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Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia

Bone marrow transplantation (Basingstoke), 2014-11, Vol.49 (11), p.1376-1381

2014

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Pathogenesis of chronic rhinosinusitis in patients affected by β-thalassemia major and sickle cell anaemia post allogenic bone marrow transplant

International journal of pediatric otorhinolaryngology, 2018-03, Vol.106, p.35-40

2018

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Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of hematopoietic SCT in sickle cell anemia

Bone marrow transplantation (Basingstoke), 2012-02, Vol.47 (2), p.227-230

2012

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Higher CD3 and CD34 cell doses in the graft increase the incidence of acute GVHD in children receiving BMT for thalassemia

Bone marrow transplantation (Basingstoke), 2012-01, Vol.47 (1), p.107-114

2012

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Second hematopoietic SCT in patients with thalassemia recurrence following rejection of the first graft

Bone marrow transplantation (Basingstoke), 2008-09, Vol.42 (6), p.397-404

2008

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G20210A Prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects

British heart journal, 2004-01, Vol.90 (1), p.82-86

2004

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Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease

European heart journal, 2002-01, Vol.23 (1), p.26-30

2002

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The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

The New England journal of medicine, 1999-09, Vol.341 (11), p.801-806

1999

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Screening for inherited thrombophilia: indications and therapeutic implications

Haematologica (Roma), 2002-10, Vol.87 (10), p.1095

2002

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Recurrent deep vein thrombosis after the insertion of two vascular accesses in a 13-year-old thalassemic girl waiting for a haploidentical marrow transplant

The journal of vascular access, 2009-01, Vol.10 (1), p.64-65

2009

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Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium

Thrombosis and haemostasis, 2002-05, Vol.87 (5), p.791-795

2002

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Prevalence of the C536T mutation in the tissue factor pathway inhibitor (TFPI) gene among patients with venous thromboembolic disease

Thrombosis and haemostasis, 2001-05, Vol.85 (5), p.938-939

2001

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Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families

Blood, 1998-10, Vol.92 (7), p.2353-2358

1998

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Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease

Blood coagulation & fibrinolysis, 2000-07, Vol.11 (5), p.499-503

2000

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Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia

Thrombosis and haemostasis, 1998-08, Vol.80 (2), p.342-343

1998

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G20210A prothrombin gene polymorphism and extent of coronary disease

Thrombosis and haemostasis, 2000-07, Vol.84 (1), p.142-143

2000

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807CC genotype of the platelet Gp Ia could represent a protective factor for recurrences of acute coronary events in acute coronary syndromes

Journal of the American College of Cardiology, 2002-03, Vol.39, p.310-310

2002

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Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients

Blood, 1998-05, Vol.91 (10), p.3562-3565

1998

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Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients

Blood, 1998-05, Vol.91 (10), p.3562-3565

1998

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Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease

Thrombosis and haemostasis, 1998-03, Vol.79 (3), p.686-687

1998

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Epidemiology of Factor V Leiden: Clinical Implications

Seminars in thrombosis and hemostasis, 1998-01, Vol.24 (4), p.367-379

1998

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Cerebral vein thrombosis not related to use of oral contraceptives in a 7-year-old child carrier of the prothrombin 20210A allele

Thrombosis and haemostasis, 1999-06, Vol.81 (6), p.991-992

1999

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Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele

Thrombosis and haemostasis, 1998-09, Vol.80 (3), p.519-519

1998

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Thrombotic risk during pregnancy and puerperium in women with APC-resistance--effective subcutaneous heparin prophylaxis in a pregnant patient

Thrombosis and haemostasis, 1995, Vol.74 (2), p.793-794

1995

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The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation

British journal of haematology, 2001-06, Vol.113 (3), p.630-635

2001

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Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia

Pathogenesis of chronic rhinosinusitis in patients affected by β-thalassemia major and sickle cell anaemia post allogenic bone marrow transplant

Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of hematopoietic SCT in sickle cell anemia

Higher CD3 and CD34 cell doses in the graft increase the incidence of acute GVHD in children receiving BMT for thalassemia

Second hematopoietic SCT in patients with thalassemia recurrence following rejection of the first graft

G20210A Prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects

Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease

The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

Screening for inherited thrombophilia: indications and therapeutic implications

Recurrent deep vein thrombosis after the insertion of two vascular accesses in a 13-year-old thalassemic girl waiting for a haploidentical marrow transplant

Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium

Prevalence of the C536T mutation in the tissue factor pathway inhibitor (TFPI) gene among patients with venous thromboembolic disease

Different Risks of Thrombosis in Four Coagulation Defects Associated With Inherited Thrombophilia: A Study of 150 Families

Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease

Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia

G20210A prothrombin gene polymorphism and extent of coronary disease

807CC genotype of the platelet Gp Ia could represent a protective factor for recurrences of acute coronary events in acute coronary syndromes

Prothrombin G20210A Mutant Genotype Is a Risk Factor for Cerebrovascular Ischemic Disease in Young Patients

Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients

Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease

Epidemiology of Factor V Leiden: Clinical Implications

Cerebral vein thrombosis not related to use of oral contraceptives in a 7-year-old child carrier of the prothrombin 20210A allele

Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele

Thrombotic risk during pregnancy and puerperium in women with APC-resistance--effective subcutaneous heparin prophylaxis in a pregnant patient

The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation

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