J. Rivera

发表

Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders

J. Hernández-Rivas, J. González-Porras, R. Benito, 2019, Seminars in Thrombosis and Hemostasis.

A Modern Approach to the Molecular Diagnosis of Inherited Bleeding Disorders

V. Vicente, R. Benito, J. M. Bastida, 2018 .

The association of the beta1-tubulin Q43P polymorphism with intracerebral hemorrhage in men.

J. Montaner, J. Corral, V. Vicente, 2007, Haematologica.

Compliance with temperature and time requirements during in-hospital distribution of blood components: A national survey among transfusion services.

A. Castrillo, I. Romon, J. Rivera, 2020, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Evaluation of platelet function during extended storage in additive solution, prepared in a new container that allows manual buffy-coat platelet pooling and leucoreduction in the same system.

V. Vicente, J. Egea, M. Lozano, 2012, Blood transfusion = Trasfusione del sangue.

The influence of riboflavin photochemistry on plasma coagulation factors.

V. Vicente, J. Rivera, L. Larrea, 2009, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Effect of rhG-CSF on the mobilization of CD38 and HLA-DR subfractions of CD34+ peripheral blood progenitor cells

F. Ortuño, J. Rivera, M. Lozano, 1995, Annals of Hematology.

Cryopreservation Modifies Flow‐Cytometric Analysis of Hemopoietic Cells

F. Ortuño, J. Rivera, V. Vicente, 1995, Vox sanguinis.

Effect of quercetin on platelet spreading on collagen and fibrinogen and on multiple platelet kinases.

V. Vicente, L. Navarro-Núñez, C. Martínez, 2010, Fitoterapia.

Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease.

J. Corral, V. Vicente, M. Lozano, 1998, Blood.

Genetic polymorphisms of factor VII are not associated with arterial thrombosis

J. Corral, V. Vicente, M. Lozano, 1998, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Temporal Changes in Platelet Response in Acute Coronary Syndrome Patients With Prasugrel and Clopidogrel After Stent Implantation.

M. Valdés, E. Orenes-Piñero, A. Tello-Montoliu, 2017, Circulation journal : official journal of the Japanese Circulation Society.

Inherited Platelet Disorders: An Updated Overview

J. González-Porras, V. Vicente, J. M. Bastida, 2021, International journal of molecular sciences.

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

J. Hernández-Rivas, I. García-Tuñón, J. González-Porras, 2022, Journal of thrombosis and haemostasis : JTH.

Platelet GP Ib/IX/V complex: physiological role

J. Corral, V. Vicente, C. Martínez, 2000, Journal of Physiology and Biochemistry.

Role of the 807 C/T Polymorphism of the α2 Gene in Platelet GP Ia Collagen Receptor Expression and Function

F. Ortuño, J. Corral, V. Vicente, 1999, Thrombosis and Haemostasis.

Clinical and analytical relevance of the combination of prothrombin 20210A/A and factor V Leiden: results from a large family

J. Corral, V. Vicente, J. Rivera, 1999, British journal of haematology.

The prothrombin gene variant 20210A in venous and arterial thromboembolism.

J. Corral, V. Vicente, J. Rivera, 1999, Haematologica.

HPA-1 genotype in arterial thrombosis--role of HPA-1b polymorphism in platelet function.

J. Corral, V. Vicente, M. Lozano, 1997, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Platelet aggregation through prothrombinase activation induced by non-aggregant doses of platelet agonists

J. Corral, V. Vicente, C. Martínez, 2002, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

A common polymorphism in the annexin V Kozak sequence (-1C>T) increases translation efficiency and plasma levels of annexin V, and decreases the risk of myocardial infarction in young patients.

F. Marín, J. Corral, V. Vicente, 2002, Blood.

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

S. Mundell, M. Simpson, S. Watson, 2016, Haematologica.

A Common Polymorphism Flanking the ATG Initiator Codon of GPIbα Does not Affect Expression and Is not a Major Risk Factor for Arterial Thrombosis

J. Corral, V. Vicente, C. Martínez, 2000, Thrombosis and Haemostasis.

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

W. Bergmeier, Ankita Dhenge, M. Lozano, 2019, Science Translational Medicine.

Influence of CYP2C19 polymorphisms in platelet reactivity and prognosis in an unselected population of non ST elevation acute coronary syndrome.

