List of works - Silvia Ferrari

A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).

scientific article

A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma

scientific article published on 13 May 2016

A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia.

scientific article

A structure-function analysis in patients with prekallikrein deficiency.

scientific article published on 22 November 2017

Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory Finding

scientific article published on 31 August 2015

Activated platelet-derived and leukocyte-derived circulating microparticles and the risk of thrombosis in heparin-induced thrombocytopenia: A role for pf4-bearing microparticles?

scientific article

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

scientific article

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period

scientific article published on 8 February 2017

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study.

scientific article

Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T).

scientific article published on 7 September 2017

Congenital factor XI and factor VII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: An intriguing observation

scientific article

Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.

scientific article published in August 2017

Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients

scientific article

Drug-Induced Thrombophilic or Prothrombotic States

scientific article published on 14 June 2016

Factor X Friuli Coagulation Disorder.

scientific article

Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation.

scientific article

Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported cases.

scientific article

New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice

scientific article published on March 2017

New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.

scientific article published on 12 March 2018

Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.

scientific article

Prethrombotic, prothrombotic, thrombophilic states, hypercoagulable state, thrombophilia etc.: semantics should be respected even in medical papers.

scientific article

Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).

scientific article

Prevalence of hypertension and its complications in congenital prekallikrein deficiency: analysis of all reported cases and clinical significance

scientific article published on 01 July 2015

Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis

scientific article published on 24 April 2018

Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions

scientific article published on 10 August 2017

Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected

scientific article

The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VII.

scientific article published on 14 May 2015

The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation

scientific article published on 04 August 2020

Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations

scientific article published on 7 July 2016

Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.

scientific article published in January 2017

List of works by Silvia Ferrari

A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).

A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma

A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia.

A structure-function analysis in patients with prekallikrein deficiency.

Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory Finding

Activated platelet-derived and leukocyte-derived circulating microparticles and the risk of thrombosis in heparin-induced thrombocytopenia: A role for pf4-bearing microparticles?

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study.

Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T).

Congenital factor XI and factor VII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: An intriguing observation

Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.

Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients

Drug-Induced Thrombophilic or Prothrombotic States

Factor X Friuli Coagulation Disorder.

Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation.

Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported cases.

New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice

New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.

Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.

Prethrombotic, prothrombotic, thrombophilic states, hypercoagulable state, thrombophilia etc.: semantics should be respected even in medical papers.

Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).

Prevalence of hypertension and its complications in congenital prekallikrein deficiency: analysis of all reported cases and clinical significance

Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis

Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions

Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected

The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VII.

The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation

Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations

Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.