Prizes, Awards and Grants
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| 1998 | |
| Prize awarded to the best scientific communication, 15th Congress of the Italian Society for Thrombosis and Haemostasis, Naples, September 11-13. |
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| 1999 | |
| Young Investigator Award for best scientific communication, 17th Congress of the International Society on Thrombosis and Haemostasis. Washington DC, August 14-21. |
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| 2000 | |
| Prize awarded to young scientists, 16th Congress of the Italian Society Thrombosis and Hemostasis - Milan, May, 2000. |
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| 2001 | |
| Studio in vivo e in vitro del processo angiogenetico mediato da VEGF in pazienti con ischemia del miocardio (In vivo and in vitro studies of angiogenetic process by VEGF in patients by myocardial infarction). Cariplo Foundation, Milan, Italy | |
| 2001 | |
| Malattie rare della coagulazione: studio fenotipico e genotipico delle proteine dlla coagulazione (Rare coagulation disorders: phenotypic and genotypic studies on coagulation proteins). MURST, University of Milan, Italy (COFIN) |
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| 2002 | |
| Caratterizzazione molecolare dei difetti della metalloproteinasi ADAMTS 13 nelle microangiopatie trombotiche (Molecular characterization of the metalloprotease ADAMTS13 gene in thrombotic microangiopathies). IRCCS Maggiore Hospital, Milan, Italy | |
| 2003 | |
| Evaluation of gene polymorphisms associated with thrombosis and pharmocogenomic studies on anticoagulants using new high throughput techniques. IRCCS Maggiore Hospital, Milan, Italy |
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| 2003 | |
| Quantitative and functional assays of the VWF-cleaving protease (ADAMTS-13) for thrombotic thrombocytopenic purpura. Cariplo Foundation, Milan, Italy |
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| 2003 | |
| Phenotype and genotype characterization of recessively inherited coagulation disorders. Bayer Hemophilia Awards Program (early career investigator award). USA |
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| 2003 | |
| Clinical and molecular diagnosis of rare coagulation disorders. UniCredit Private Bank, Italy |
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| 2003 | |
| Bloodomics: integrated project of the European Commission 6th framework programme of research, technological development and demonstration (our Centre was involved as a collaborator group). | |
| 2003 | |
| Membrane metalloproteinases involved in disorders of haemostasis. MURST, University of Milan, Italy (COFIN) | |
| 2004 | |
| Cardiovascular disease in congenital haemorrhagic defects. University of Milan, Italy (FIRST) |
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| 2004 | |
| Inflammation genes and development of myocardial infarction at a young age. Retrospective case control study of 2000 cases and 2000 controls enrolled by 125 Italian Coronary Care Unit in eight years. Cariplo Foundation, Milan, Italy |
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| 2004 | |
| Molecular genetics of hereditary rare bleeding disorders in Indian population. Ministry of Foreign Affairs, General Directorate for Cultural Promotion and Co-operation 2004: Association between polymorphisms in gene encoding for inflammaton protein and juvenile myocardial infarction. MURST, University of Milan, Italy (COFIN) |
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| 2004 | |
| :Development of new quantitative and functional assays of the VWF-cleaving protease (ADAMTS-13) for thrombotic thrombocytopenic purpura. IRCCS Maggiore Hospital, Milan, Italy. |
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| 2005 | |
| Fetal sex determination during the first trimester of pregnancy using non-invasive techniques. Monzino Foundation, Milan, Italy |
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| 2006 | |
| Mechanisms coupling protein folding and transport at the ER-Golgi interface:role in F5F8D and other diseases San Raffaele Hospital, Milan, Italy |
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| 2006 | |
| International registry on patients affected by Thrombotic Thrombocytopenic Purpura (TTP): phenotypical and genotypical characterization. University of Milan-FIRST 2005 - www.ttpdatabase.org |
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| 2006 | |
| Trombospondine-1 (TSP-1), ADAMTS13 and von Willebrand factor(VWF): role of Thrombotic Thrombocytopenic Purpura (TTP). University of Milan-FIRST 2006 |
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| 2007 | |
| Establishment of an European Network of Rare Bleeding Disorders. Commission of the European Communities- Public Health Executive Agency (PHEA) - www.rbdd.eu |
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| 2007 | |
| Establishment of a European Network of Rare Bleeding Disorders. Istituto Superiore di Sanità, Rome - www.rbdd.eu |
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| 2005 - 2007 | |
| "Hemophilia Treatment Centre Twinning Programme " between the Hemophilia and thrombosi Centre, Maggiore Hospital and Nemazee Hospital Shiraz, Iran, awarded by WFH (World Federation of Hemophilia). | |
| 2008 | |
| Cellule fetali nel sangue materno. Una promettente tecnica non invasiva di diagnosi prenatale delle malattie genetiche. Italo Monzino Foundation, Milan - Italy 2008 Cellule fetali nel sangue materno. Una promettente tecnica non invasiva di diagnosi Menorrhagia and other gynecological problems in women affected by rare bleeding disorders. Laboratoire français du Fractionnement et des Biotechnologies (LFB) - France Determinazione del sesso fetale nel I0 trimestre di gravidanza mediante tecniche non |
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| 2011 | |
| Discovery of genetic determinants of inhibitor development in hemophilia a by exome sequencing. Bayer Hemophilia Awards Program (Special project award) |