M. Valdés, A. Tello-Montoliu, F. Marín, 2012, Revista espanola de cardiologia.

Influence of CYP2C19 Polymorphisms in Platelet Reactivity and Prognosis in an Unselected Population of Non ST Elevation Acute Coronary Syndrome

M. Valdés, A. Tello-Montoliu, F. Marín, 2012 .

Platelet reactivity over time in coronary artery disease patients treated with a bioabsorbable everolimus-eluting scaffold

M. Valdés, J. Ferreiro, E. Orenes-Piñero, 2016, Platelets.

Consensus recommendations on flow cytometry for the assessment of inherited and acquired disorders of platelet number and function: Communication from the ISTH SSC Subcommittee on Platelet Physiology

A. Michelson, A. L. Frelinger, M. Lordkipanidzé, 2021, Journal of thrombosis and haemostasis : JTH.

Role of factor XIII Val34Leu polymorphism in patients <45 years of age with acute myocardial infarction.

F. Marín, J. Corral, V. Vicente, 2003, The American journal of cardiology.

Antioxidant and Anti-Inflammatory Strategies Based on the Potentiation of Glutathione Peroxidase Activity Prevent Endothelial Dysfunction in Chronic Kidney Disease

M. Díaz-Ricart, G. Escolar, J. Cruzado, 2018, Cellular Physiology and Biochemistry.

Effect of cold-storage in the accumulation of bioreactive substances in platelet concentrates treated with second messenger effects.

J. Corral, M. Lozano, J. Rivera, 2001, Haematologica.

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

J. Hernández-Rivas, T. Warner, J. González-Porras, 2020, American journal of hematology.

PTGS1 gene variations associated with bleeding and platelet dysfunction

V. Vicente, J. M. Bastida, J. Rivera, 2020, Platelets.

Biological Assessment of Aspirin Efficacy on Healthy Individuals: Heterogeneous Response or Aspirin Failure?

J. Corral, J. Guerrero, J. Rivera, 2005, Stroke.

Thromboxane A2 receptor antagonism by flavonoids: structure-activity relationships.

V. Vicente, L. Navarro-Núñez, C. Martínez, 2009, Journal of agricultural and food chemistry.

Running title : β-tubulin VI variability and paclitaxel toxicity 1 Title : Hematologi β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity

L. Inglada-Perez, R. Letón, C. Rodríguez-Antona, 2012 .

Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity.

L. Inglada-Perez, R. Letón, C. Rodríguez-Antona, 2012, Cancer research.

Apigenin inhibits platelet adhesion and thrombus formation and synergizes with aspirin in the suppression of the arachidonic acid pathway.

M. Díaz-Ricart, G. Escolar, V. Vicente, 2008, Journal of agricultural and food chemistry.

Flavonoids inhibit the platelet TxA(2) signalling pathway and antagonize TxA(2) receptors (TP) in platelets and smooth muscle cells.

V. Vicente, L. Navarro-Núñez, J. Guerrero, 2007, British journal of clinical pharmacology.

The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease

J. Corral, V. Vicente, M. Lozano, 1997, British journal of haematology.

Differential effects of quercetin, apigenin and genistein on signalling pathways of protease‐activated receptors PAR1 and PAR4 in platelets

V. Vicente, L. Navarro-Núñez, J. Guerrero, 2009, British journal of pharmacology.

ISTH Advanced Training Course on platelet bleeding disorders: How should they be investigated?

S. Watson, Andrew Paterson, N. Morgan, 2016, Platelets.

Down Regulation of the Munc18b-syntaxin-11 Complex and β1-tubulin Impairs Secretion and Spreading in Neonatal Platelets

V. Vicente, J. Delgado, R. Teruel-Montoya, 2017, Thrombosis and Haemostasis.

The FXIII Val34Leu polymorphism in venous and arterial thromboembolism.

J. Corral, V. Vicente, C. Martínez, 2000, Haematologica.

Loss of high‐affinity thrombin receptors during platelet concentrate storage impairs the reactivity of platelets to thrombin

V. Vicente, M. Lozano, J. Rivera, 1997, Transfusion.

Latent and Polymeric Antithrombin: Clearance and Potential Thrombotic Risk

J. Corral, V. Vicente, L. Navarro-Núñez, 2007, Experimental biology and medicine.

Impaired leucocyte activation is underlining the lower thrombotic risk of essential thrombocythaemia patients with CALR mutations as compared with those with the JAK2 mutation

V. Vicente, C. Martínez, F. Ferrer-Marín, 2016, British journal of haematology.

Factor XIII Val34Leu polymorphism in primary intracerebral haemorrhage.

