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Verónica Palma-Barqueros

University of Murcia

19

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166

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Inherited Platelet Disorders: An Updated Overview.

2021 International Journal of Molecular Sciences
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Identification By Whole Exome Sequencing of the Molecular Defect in a Novel Gene Related to Glycosylation in Two Unrelated Families with Syndromic Macrothrombocytopenia

2021 Blood
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PTGS1 gene variations associated with bleeding and platelet dysfunction.

2020 Platelets
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RASGRP2 gene variations associated with platelet dysfunction and bleeding

2019 Platelets
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Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing

2019 Annals of Medicine
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Strategies for Analysis of Novel Molecular Variants in the RUNX1 Gene As a Cause of Familial Platelet Disorder with Predisposition to Acute Myeloid Leukemia (FPD/AML)

2019 Blood
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Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders

2019 Seminars in Thrombosis and Hemostasis
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Developmental Differences in Platelet Inhibition Response to Prostaglandin E1.

2019 Neonatology
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Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders

2018 Haematologica
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Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications

2018 Blood
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