Silvia Ferrari
Padova, Italy
Last Updated: 09/26/2026
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Found 45 publications
Case Report: Hermansky-Pudlak syndrome type 1 with pulmonary involvement in a 62-year-old Caucasian woman with rheumatoid arthritis.
Journal: Frontiers in immunology
Published: December 30, 2025
Clinical and Genetic Characterization of 269 Patients With Suspected Inherited Platelet Disorders: The Padua Monocentric Experience.
Journal: International journal of laboratory hematology
Published: November 14, 2025
The compound pathogenic effects of a homozygous frameshift variant in the transmembrane region of GP9, causing Bernard-Soulier syndrome, with a missense variant in GP1BB.
Journal: British journal of haematology
Published: April 17, 2024
The Lesson Learned from the New c.2547-1G > T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect.
Journal: Thrombosis and haemostasis
Published: February 21, 2022
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
Worldwide Distribution of PK Deficiency: the Defect Seems Mainly Concentrated in West African Countries and the United States.
Journal: Mediterranean journal of hematology and infectious diseases
Published: November 25, 2020
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 novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome.
Journal: Aging clinical and experimental research
Published: July 22, 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
Last Updated: 09/26/2026