J. Corral, V. Vicente, J. Rivera, 2000, The hematology journal : the official journal of the European Haematology Association.

Evaluation of refrigerated platelet concentrates supplemented with low doses of second messenger effectors.

J. Corral, V. Vicente, J. Guerrero, 2004, Clinical and laboratory haematology.

[Bernard -Soulier syndrome].

J. Rivera, J. Moraleda, M. Sánchez, 1992, Sangre.

Proteomic analysis of platelet N-glycoproteins in PMM2-CDG patients.

M. Di Michele, J. Corral, V. Vicente, 2014, Thrombosis research.

L718P mutation in the membrane-proximal cytoplasmic tail of β3 promotes abnormal αIIbβ3 clustering and lipid microdomain coalescence, and associates with a thrombasthenia-like phenotype

P. Lastres, V. Vicente, C. Martínez, 2010, Haematologica.

Expanding the genetic spectrum of TUBB1-related thrombocytopenia

V. Vicente, P. Gresele, L. Bury, 2021, Blood advances.

JAK2 V617F, hemostatic polymorphisms, and clinical features as risk factors for arterial thrombotic events in essential thrombocythemia

B. Bellosillo, V. Vicente, L. Navarro-Núñez, 2008, Annals of Hematology.

Binding of Recombinant Apolipoprotein(a) to Human Platelets and Effect on Platelet Aggregation

J. Corral, V. Vicente, E. Angles-cano, 2001, Thrombosis and Haemostasis.

Migraine and Prothrombotic Genetic Risk Factors

J. Corral, V. Vicente, M. Lozano, 1998, Cephalalgia : an international journal of headache.

DDAVP and Tachyphylaxis in Healthy Subjects

A. Estellés, J. Aznar, J. Rivera, 1993 .

In vitro analysis of platelet concentrates stored in the presence of modulators of 3',5' adenosine monophosphate, and organic anions.

J. Corral, V. Vicente, E. Bermejo, 2000, Transfusion science.

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

W. Ouwehand, K. Downes, D. Trégouët, 2021, Journal of thrombosis and haemostasis : JTH.

Tubulin in Platelets: When the Shape Matters

R. Teruel-Montoya, F. Ferrer-Marín, J. Rivera, 2019, International journal of molecular sciences.

Significant Hypo-Responsiveness to GPVI and CLEC-2 Agonists in Pre-Term and Full-Term Neonatal Platelets and following Immune Thrombocytopenia

S. Watson, V. Vicente, J. Delgado, 2018, Thrombosis and Haemostasis.

Absence of Effect of DDAVP Infusion on Platelet Glycoprotein Ib/IX and IIb/IIIa Complexes, and their Interaction with Newly Released von Willebrand Factor.

A. Pereira, M. Roig, J. Rivera, 1993, Platelets.

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3

J. Corral, V. Vicente, C. Martínez, 2015, Journal of clinical neurology.

A radioreceptor assay for mass measurement of inositol (1,4,5)-trisphosphate using saponin-permeabilized outdated human platelets.

J. Corral, V. Vicente, F. de Arriba, 1998, Analytical biochemistry.

Genotype–phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause

J. Corral, V. Vicente, L. Navarro-Núñez, 2009, British journal of haematology.

Two novel variants of the ABCG5 gene cause xanthelasmas and macrothrombocytopenia: a brief review of hematologic abnormalities of sitosterolemia

J. Hernández-Rivas, J. González-Porras, R. Benito, 2017, Journal of thrombosis and haemostasis : JTH.

Detection of conformational transformation of antithrombin in blood with crossed immunoelectrophoresis: new application for a classical method.

