Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Silvia Vettore"'
Autor:
Fabrizio Vianello, Silvia Vettore, Fabiana Tezza, Luca De Toni, Raffaella Scandellari, Luisa Sambado, Martina Treleani, Fabrizio Fabris
Publikováno v:
Hematology Reports, Vol 6, Iss 1 (2014)
The relationship between thrombopoietin (TPO) and its receptor cMpl in thrombocytopenic conditions has not been entirely clarified. To elucidate this interplay may expand the spectrum of indications of TPO mimetics. In this study we have explored the
Externí odkaz:
https://doaj.org/article/3aa48602215a47a4b754fd9dfb74d09d
Autor:
Silvia Vettore, Fabiana Tezza, Alessandro Malara, Fabrizio Vianello, Alessandro Pecci, Raffaella Scandellari, Matteo Floris, Alessandra Balduini, Fabrizio Fabris
Publikováno v:
Haematologica, Vol 96, Iss 12 (2011)
Platelet glycoprotein GPIbα mutations are the basic defect behind Bernard-Soulier syndrome, a rare inherited macrothrombocytopenia characterized by anomalies of the GPIbα, GPIbβ and GPIX subunits of von Willebrand factor receptor. A 32-year old ma
Externí odkaz:
https://doaj.org/article/cc2cab7b71ee4617afb8147033b544b0
Autor:
Silvia Vettore, Raffaella Scandellari, Stefano Moro, Anna Maria Lombardi, Margherita Scapin, Maria Luigia Randi, Fabrizio Fabris
Publikováno v:
Haematologica, Vol 93, Iss 11 (2008)
In Italy, a significant proportion of patients with autosomal dominant inheritance of macrothrombocytopenia have been recognized as having heterozygous Bernard-Soulier syndrome carrying the Bolzano-type defect. This condition prompted a systematic re
Externí odkaz:
https://doaj.org/article/a32f654ec43b47829185739e6266971a
Platelets express and release osteocalcin and co‐localize in human calcified atherosclerotic plaques
Autor:
Giacomo Strapazzon, Andrea Garolla, F. Grego, Silvia Vettore, Carlo Foresta, Fabrizio Fabris, Gino Gerosa, L. De Toni
Publikováno v:
Journal of Thrombosis and Haemostasis. 11:357-365
Summary. Background: Although vascular-calcification mechanisms are only partially understood, the role of circulating calcifying cells and non-collagenous bone matrix proteins in the bone–vascular axis is emerging. In spite of the fact that platel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399a663aeed794b6049d9ce195f928fd
https://doi.org/10.1111/jth.12088
https://doi.org/10.1111/jth.12088
Publikováno v:
Blood Coagulation & Fibrinolysis. 24:18-22
Patients with a low platelet count are prone to bleeding. The occurrence of a thrombotic event in congenital thrombocytopenic patients is rare and puzzling. At least nine patients with Glanzmann thrombasthenia have been reported to have had a thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1077824b23c983e730c764b1ca397999
https://doi.org/10.1097/mbc.0b013e3283597634
https://doi.org/10.1097/mbc.0b013e3283597634
Autor:
Mirto Foletto, Marnie Granzotto, Veronica Zanato, Anna M. Lombardi, Maria T. Sartori, Silvia Vettore, Roberto Vettor, Alessandro Scarda, Pamela Scarparo, Mario Plebani, Giulia Berti de Marinis, Roberto M. Serra, Roberto Fabris, Chiara Dal Pra, Fabrizio Fabris
Publikováno v:
European Journal of Clinical Investigation. 42:1197-1204
Eur J Clin Invest 2012; 42 (11): 1197–1204 Abstract Background The low-grade chronic inflammation present in obesity has been recognized as a risk factor for thrombosis, atherosclerosis and cardiovascular complications. In this context, production
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a8637fd3b41beca6c0c26fed0d7a18b
https://doi.org/10.1111/j.1365-2362.2012.02710.x
https://doi.org/10.1111/j.1365-2362.2012.02710.x
Autor:
Giulia Berti de Marinis, Martina Treleani, Silvia Vettore, Antonio Girolami, Emanuela Bonamigo
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 19:613-618
Immunological thrombocytopenias, as other forms of thrombocytopenia, are associated with bleeding. Occasionally, these patients manifest thrombotic events. A total of at least 29 patients were reported to have had either arterial (20 cases) or venous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50194d123b0456d2dab7c5f8db92ea7d
https://doi.org/10.1177/1076029612452114
https://doi.org/10.1177/1076029612452114
Autor:
Fabrizio Fabris, Silvia Vettore, Fabrizio Vianello, Giulia Berti de Marinis, Antonio Girolami
Publikováno v:
Journal of Thrombosis and Thrombolysis. 34:513-517
Bernard-Soulier Syndrome is characterized by thrombocytopenia with large platelets and defective aggregation to ristocetin. The bleeding tendency is variable but may be severe. The syndrome is due to genetic defects of the GPIb-V-IX complex and it ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ecc2b9bb324fb62291cd5459122934b
https://doi.org/10.1007/s11239-012-0742-6
https://doi.org/10.1007/s11239-012-0742-6
Autor:
Fabrizio Vianello, Silvia Vettore, Raffaella Scandellari, Alessandro Pecci, Fabrizio Fabris, Alessandra Balduini, Matteo Floris, Fabiana Tezza, Alessandro Malara
Publikováno v:
Haematologica. 96:1878-1882
Platelet glycoprotein GPIbα mutations are the basic defect behind Bernard-Soulier syndrome, a rare inherited macrothrombocytopenia characterized by anomalies of the GPIbα, GPIbβ and GPIX subunits of von Willebrand factor receptor. A 32-year old ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4280153c56dc3f7cdc01e455bf54918
https://doi.org/10.3324/haematol.2010.039008
https://doi.org/10.3324/haematol.2010.039008
Autor:
Antonio Girolami, Elisabetta Ruzzon, Silvia Vettore, Fabrizio Fabris, Giulia Berti de Marinis
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 18:121-127
Epistaxis, superficial and deep hematomas, hemarthrosis, gastrointestinal bleeding, hematuria represent the most frequent hemorrhagic events in congenital coagulation disorders. Occasionally, bleeding manifestations occur in unusual sites or are pecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53d70f8ae70085f255a4cf1bf4397c1
https://doi.org/10.1177/1076029611416638
https://doi.org/10.1177/1076029611416638