Antonio Girolami

A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency.

Journal: Journal of pediatric hematology/oncology

Published: April 26, 2021

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: March 03, 2021

Prevalence of Cardiovascular Disorders in African-Americans With Congenital Prekallikrein Deficiency Versus Caucasians-Americans With the Same Defect.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: November 12, 2020

An acquired prekallikrein deficiency can be diagnosed only after a sure exclusion of a congenital condition.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: August 28, 2020

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

Journal: British journal of haematology

Published: August 05, 2020

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding.

Journal: Journal of thrombosis and thrombolysis

Published: July 02, 2020

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: April 04, 2020

Long-term safety outcomes of prekallikrein (Fletcher factor) deficiency: A systematic literature review of case reports.

Journal: Allergy and asthma proceedings

Published: January 01, 2020

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.

Journal: Acta haematologica

Published: December 11, 2019

A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency.

A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency.

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Prevalence of Cardiovascular Disorders in African-Americans With Congenital Prekallikrein Deficiency Versus Caucasians-Americans With the Same Defect.

Prevalence of Cardiovascular Disorders in African-Americans With Congenital Prekallikrein Deficiency Versus Caucasians-Americans With the Same Defect.

An acquired prekallikrein deficiency can be diagnosed only after a sure exclusion of a congenital condition.

An acquired prekallikrein deficiency can be diagnosed only after a sure exclusion of a congenital condition.

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

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

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding.

A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding.

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.

Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.

Long-term safety outcomes of prekallikrein (Fletcher factor) deficiency: A systematic literature review of case reports.

Long-term safety outcomes of prekallikrein (Fletcher factor) deficiency: A systematic literature review of case reports.

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.

Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.

New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar ways.

New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar ways.

Long-term safety outcomes of prekillikrein (Fletcher factor) deficiency: A systematic literature review of case reports.

Long-term safety outcomes of prekillikrein (Fletcher factor) deficiency: A systematic literature review of case reports.

Appearance, consumer liking and preferences of Lucanian 'Soppressata' salami.

Appearance, consumer liking and preferences of Lucanian 'Soppressata' salami.