S. Vettore

发表

Serum Thrombopoietin and cMpl Expression in Thrombocytopenia of Different Etiologies

F. Fabris, F. Vianello, S. Vettore, 2014, Hematology reports.

Arterial and venous thrombosis in patients with von Willebrand’s disease: A critical review of the literature

A. Girolami, S. Vettore, F. Tezza, 2006, Journal of Thrombosis and Thrombolysis.

Rare and Unusual Bleeding Manifestations in Congenital Bleeding Disorders

F. Fabris, A. Girolami, S. Vettore, 2012, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Conformational Changes of Congenital FVII Variants with Defective Binding to Tissue Factor ARG304GLN (FVII Padua), ARG 304TRP (FVII Nagoya) and ARG79GLN (FVII Shinjo or Tondabayashi)

S. Moro, A. Girolami, A. Bulfone, 2013, International journal of biomedical science : IJBS.

Determinants of plasma levels of plasminogen activator inhibitor-1 : A study of normotensive twins.

S. Vettore, G. Patrassi, M. Sartori, 1999, Arteriosclerosis, thrombosis, and vascular biology.

4G/5G Polymorphism of PAI-1 Gene Promoter and Fibrinolytic Capacity in Patients with Deep Vein Thrombosis

B. Wiman, A. Girolami, F. Dazzi, 1998, Thrombosis and Haemostasis.

Identification of an 18 basepair deletion in the PAI-1 gene promoter region in a family with thrombotic disease

B. Wiman, A. Girolami, S. Vettore, 1997 .

Platelet response to Helicobacter pylori eradication therapy in adult chronic idiopathic thrombocytopenic purpura seems to be related to the presence of anticytotoxin-associated gene A antibodies

F. Fabris, M. Plebani, E. Allemand, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review

A. Girolami, B. Girolami, S. Vettore, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature

A. Girolami, B. Girolami, S. Vettore, 2009, Journal of Thrombosis and Thrombolysis.

The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency

A. Lombardi, A. Girolami, B. Girolami, 2010, Journal of Thrombosis and Thrombolysis.

About the rarity of haemoptysis in congenital bleeding disorders. A report of five cases (1)

A. Girolami, E. Allemand, B. Girolami, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Congenital FVII Deficiency and Pulmonary Embolism

A. Girolami, B. Girolami, S. Vettore, 2013, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Arterial and Venous Thromboses in Patients With Idiopathic (Immunological) Thrombocytopenia

A. Girolami, S. Vettore, M. Treleani, 2013, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard–Soulier syndrome

F. Fabris, A. Girolami, F. Vianello, 2012, Journal of Thrombosis and Thrombolysis.

Congenital FVII deficiency and thrombotic events after replacement therapy

A. Girolami, S. Vettore, R. Muzzolon, 2011, Journal of Thrombosis and Thrombolysis.

Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes).

F. Fabris, A. Girolami, S. Vettore, 2011, Journal of thrombosis and thrombolysis.

Congenital bleeding disorders of the vitamin K-dependent clotting factors.

A. Girolami, S. Vettore, R. Scandellari, 2008, Vitamins and hormones.

Impairment of fibrinolytic potential in long-term steroid treatment after heart transplantation.

A. Girolami, S. Vettore, U. Livi, 1997, Transplantation.

1α,25-Dihydroxyvitamin D3 inhibits the human H295R cell proliferation by cell cycle arrest: A model for a protective role of vitamin D receptor against adrenocortical cancer

H. Sasano, A. Fassina, P. Mulatero, 2014, The Journal of Steroid Biochemistry and Molecular Biology.

Discrepancies between clotting and chromogenic assays in congenital coagulation disorders: the hemostatic coin has only one face, chromogenic substrates many.

A. Girolami, S. Vettore, 2009, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect.

F. Fabris, A. Savoia, C. Balduini, 2010, European journal of medical genetics.

Different genotypes are responsible for the normal Russell viper venom assays seen in some cases of congenital factor X deficiency

A. Girolami, S. Vettore, M. Scapin, 2008, American journal of hematology.

Subunit change in cytochrome c oxidase: identification of the oxygen switch in Dictyostelium

S. Vettore, D. Sandonà, R. Bisson, 1997, The EMBO journal.

Clinical biological remission induced by rituximab in acute refractory chronic relapsing TTP.

A. Lombardi, F. Fabris, P. Sansoni, 2010, Thrombosis research.

Neurofilament M mRNA is expressed in conduction system myocytes of the developing and adult rabbit heart.

