Patrizia Noris

Pavia, Italy

Last Updated: 09/26/2026

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Found 61 publications

Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: Back to the clinical phenotype.

Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: Back to the clinical phenotype.

Journal: HemaSphere
Published: September 10, 2024

Association of human leucocyte antigen loci with vaccine-induced immune thrombotic thrombocytopenia: Potential role of the interaction between platelet factor 4-derived peptides and MHC-II.

Association of human leucocyte antigen loci with vaccine-induced immune thrombotic thrombocytopenia: Potential role of the interaction between platelet factor 4-derived peptides and MHC-II.

Journal: British journal of haematology
Published: August 05, 2024

Isolated thrombocytopenia in pregnancy: A monocentric retrospective study of 63 pregnancies in 59 women.

Isolated thrombocytopenia in pregnancy: A monocentric retrospective study of 63 pregnancies in 59 women.

Journal: EJHaem
Published: May 10, 2024

GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.

GP1BB c.179C > T is the most frequent cause of monoallelic Bernard-Soulier syndrome in the Italian population after the Bolzano variant: a report of two new families.

Journal: Annals of hematology
Published: October 21, 2022

Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup.

Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup.

Journal: Haematologica
Published: March 04, 2022

ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism.

ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism.

Journal: Haematologica
Published: February 04, 2022

Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.

Expert opinion on the use of platelet secretion assay for the diagnosis of inherited platelet function disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.

Journal: Journal of thrombosis and haemostasis : JTH
Published: February 04, 2022

A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.

A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.

Journal: International journal of molecular sciences
Published: August 19, 2021

GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme.

GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme.

Journal: Haematologica
Published: August 11, 2021

Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy.

Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy.

Journal: Internal and emergency medicine
Published: January 05, 2021

The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.

The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology.

Journal: Journal of thrombosis and haemostasis : JTH
Published: October 29, 2020

Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation.

Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel GFI1B germline mutation.

Journal: Haematologica
Published: July 31, 2020
Showing 1-12 of 61

Last Updated: 09/26/2026