.. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing. Blood 2000; 96(7):2501-5
2000-01-01 Margaglione, M; Santacroce, R; Colaizzo, D; Seripa, D; Vecchione, G; Lupone, Mr; De Lucia, D; Fortina, P; Grandone, E; Perricone, C; Di Minno, G
Correlation between factors involved in the local haemostasis and angiogenesis in full term human placenta
2008-01-01 Chinni, E; Colaizzo, D; Margaglione, M; Rubini, C; D'Ambrosio, Rl; Giuliani, F; Di, ; Vagno, G; Grandone, E
Markers of haemostasis and angiogenesis in placentae from gestational vascular complications: impairment of mechanisms involved in maintaining intervillous blood flow
2010-01-01 Chinni, E; Colaizzo, D; Tiscia, Gl; Martinelli, P; Maruotti, Gm; Matteo, M; Margaglione, M; Grandone, E
.Polymorphism of the angiotensin-converting enzyme gene in end-stage renal failure patients. Nephron 2000; 85(1):54-9
2000-01-01 Aucella, F; Vigilante, M; Margaglione, M; Grandone, E; del Popolo, A; Forcella, M; Procaccini, D; Salatino, G; Passione, A; Ktena, M; De Min, A; Stallone, C
Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke. An Italian case-control study. Stroke 29:399-403; 1998
1998-01-01 Margaglione, M; Seripa, D; Gravina, C; Grandone, E; Vecchione, G; Cappucci, G; Merla, G; Papa, S; Postiglione, A; Di Minno, G; Fazio, Vm
Recurrent thrombocytopenia in pregnancy: is it always an obstetric complication?
2019-01-01 Ostuni, A; Favuzzi, G; Battista, C; Tullo, A; Cappucci, F; Makatsariya, A; Tiscia GL, ; Grandone, E
Infectious agents including COVID-19 and the involvement of blood coagulation and fibrinolysis. A narrative review
2021-01-01 Marongiu, F; Grandone, E; Scano, A; Orrù, G; Marongiu, S; Gerosa, C; Fanni, D; Faa, G; Barcellona, D.
Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome
2008-01-01 Colaizzo, D; Amitrano, L; Tiscia, Gl; Iannaccone, L; Gallone, A; Grandone, E; Guardascione, Ma; Margaglione, M
The G20210A prothrombin variant and the risk of venous thromboembolism or fetal loss in pregnant women: a family study
2007-01-01 Tormene, D; DE STEFANO, V; Grandone, E; Za, T; Perlati, M; Rossi, E; Margaglione, M; Simioni, P
. FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile. Thromb Haemost. 2002; 87(1):32-6.
2002-01-01 Margaglione, M; Bossone, A; Colaizzo, D; D'Andrea, G; Brancaccio, V; Ciampa, A; Grandone, E; Di Minno, G
Role of cytochrome P4502D6 functional polymorphisms in the efficacy of donepezil in patients with Alzheimer's disease
2011-01-01 Seripa, D; Bizzarro, A; Pilotto, A; D onofrio, G; Vecchione, G; Gallo, Ap; Cascavilla, L; Paris, F; Grandone, E; Mecocci, P; Santini, Sa; Masullo, C; Pilotto, A
. Maternal and fetal inherited thrombophilias. Am J Obstet Gynecol. 2002; 186(6):1376
2002-01-01 Grandone, E; Margaglione, M
. The Methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutations. Thromb Haemost 1998; 79:907-911
1998-01-01 Margaglione, M; D’Andrea, G; D’Addedda, M; Giuliani, N; Cappucci, G; Iannaccone, L; Vecchione, G; Grandone, E; Brancaccio, V; Di Minno, G
The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis
2007-01-01 Colaizzo, D; Amitrano, L; Tiscia, Gl; Scenna, G; Grandone, E; Guardascione, Ma; Brancaccio, V; Margaglione, M
Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations. Blood Transfus. 2018 Oct 8:1-8. doi: 10.2450/2018.0123-18
2019-01-01 Chinni, E; Tiscia, G; Favuzzi, G; Cappucci, F; Malcangi, G; Bagna, R; Izzi, C; Rizzi, D; De Stefano, V; Grandone, E
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997; 77: 1052-1054
1997-01-01 Grandone, E; Margaglione, M; Colaizzo, D; Cappucci, G; Paladini, D; Martinelli, P; Montanaro, S; Pavone, G; Di Minno, G
.Hyperhomocysteinaemia in chronic liver diseases: role of disease stage, vitamin status and methylenetetrahydrofolate reductase genetics. Liver Int. 25(1):49-56; 2005
2005-01-01 Ventura, P; Rosa, Mc; Abbati, G; Marchini, S; Grandone, E; Vergura, P; Tremosini, S; Zeneroliml,
. Occurrence of factor V Leiden mutation (Arg506Gln) and anticardiolipin antibodies in migraine patients. Neurol Sci , 2002; 22(6):455-8
2002-01-01 Intiso, D; Crociani, P; Fogli, D; Grandone, E; Cappucci, G; Di Rienzo, F; Di Viesti, P; Simone, P; Tonali, P
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions
2008-01-01 D'Andrea, G; Bafunno, V; DEL VECCHIO, L; Amoriello, A; Morabito, P; Vecchione, G; Grandone, E; Margaglione, M
.Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group. Blood Coagul Fibrinolysis. 2006; 17(4):235-40
2006-01-01 Santacroce, R; Cappucci, F; Pisanelli, D; Perricone, F; Papa, Ml; Santoro, R; Grandone, E; Margaglione, M
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