Veronica Barqueros-Palma

Murcia, MU, Spain

Last Updated: 09/26/2026

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Found 18 publications

Platelet transcriptome analysis in patients with germline RUNX1 mutations.

Platelet transcriptome analysis in patients with germline RUNX1 mutations.

Journal: Journal of thrombosis and haemostasis : JTH

Published: August 22, 2022

A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.

A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.

Journal: Cells

Published: July 27, 2022

A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling.

A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling.

Journal: Journal of thrombosis and haemostasis : JTH

Published: November 21, 2021

Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease.

Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease.

Journal: Blood advances

Published: June 02, 2021

Inherited Platelet Disorders: An Updated Overview.

Inherited Platelet Disorders: An Updated Overview.

Journal: International journal of molecular sciences

Published: March 31, 2021

Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model.

Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model.

Journal: Thrombosis and haemostasis

Published: February 24, 2021

Expanding the genetic spectrum of TUBB1-related thrombocytopenia.

Expanding the genetic spectrum of TUBB1-related thrombocytopenia.

Journal: Blood advances

Published: December 16, 2020

A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis.

A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis.

Journal: American journal of hematology

Published: October 22, 2020

PTGS1 gene variations associated with bleeding and platelet dysfunction.

PTGS1 gene variations associated with bleeding and platelet dysfunction.

Journal: Platelets

Published: June 26, 2020

Developmental Differences in Platelet Inhibition Response to Prostaglandin E1.

Developmental Differences in Platelet Inhibition Response to Prostaglandin E1.

Journal: Neonatology

Published: July 22, 2019

Impaired hemostatic activity of healthy transfused platelets in inherited and acquired platelet disorders: Mechanisms and implications.

Impaired hemostatic activity of healthy transfused platelets in inherited and acquired platelet disorders: Mechanisms and implications.

Journal: Science translational medicine

Published: May 13, 2019

Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders.

Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders.

Journal: Seminars in thrombosis and hemostasis

Published: May 02, 2019

Showing 1-12 of 18

Last Updated: 09/26/2026