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Research Output

2019

Analysis of factor V in zebrafish demonstrates minimal levels needed for early hemostasis

Weyand, A. C., Grzegorski, S. J., Rost, M. S., Lavik, K. I., Ferguson, A. C., Menegatti, M., Richter, C. E., Asselta, R., Duga, S., Peyvandi, F. & Shavit, J. A., Jun 11 2019, In : Blood advances. 3, 11, p. 1670-1680 11 p.

Research output: Contribution to journalArticle

Open Access

Clinical and laboratory diagnosis of rare coagulation disorders (RCDs)

Menegatti, M. & Palla, R., Jan 1 2019, (Accepted/In press) In : Thrombosis Research.

Research output: Contribution to journalArticle

Management of rare acquired bleeding disorders

Menegatti, M., Biguzzi, E. & Peyvandi, F., Dec 6 2019, In : Hematology (United States). 2019, 1, p. 80-87 8 p.

Research output: Contribution to journalArticle

Open Access

Treatment of rare factor deficiencies other than hemophilia

Menegatti, M. & Peyvandi, F., Jan 31 2019, In : Blood. 133, 5, p. 415-424 10 p.

Research output: Contribution to journalReview article

Open Access
2018

Molecular investigation of 41 patients affected by coagulation factor XI deficiency

Rimoldi, V., Paraboschi, E. M., Menegatti, M., Peyvandi, F., Salomon, O., Duga, S. & Asselta, R., 2018, In : Haemophilia. 24, 2, p. e50-e55

Research output: Contribution to journalArticle

Recombinant factor XIII A-subunit in a patient with factor XIII deficiency and recurrent pregnancy loss

Al-Khabori, M., Pathare, A., Menegatti, M. & Peyvandi, F., Jun 1 2018, In : Journal of Thrombosis and Haemostasis. 16, 6, p. 1052-1054 3 p.

Research output: Contribution to journalComment/debate

2017

Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO-RBDD project laboratories

Jennings, I., Kitchen, S., Menegatti, M., Palla, R., Walker, I., Makris, M. & Peyvandi, F., Aug 1 2017, In : International Journal of Laboratory Hematology. 39, 4, p. 350-358 9 p.

Research output: Contribution to journalArticle

Exploring the global landscape of genetic variation in coagulation factor XI deficiency

Asselta, R., Paraboschi, E. M., Rimoldi, V., Menegatti, M., Peyvandi, F., Salomon, O. & Duga, S., Jul 27 2017, In : Blood. 130, 4, p. e1-e6

Research output: Contribution to journalArticle

Exploring the global landscape of genetic variation in coagulation factor XI deficiency

Asselta, R., Paraboschi, E. M., Rimoldi, V., Menegatti, M., Peyvandi, F., Salomon, O. & Duga, S., Jul 27 2017, In : Blood. 130, 4, p. e1-e6

Research output: Contribution to journalArticle

Genome editing of factor X in zebrafish reveals unexpected tolerance of severe defects in the common pathway

Hu, Z., Liu, Y., Huarng, M. C., Menegatti, M., Reyon, D., Rost, M. S., Norris, Z. G., Richter, C. E., Stapleton, A. N., Chi, N. C., Peyvandi, F., Joung, J. K. & Shavit, J. A., Aug 3 2017, In : Blood. 130, 5, p. 666-676 11 p.

Research output: Contribution to journalArticle

Molecular investigation of 41 patients affected by coagulation factor XI deficiency

Rimoldi, V., Paraboschi, E. M., Menegatti, M., Peyvandi, F., Salomon, O., Duga, S. & Asselta, R., 2017, In : Haemophilia.

Research output: Contribution to journalArticle

Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories

Jennings, I., Kitchen, S., Menegatti, M., Palla, R., Walker, I., Peyvandi, F. & Makris, M., 2017, In : International Journal of Laboratory Hematology. 39, 6, p. 653-662

Research output: Contribution to journalArticle

2016

Disseminated intravascular coagulation with positive D-dimer: A controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran

Naderi, M., Tabibian, S., Menegatti, M., Kalantar, E., Kazemi, A., Zaker, F. & Dorgalaleh, A., Nov 13 2016, In : Blood Coagulation and Fibrinolysis. 27, 8, p. 933-935 3 p.

Research output: Contribution to journalArticle

Reduced fibrinolytic resistance in patients with factor XI deficiency. Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathway

Colucci, M., Incampo, F., Cannavò, A., Menegatti, M., Siboni, S. M., Zaccaria, F., Semeraro, N. & Peyvandi, F., Aug 1 2016, In : Journal of Thrombosis and Haemostasis. 14, 8, p. 1603-1614 12 p.

Research output: Contribution to journalArticle

2015

Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency

Asselta, R., Platè, M., Robusto, M., Borhany, M., Guella, I., Soldà, G., Afrasiabi, A., Menegatti, M., Shamsi, T., Peyvandi, F. & Duga, S., 2015, In : Thrombosis and Haemostasis. 113, 3, p. 567-576 10 p.

