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Platelets as Mediators of Thromboinflammation in Chronic Myeloproliferative Neoplasms

Frontiers in immunology, 2019-06, Vol.10, p.1373-1373

2019

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Platelet Apoptosis in Adult Immune Thrombocytopenia: Insights into the Mechanism of Damage Triggered by Auto-Antibodies

PloS one, 2016-08, Vol.11 (8), p.e0160563-e0160563

2016

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Platelet Toll-Like Receptors Mediate Thromboinflammatory Responses in Patients With Essential Thrombocythemia

Frontiers in immunology, 2020-04, Vol.11, p.705-705

2020

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Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia

Haematologica (Roma), 2019-06, Vol.104 (6), p.1244-1255

2019

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Megakaryocyte–stromal cell interactions: Effect on megakaryocyte proliferation, proplatelet production, and survival

Experimental hematology, 2022-03, Vol.107, p.24-37

2022

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First description of revertant mosaicism in familial platelet disorder with predisposition to acute myelogenous leukemia: correlation with the clinical phenotype

Haematologica (Roma), 2020-10, Vol.105 (10), p.e535

2020

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RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

Seminars in hematology, 2017-04, Vol.54 (2), p.75-80

2017

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High cell-free DNA is associated with disease progression, inflammasome activation and elevated levels of inflammasome-related cytokine IL-18 in patients with myelofibrosis

Frontiers in immunology, 2023-11, Vol.14, p.1161832-1161832

2023

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Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus

Platelets (Edinburgh), 2022-07, Vol.33 (5), p.743-754

2022

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency

Haematologica (Roma), 2013-06, Vol.98 (6), p.868-874

2013

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Abnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patients

Scientific reports, 2016-03, Vol.6 (1), p.23213-23213, Article 23213

2016

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Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel

Blood advances, 2021-01, Vol.5 (2), p.414-431

2021

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Differential expression of SDF-1 receptor CXCR4 in molecularly defined forms of inherited thrombocytopenias

Platelets (Edinburgh), 2017-08, Vol.28 (6), p.602-606

2017

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Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Blood, 2014-08, Vol.124 (6), p.e4-e10

2014

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

British journal of haematology, 2024-10

2024

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Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression

Blood, 2012-09, Vol.120 (13), p.2708-2718

2012

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MYH9 -related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations

European journal of medical genetics, 2013-01, Vol.56 (1), p.7-12

2013

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

Journal of thrombosis and haemostasis, 2021-05, Vol.19 (5), p.1364-1371

2021

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Neutrophil extracellular trap formation and circulating nucleosomes in patients with chronic myeloproliferative neoplasms

Scientific reports, 2016-12, Vol.6 (1), p.38738-38738, Article 38738

2016

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MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

Human mutation, 2014-02, Vol.35 (2), p.236-247

2014

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Toll-like receptor expression and functional behavior in platelets from patients with systemic lupus erythematosus

Immunobiology (1979), 2024-01, Vol.229 (1), p.152782-152782, Article 152782

2024

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Platelets as Mediators of Thromboinflammation in Chronic Myeloproliferative Neoplasms

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

ANKRD26-related thrombocytopenia and myeloid malignancies

Platelet Apoptosis in Adult Immune Thrombocytopenia: Insights into the Mechanism of Damage Triggered by Auto-Antibodies

Platelet Toll-Like Receptors Mediate Thromboinflammatory Responses in Patients With Essential Thrombocythemia

Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia

Megakaryocyte–stromal cell interactions: Effect on megakaryocyte proliferation, proplatelet production, and survival

First description of revertant mosaicism in familial platelet disorder with predisposition to acute myelogenous leukemia: correlation with the clinical phenotype

RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM)

Elevated levels of damage-associated molecular patterns HMGB1 and S100A8/A9 coupled with toll-like receptor-triggered monocyte activation are associated with inflammation in patients with myelofibrosis

High cell-free DNA is associated with disease progression, inflammasome activation and elevated levels of inflammasome-related cytokine IL-18 in patients with myelofibrosis

Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study

Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus

Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency

Abnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patients

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel

Differential expression of SDF-1 receptor CXCR4 in molecularly defined forms of inherited thrombocytopenias

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

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

Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression

MYH9 -related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations

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

Neutrophil extracellular trap formation and circulating nucleosomes in patients with chronic myeloproliferative neoplasms

MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations

Toll-like receptor expression and functional behavior in platelets from patients with systemic lupus erythematosus

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