J. Corral, V. Vicente, A. Miñano, 2003, The Journal of laboratory and clinical medicine.

Evaluation of a new whole‐blood filter that allows preparation of platelet concentrates by platelet‐rich plasma methods

V. Vicente, M. Lozano, J. Rivera, 2003, Transfusion.

Evaluation of pooled platelet concentrates using prestorage versus poststorage WBC reduction: impact of filtration timing

J. Corral, M. Lozano, J. Rivera, 2000, Transfusion.

ABCG5 and ABCG8 gene variations associated with sitosterolemia and platelet dysfunction

J. González-Porras, R. Benito, J. M. Bastida, 2020, Platelets.

Stability of Glycoproteins Ib/IX and IIb/IIIa during Preparation and Storage of Platelet Concentrates: Detection by Binding Assays with Epitope‐Defined Monoclonal Antibodies and Physiological Ligands

J. Rivera, J. Moraleda, M. C. Rosillo, 1994, Vox sanguinis.

Repeated infusions of DDAVP induce low response of FVIII and vWF but not of plasminogen activators.

A. Estellés, J. Aznar, J. Rivera, 1993, Thrombosis research.

Prothrombotic Genetic Risk Factors in Patients With Coexisting Migraine and Ischemic Cerebrovascular Disease

J. Corral, V. Vicente, J. Rivera, 1999, Headache.

Towards the targeted management of Chediak-Higashi syndrome

V. Vicente, M. Lozano, J. Rivera, 2014, Orphanet Journal of Rare Diseases.

Hermansky-Pudlak syndrome

V. Vicente, M. Lozano, J. Rivera, 2014, Hämostaseologie.

Platelet cryopreservation using a reduced dimethyl sulfoxide concentration and second-messenger effectors as cryopreserving solution.

J. Corral, V. Vicente, M. Lozano, 1999, Cryobiology.

In Vitro Changes of Platelet Parameters

V. Vicente, M. Lozano, J. Rivera, 2004 .

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

P. Nurden, P. Noris, R. Favier, 2019, Haematologica.

von Willebrand factor contained in a high purity FVIII concentrate (Fanhdi) binds to platelet glycoproteins and supports platelet adhesion to subendothelium under flow conditions.

G. Escolar, M. Bravo, J. Jorquera, 1999, Haematologica.

Evaluation of four rapid methods for hemoglobin screening of whole blood donors in mobile collection settings.

J. Corral, V. Vicente, L. Navarro-Núñez, 2007, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Flavonoids inhibit platelet function through binding to the thromboxane A2 receptor

V. Vicente, J. Guerrero, M. Lozano, 2005, Journal of thrombosis and haemostasis : JTH.

Platelet receptors and signaling in the dynamics of thrombus formation

V. Vicente, L. Navarro-Núñez, M. Lozano, 2009, Haematologica.

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

J. Hernández-Rivas, Jorge Oliveira, J. González-Porras, 2019, Annals of medicine.

Hsp70 protects from stroke in atrial fibrillation patients by preventing thrombosis without increased bleeding risk.

O. Rabal, J. Oyarzábal, J. González-Porras, 2016, Cardiovascular research.

University of Birmingham Novel mutations in RASGRP2 encoding for CalDAG-GEFI abrogate Rap1 activation causing platelet dysfunction

David S. Paul, S. Watson, J. Sondek, 2016 .

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study

V. Vicente, A. Cid, M. Lozano, 2014, Orphanet Journal of Rare Diseases.

Genetic variants of the extra‐large stimulatory Gs protein alpha‐subunit and risk of thrombotic and haemorrhagic disorders

J. Corral, V. Vicente, J. Guerrero, 2004, British journal of haematology.

Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene.

P. Real, V. Vicente, V. Ramos-Mejia, 2016, Stem cell research.

Role of Thrombopoietin Receptor Agonists in Inherited Thrombocytopenia

J. González-Porras, J. M. Bastida, M. Lozano, 2021, International journal of molecular sciences.

Phenotype description and response to thrombopoietin receptor agonist in DIAPH1-related disorder.

Wendy N Erber, Chantal Thys, Kate Downes, 2018, Blood advances.