Research output: Contribution to journalArticle

Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency

Epcacan, S., Menegatti, M., Akbayram, S., Cairo, A., Peyvandi, F. & Oner, A. F., Oct 1 2015, In : European Journal of Clinical Investigation. 45, 10, p. 1087-1091 5 p.

Research output: Contribution to journalArticle

Neonatal onset of congenital factor X deficiency: A description of two novel mutations with 6-year follow-up

Corsini, I., Menegatti, M., Cairo, A. & Dani, C., Sep 1 2015, In : Blood Coagulation and Fibrinolysis. 26, 6, p. 679-681 3 p.

Research output: Contribution to journalArticle

Rare Inherited Coagulation Disorders

Peyvandi, F. & Menegatti, M., Nov 6 2015, Postgraduate Haematology: Seventh Edition. Wiley Blackwell, p. 733-742 10 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

2014

A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking

Menegatti, M., Vangone, A., Palla, R., Milano, G., Cavallo, L., Oliva, R., De Cristofaro, R. & Peyvandi, F., Mar 2014, In : Thrombosis Research. 133, 3, p. 481-487 7 p.

Research output: Contribution to journalArticle

Genotype and phenotype report on patients with combined deficiency of factor v and factor VIII in Iran

Karimi, M., Cairo, A., Safarpour, M. M., Haghpanah, S., Ekramzadeh, M., Afrasiabi, A., Shahriari, M. & Menegatti, M., 2014, In : Blood Coagulation and Fibrinolysis. 25, 4, p. 360-363 4 p.

Research output: Contribution to journalArticle

Thrombin generation in patients with idiopathic sudden sensorineural hearing loss

Tripodi, A., Capaccio, P., Pignataro, L., Chantarangkul, V., Menegatti, M., Bamonti, F., Clerici, M., De Giuseppe, R. & Peyvandi, F., 2014, In : Thrombosis Research. 133, 6, p. 1130-1134 5 p.

Research output: Contribution to journalArticle

2013
2012

Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran

Eshghi, P., Cohan, N., Lak, M., Naderi, M., Peyvandi, F., Menegatti, M. & Karimi, M., Jan 2012, In : Clinical and Applied Thrombosis/Hemostasis. 18, 1, p. 100-103 4 p.

Research output: Contribution to journalArticle

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: Results from the European Network of Rare Bleeding Disorders

Peyvandi, F., Palla, R., Menegatti, M., Siboni, S. M., Halimeh, S., Faeser, B., Pergantou, H., Platokouki, H., Giangrande, P., Peerlinck, K., Celkan, T., Ozdemir, N., Bidlingmaier, C., Ingerslev, J., Giansily-Blaizot, M., Schved, J. F., Gilmore, R., Gadisseur, A., Benedik-Dolničar, M., Kitanovski, L. & 3 others, Mikovic, D., Musallam, K. M. & Rosendaal, F. R., Apr 2012, In : Journal of Thrombosis and Haemostasis. 10, 4, p. 615-621 7 p.

Research output: Contribution to journalArticle

Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran

Karimi, M., Vafafar, A., Haghpanah, S., Payandeh, M., Eshghi, P., Hoofar, H., Afrasiabi, A., Gerdabi, J., Ardeshiri, R., Menegatti, M. & Peyvandi, F., Mar 2012, In : Haemophilia. 18, 2, p. 211-215 5 p.

Research output: Contribution to journalArticle

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

Lotta, L. A., Wang, M., Yu, J., Martinelli, I., Yu, F., Passamonti, S. M., Consonni, D., Pappalardo, E., Menegatti, M., Scherer, S. E., Lewis, L. L., Akbar, H., Wu, Y., Bainbridge, M. N., Muzny, D. M., Mannucci, P. M., Gibbs, R. A. & Peyvandi, F., 2012, In : BMC Medical Genomics. 5, 7.

Research output: Contribution to journalArticle

Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disorders

Van Geffen, M., Menegatti, M., Loof, A., Lap, P., Karimi, M., Laros-van Gorkom, B. A. P., Brons, P. & Van Heerde, W. L., Jul 2012, In : Haemophilia. 18, 4, p. 630-638 9 p.

Research output: Contribution to journalArticle

2011

Post-partum hemorrhage in women with rare bleeding disorders

Peyvandi, F., Menegatti, M. & Siboni, S. M., Feb 2011, In : Thrombosis Research. 127, SUPPL. 3

Research output: Contribution to journalArticle

2010

Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis

Martinelli, I., Bucciarelli, P., De Stefano, V., Passamonti, S. M., Menegatti, M., Tormene, D., Tosetto, A. & Mannucci, P. M., Dec 2010, In : European Journal of Neurology. 17, 12, p. 1482-1485 4 p.

Research output: Contribution to journalArticle

Oxidative stress is increased in primary and post-polycythemia vera myelofibrosis

Vener, C., Novembrino, C., Bamonti Catena, F., Fracchiolla, N. S., Gianelli, U., Savi, F., Radaelli, F., Fermo, E., Cortelezzi, A., Lonati, S., Menegatti, M. & Lambertenghi Deliliers, G., Nov 2010, In : Experimental Hematology. 38, 11, p. 1058-1065 8 p.

