Veronica Palma-Barqueros
Overview
Explore the profile of Veronica Palma-Barqueros including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
190
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Recent Articles
1.
Palma-Barqueros V, Bastida J, Lopez Andreo M, Zamora-Canovas A, Zaninetti C, Ruiz-Pividal J, et al.
J Thromb Haemost
. 2023 Feb;
21(5):1352-1365.
PMID: 36736831
Background: Germline mutations in RUNX1 can cause a familial platelet disorder that may lead to acute myeloid leukemia, an autosomal dominant disorder characterized by moderate thrombocytopenia, platelet dysfunction, and a...
2.
Bastida J, Malvestiti S, Boeckelmann D, Palma-Barqueros V, Wolter M, Lozano M, et al.
Cells
. 2022 Oct;
11(20).
PMID: 36291092
The GATA1 transcription factor is essential for normal erythropoiesis and megakaryocytic differentiation. Germline GATA1 pathogenic variants in the N-terminal zinc finger (N-ZF) are typically associated with X-linked thrombocytopenia, platelet dysfunction,...
3.
Palma-Barqueros V, Revilla N, Zaninetti C, Galera A, Sanchez-Fuentes A, Zamora-Canovas A, et al.
Blood Adv
. 2022 Mar;
6(17):5244-5255.
PMID: 35349645
Src-related thrombocytopenia (SRC-RT) is a rare autosomal dominant, inherited platelet disorder resulting from the p.E527K heterozygous germline gain-of-function variant of Src. To date, genetic diagnosis of the disease has only...
4.
Marin-Quilez A, Vuelta E, Diaz-Ajenjo L, Fernandez-Infante C, Garcia-Tunon I, Benito R, et al.
J Thromb Haemost
. 2022 Feb;
20(5):1248-1255.
PMID: 35170221
Background: Rare inherited thrombocytopenias are caused by alterations in genes involved in megakaryopoiesis, thrombopoiesis and/or platelet release. Diagnosis is challenging due to poor specificity of platelet laboratory assays, large numbers...
5.
Palma-Barqueros V, Bury L, Kunishima S, Lozano M, Rodriguez-Alen A, Revilla N, et al.
Blood Adv
. 2021 Sep;
5(24):5453-5467.
PMID: 34516618
β1-Tubulin plays a major role in proplatelet formation and platelet shape maintenance, and pathogenic variants in TUBB1 lead to thrombocytopenia and platelet anisocytosis (TUBB1-RT). To date, the reported number of...
6.
Palma-Barqueros V, Revilla N, Sanchez A, Zamora Canovas A, Rodriguez-Alen A, Marin-Quilez A, et al.
Int J Mol Sci
. 2021 Apr;
22(9).
PMID: 33926054
Platelets play a major role in hemostasis as ppwell as in many other physiological and pathological processes. Accordingly, production of about 10 platelet per day as well as appropriate survival...
7.
Marin-Quilez A, Garcia-Tunon I, Fernandez-Infante C, Hernandez-Cano L, Palma-Barqueros V, Vuelta E, et al.
Thromb Haemost
. 2021 Feb;
121(9):1193-1205.
PMID: 33626581
-related disorder (-RD) is caused by germline variants affecting the gene. This rare, heterogeneous disorder has no specific clinical or laboratory phenotype, making genetic diagnosis necessary. Although international recommendations have...
8.
Palma-Barqueros V, Crescente M, de la Morena M, Chan M, Almarza E, Revilla N, et al.
Am J Hematol
. 2020 Dec;
96(3):E83-E88.
PMID: 33326144
No abstract available.
9.
Palma-Barqueros V, Bohdan N, Revilla N, Vicente V, Bastida J, Rivera J
Platelets
. 2020 Jun;
32(5):710-716.
PMID: 32584621
No abstract available.
10.
Lee R, Piatt R, Dhenge A, Lozano M, Palma-Barqueros V, Rivera J, et al.
Sci Transl Med
. 2019 Dec;
11(522).
PMID: 31826978
Platelet transfusions can fail to prevent bleeding in patients with inherited platelet function disorders (IPDs), such as Glanzmann's thrombasthenia (GT; integrin αIIbβ3 dysfunction), Bernard-Soulier syndrome [BSS; glycoprotein (GP) Ib/V/IX dysfunction],...