K. Chien, S. Vettore, M. Vitadello, 1996, Journal of molecular and cellular cardiology.

Regional and age-related differences in mRNA composition of intracellular Ca(2+)-release channels of rat cardiac myocytes.

V. Sorrentino, S. Vettore, M. Vitadello, 1997, Journal of molecular and cellular cardiology.

Molecular and cellular diversity of heart conduction system myocytes.

S. Vettore, M. Vitadello, L. Gorza, 1994, Trends in cardiovascular medicine.

Congenital Combined Defects of Factor VII: A Critical Review

A. Girolami, E. Allemand, S. Vettore, 2006, Acta Haematologica.

Presence of anti‐ADAMTS13 antibodies in obesity

F. Fabris, M. Plebani, R. Vettor, 2012, European journal of clinical investigation.

Occurrence of thrombosis in congenital thrombocytopenic disorders: a critical annotation of the literature

A. Lombardi, A. Girolami, S. Vettore, 2013, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Cardiac Myocytes Differ in mRNA Composition for Sarcoplasmic Reticulum Ca2+ Channels and Ca2+ Pumpsa a

A. Lompré, P. Volpe, S. Vettore, 1995, Annals of the New York Academy of Sciences.

Novel point mutation in a leucine-rich repeat of the GPIbα chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant

S. Moro, A. Lombardi, F. Fabris, 2008, Haematologica.

Confirmation of the Value of a Modified Long-distance Polymerase Chain Reaction in the Detection of Inversion Intron 22 in Severe Hemophilia A: A Technical Note

A. Lombardi, A. Girolami, E. Zanon, 2005, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia

F. Fabris, N. Bizzaro, S. Vettore, 2010, Thrombosis and Haemostasis.

The association of a mild FXII deficiency with myocardial infarction and venous thrombosis is completely unjustified

A. Girolami, S. Vettore, P. Scarparo, 2009, Journal of Thrombosis and Thrombolysis.

About the significance or the insignificance of the factor XII C46T polymorphism: a rebuttal

A. Lombardi, A. Girolami, S. Vettore, 2007, Journal of thrombosis and haemostasis : JTH.

A large family from Argentina with Prekallikrein deficiency due to a compound heterozygosis (T insertion in intron 7 and Asp558Glu in exon 15): Prekallikrein Cordoba

A. Lombardi, A. Girolami, A. Tabares, 2010, American journal of hematology.

Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era

A. Lombardi, A. Girolami, S. Vettore, 2011, Haemophilia : the official journal of the World Federation of Hemophilia.

A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis

A. Balduini, F. Fabris, A. Pecci, 2011, Haematologica.

A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbα gene: Lack of GPIbα but absence of bleeding

A. Lombardi, F. Fabris, S. Vettore, 2008, Platelets.

Retinal central artery occlusion in a young woman after ten days of a drospirenone-containing oral contraceptive (Yasmin)

A. Girolami, B. Girolami, S. Vettore, 2007, Thrombosis and Haemostasis.

Mild factor VII deficiency due to heterozygosis is not associated with a bleeding tendency.

A. Girolami, E. Zanon, S. Vettore, 2005, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A. Girolami, S. Vettore, E. Bonamigo, 2011, Laboratory hematology : official publication of the International Society for Laboratory Hematology.

Unexplained Discrepancies in the Activity—Antigen Ratio in Congenital FX Deficiencies With Defects in the Catalytic Domain

A. Lombardi, A. Girolami, S. Vettore, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Platelets express and release osteocalcin and co‐localize in human calcified atherosclerotic plaques

G. Gerosa, G. Strapazzon, C. Foresta, 2013, Journal of thrombosis and haemostasis : JTH.

Ox Brain versus Rabbit Brain Thromboplastin Assays Are the Best Tool for a Preliminary Diagnosis of the Arg304Gln Factor VII Defect (FVII Padua)

A. Girolami, R. Sartori, S. Vettore, 2010, Acta Haematologica.

Different fatherhood as a possible explanation for difficult pedigrees in coagulation defects: only ‘mater semper certa est’

A. Lombardi, A. Girolami, S. Vettore, 2005, British journal of haematology.

The lack of ties between north-eastern Italy and African-Americans suggest a multi-founder effect for FVII Padua (Arg304Gln) disorder.

A. Girolami, S. Vettore, E. Bonamigo, 2010, Blood Coagulation and Fibrinolysis.