Research output: Contribution to journalArticle

Rare Bleeding Disorders

Peyvandi, F. & Menegatti, M., Nov 16 2010, Postgraduate Haematology: Sixth Edition. Wiley-Blackwell, p. 813-838 26 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

2009

Factor X deficiency

Menegatti, M. & Peyvandi, F., Jun 2009, In : Seminars in Thrombosis and Hemostasis. 35, 4, p. 407-415 9 p.

Research output: Contribution to journalArticle

2008

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

Karimi, M., Menegatti, M., Afrasiabi, A., Sarikhani, S. & Peyvandi, F., Jun 2008, In : Haematologica. 93, 6, p. 934-938 5 p.

Research output: Contribution to journalArticle

2007

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

Siboni, S. M., Spreafico, M., Menegatti, M., Martinelli, I. & Peyvandi, F., Jan 2007, In : Blood Coagulation and Fibrinolysis. 18, 1, p. 81-84 4 p.

Research output: Contribution to journalArticle

2006

Genetic diagnosis of haemophilia and other inherited bleeding disorders

Peyvandi, F., Jayandharan, G., Chandy, M., Srivastava, A., Nakaya, S. M., Johnson, M. J., Thompson, A. R., Goodeve, A., Garagiola, I., Lavoretano, S., Menegatti, M., Palla, R., Spreafico, M., Tagliabue, L., Asselta, R., Duga, S. & Mannucci, P. M., Jul 2006, In : Haemophilia. 12, SUPPL. 3, p. 82-89 8 p.

Research output: Contribution to journalArticle

Rare bleeding disorders

Peyvandi, F., Kaufman, R. J., Seligsohn, U., Salomon, O., Boltoon-Maggs, P. H. B., Spreafico, M., Menegatti, M., Palla, R., Siboni, S. & Mannucci, P. M., Jul 2006, In : Haemophilia. 12, SUPPL. 3, p. 137-142 6 p.

Research output: Contribution to journalArticle

2005

Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations [12]

Tripodi, A., Chantarangkul, V., Menegatti, M., Tagliabue, L. & Peyvandi, F., 2005, In : Clinical Chemistry. 51, 7, p. 1310-1311 2 p.

Research output: Contribution to journalArticle

2004

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, P. M., Jan 2004, In : Human Mutation. 23, 1, p. 98 1 p.

Research output: Contribution to journalArticle

2003

No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age

Mannucci, P. M., Merlini, P. A., Ardissino, D., Barzuini, C., Bernardi, F., Bernardinelli, L., Cavallini, C., Celli, P., Corsini, G., Ferrario, M., Fetiveau, R., Galli, M., Piazza, A., Ribichini, F., Sacchi, E., Tubaro, M., Zonzin, P., Berzuini, C., Foco, L., Tagliabue, L. & 79 others, Menegatti, M., Peyvandi, F., Repetto, A., Canosi, U., Cucci, V., Buratti, S., Fondazione, S., Ponzetta, M., Rinuncini, M., Spolverato, M., Vetrano, A., Lamponi, M., Cacciavillani, L., Castelli, C., Colizzi, A., Pagnoni, N., Colombi, E., Covini, D., Fantini, G., Dodi, C., Paoloni, P., Maoddi, I., Bardelli, G., Azzarito, M., Beciani, M., Tettamanti, F., Caccia, M. E., Massoli, P., Pozzi, R., Pecchio, F., Barberis, P., Giudice, M., Di Giovanbattista, R., Mazzocco, B., Gaeta, G., Margaglione, M., Diotallevi, P., Salvioni, A., Biancoli, S., Rosi, A., Milanesi, E., Span, S., Saccà, A. C. M., Maugeri, A. C., Scorzoni, D., Maffi, M., Dei Tos, G. A., Cannarozzo, P. P., Vandelli, R., Fici, M., Tempesta, A., Lucchi, G. R., Ricci, G., Baragli, D., Laiso, D., Garzaro, L., Vaninetti, R., Cattadori, G., Picozzi, A., Petacchi, R., Berardi, C., Guiducci, V., Gaddi, O., Franco, N., Buia, E., Fedeli, F., Barillà, F., Irace, L., Sarracino, S., De Giorgio, N., Scalera, G., Elia, M., Sabella, P., Previtera, A., Di Tano, G., Francaviglia, B., Contini, G., Del Nevo, F. & Agricola, P., Mar 4 2003, In : Circulation. 107, 8, p. 1117-1122 6 p.

Research output: Contribution to journalArticle

2002

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, D. J., Perkins, S. J. & Mannucci, P. M., 2002, In : British Journal of Haematology. 117, 3, p. 685-692 8 p.

Research output: Contribution to journalArticle

2001
1999

Effect of adenosine derivatives on in vitro thrombus formation induced by shear stress

Menegatti, M., Cristalli, G., Gallo, L., Mannucci, P. M. & Pareti, F. I., Aug 1999, In : Haematologica. 84, 8, p. 721-725 5 p.

Research output: Contribution to journalArticle