01271.x. Haemophilia. 2006. PMID: 16684009 Free article. Review.

10

Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.

Karimi M, Menegatti M, Afrasiabi A, Sarikhani S, Peyvandi F. Karimi M, et al. Among authors: menegatti m. Haematologica. 2008 Jun;93(6):934-8. doi: 10.3324/haematol.12211. Epub 2008 Apr 9. Haematologica. 2008. PMID: 18403394 Free article.

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