M G Cattini
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Explore the profile of M G Cattini including associated specialties, affiliations and a list of published articles.
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12
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109
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Recent Articles
1.
Pontara E, Cheng C, Cattini M, Bison E, Pelloso M, Denas G, et al.
Lupus
. 2019 Nov;
28(14):1663-1668.
PMID: 31701800
Platelet activation and decrease in platelet count characterize the development of the most feared form of antiphospholipid syndrome (APS), i.e. catastrophic APS (CAPS). We aimed to assess if immuno-affinity purified...
2.
Pengo V, Del Ross T, Ruffatti A, Bison E, Cattini M, Pontara E, et al.
Thromb Res
. 2018 Nov;
172:172-178.
PMID: 30466070
Background: Whether antibodies directed to β2-Glycoprotein I (aβ2GPI) are responsible for LA activity is not well defined. However, in the absence of such antibodies the molecule responsible for LA phenomenon...
3.
Pontara E, Banzato A, Bison E, Cattini M, Baroni G, Denas G, et al.
J Thromb Haemost
. 2018 Jan;
16(3):529-532.
PMID: 29316193
Summary: Background Thrombocytopenia is the most common non-criteria hematological feature in patients with antiphospholipid syndrome (APS). This condition is more common in patients with catastrophic APS (CAPS). Objectives To evaluate...
4.
Daidone V, Barbon G, Cattini M, Pontara E, Romualdi C, Di Pasquale I, et al.
Haemophilia
. 2016 Jun;
22(6):949-956.
PMID: 27293213
Introduction: The heterogeneity of von Willebrand disease (VWD) makes its diagnosis a difficult task. Methods: We report here on the usefulness of a microchip-based flow-chamber system, the total thrombus-formation analysis...
5.
Casonato A, Cattini M, Barbon G, Daidone V, Pontara E
Thromb Res
. 2015 Aug;
136(3):682-6.
PMID: 26251079
Bullet Points: What is known about this topic? - Type 1 VWD is transmitted mainly as a dominant trait. - Recessive type 1 mutations at homozygous or compound heterozygous level...
6.
Koutroumpi S, Daidone V, Sartori M, Cattini M, Albiger N, Occhi G, et al.
Pituitary
. 2012 May;
16(2):175-81.
PMID: 22585010
A high incidence of venous thromboembolic (VTE) complications has been reported in Cushing's syndrome (CS), mostly post-operatively and attributable to hypercoagulability. The prevalence of symptomatic VTE was investigated retrospectively in...
7.
Sztukowska M, Gallinaro L, Cattini M, Pontara E, Sartorello F, Daidone V, et al.
Br J Haematol
. 2008 Aug;
143(1):107-14.
PMID: 18691167
Reduced von Willebrand factor (VWF) half-life has been suggested as a new pathogenic mechanism in von Willebrand disease (VWD). The usefulness of VWF propeptide (VWFpp) in exploring VWF half-life was...
8.
Casonato A, Pontara E, Sartorello F, Cattini M, Perutelli P, Bertomoro A, et al.
Clin Appl Thromb Hemost
. 2007 Apr;
13(2):194-200.
PMID: 17456630
The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling hemophilia A. Type 2N characterization is based...
9.
Casonato A, Fabris F, Pontara E, Cattini M, Zocca N, Gallinaro L, et al.
Clin Appl Thromb Hemost
. 2006 Sep;
12(3):296-304.
PMID: 16959682
Thrombotic thrombocytopenic purpura (TTP) is characterized by intravascular thrombosis leading to consumption of large or unusually large von Willebrand factor (VWF) multimers. The usefulness of VWF collagen binding (VWF:CB) assay...
10.
Casonato A, Pontara E, Doria A, Bertomoro A, Cattini M, Gambari P, et al.
Br J Haematol
. 2002 Mar;
116(4):899-904.
PMID: 11886398
We report a case of acquired von Willebrand syndrome (AVWS) in a 20-year-old-woman with systemic lupus erythematosus, in whom severe bleeding complications followed kidney biopsy. Coagulation studies demonstrated undetectable levels...