Alessandro Pecci

Pavia, Italy

Last Updated: 09/26/2026

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Found 99 publications

CHARACTERIZATION OF A SERIES OF PATIENTS WITH GNE-RELATED THROMBOCYTOPENIA: INSIGHTS INTO PATHOGENESIS, DIAGNOSIS, AND TREATMENT.

CHARACTERIZATION OF A SERIES OF PATIENTS WITH GNE-RELATED THROMBOCYTOPENIA: INSIGHTS INTO PATHOGENESIS, DIAGNOSIS, AND TREATMENT.

Journal: Journal of thrombosis and haemostasis : JTH

Published: May 23, 2026

A polygenic etiology for inherited thrombocytopenias of unknown origin.

A polygenic etiology for inherited thrombocytopenias of unknown origin.

Journal: HemaSphere

Published: March 06, 2026

Interlaboratory exercise on the use of immunofluorescence microscopy on the blood smear for recognizing inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelets in Health and Disease.

Interlaboratory exercise on the use of immunofluorescence microscopy on the blood smear for recognizing inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelets in Health and Disease.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 30, 2025

When increased bone marrow blasts may not mean malignancy.

When increased bone marrow blasts may not mean malignancy.

Journal: Blood

Published: July 10, 2025

Characterization of a novel FLI1 mutation in a family with thrombocytopenia and other congenital malformations.

Characterization of a novel FLI1 mutation in a family with thrombocytopenia and other congenital malformations.

Journal: Haematologica

Published: December 23, 2024

Microbiological diversity among patients with Lemierre syndrome and clinical implications: an individual patient-level analysis.

Microbiological diversity among patients with Lemierre syndrome and clinical implications: an individual patient-level analysis.

Journal: Infection

Published: December 08, 2024

Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis.

Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis.

Journal: British journal of haematology

Published: July 23, 2024

Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.

Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.

Journal: British journal of haematology

Published: January 19, 2024

ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype.

ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype.

Journal: British journal of haematology

Published: November 13, 2023

Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation.

Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet Differentiation.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: October 31, 2023

Common laboratory tests and their correlation with the clinical presentation and prognosis of Lemierre syndrome.

Common laboratory tests and their correlation with the clinical presentation and prognosis of Lemierre syndrome.

Journal: Anaerobe

Published: May 04, 2023

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

Showing 1-12 of 99

Last Updated: 09/26/2026