Wiskott–Aldrich syndrome in a child presenting with macrothrombocytopenia

M. Pérez‐Andrés, Elena Blanco, V. Vicente, 2017, Platelets.

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

M. Simpson, S. Watson, M. Lordkipanidzé, 2015, The Journal of clinical investigation.

An atypical IgM class platelet cold agglutinin induces GPVI-dependent aggregation of human platelets

S. Watson, V. Vicente, I. Martínez-Martínez, 2015, Thrombosis and Haemostasis.

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

N. Morgan, K. Freson, R. Benito, 2022, Cells.

A. Greinacher, V. Vicente, C. Zaninetti, 2022, Blood advances.

Allogeneic hematopoietic cell transplantation in an adult patient with Glanzmann thrombasthenia

M. Sanz, V. Vicente, J. Sanz, 2017, Clinical case reports.

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

J. Hernández-Rivas, S. Watson, J. González-Porras, 2017, Haematologica.

Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunction.

David S. Paul, J. Hernández-Rivas, S. Watson, 2016, Blood.

Chediak–Higashi syndrome: description of two novel homozygous missense mutations causing divergent clinical phenotype

F. Ortuño, V. Vicente, N. García-Barberá, 2014, European journal of haematology.

Quality assessment and transfusion efficacy of buffy coat-derived platelet concentrates washed with platelet additive solution.

V. Vicente, F. Ferrer-Marín, M. Lozano, 2018, Blood transfusion = Trasfusione del sangue.

The PI3Kδ Inhibitor Idelalisib Diminishes Platelet Function and Shows Antithrombotic Potential

M. Loza, Ángel García, E. Domínguez, 2021, International journal of molecular sciences.

Frozen and cold-stored platelets: reconsidered platelet products

V. Vicente, A. Castrillo, J. Rivera, 2021, Platelets.

Association of autoantibodies against platelet glycoproteins Ib/IX and IIb/IIIa, and platelet‐reactive anti‐HIV antibodies in thrombocytopenic narcotic addicts

V. Vicente, J. Rivera, A. Cano, 1996, British journal of haematology.

Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with Thrombocytopenia

D. Kelsell, M. Simpson, M. Akiyama, 2017, Journal of Investigative Dermatology.

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

J. Hernández-Rivas, M. Sánchez-Martín, I. García-Tuñón, 2021, Thrombosis and Haemostasis.

The number of platelet glycoprotein Ia molecules is associated with the genetically linked 807 C/T and HPA‐5 polymorphisms

J. Corral, V. Vicente, J. Rivera, 1999, Transfusion.

High on-treatment platelet reactivity in patients with ischemic cerebrovascular disease: assessment of prevalence and stability over time using four platelet function tests

V. Vicente, C. Martínez, E. Jover, 2014, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Quality assessment of buffy‐coat‐derived leucodepleted platelet concentrates in PAS‐plasma, prepared by the OrbiSac or TACSI automated system

J. Rivera, E. M. Plaza, J. Egea, 2014, Vox sanguinis.

Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children

J. Corral, V. Vicente, J. Soria, 2011, Haematologica.

Comparative assessment of prophylactic transfusions of platelet concentrates obtained by the PRP or buffy-coat methods, in patients undergoing allogeneic hematopoietic stem cell transplantation

J. Rivera‐Caravaca, V. Vicente, F. de Arriba, 2018, Hematology.

Comprehensive comparison of neonate and adult human platelet transcriptomes

V. Vicente, R. Teruel-Montoya, C. Martínez, 2017, PloS one.

RASGRP2 gene variations associated with platelet dysfunction and bleeding

V. Vicente, J. M. Bastida, M. Lozano, 2019, Platelets.

Identification of two novel mutations in RASGRP2 affecting platelet CalDAG-GEFI expression and function in patients with bleeding diathesis

David S. Paul, J. Hernández-Rivas, S. Watson, 2017, Platelets.

Effect of Factor XIII VAL34LEU Polymorphism on Thrombolytic Therapy in Premature Myocardial Infarction

F. Marín, J. Corral, V. Vicente, 2002, Thrombosis and Haemostasis.

Successful mobilization of hematopoietic peripheral blood progenitor cells with paclitaxel-based chemotherapy as initial or salvage regimen in patients with hematologic malignancies

V. Vicente, F. de Arriba, M. Lozano, 2008, Haematologica.

Comparative study of three methods to detect free plasma antiplatelet antibodies.

M. Lozano, J. Rivera, R. González-Conejero, 1996, Acta haematologica.

TUBB1 Q43P polymorphism does not protect against acute coronary syndrome and premature myocardial infarction

F. Marín, V. Vicente, C. Martínez, 2008, Thrombosis and Haemostasis.

Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation

A. Balduini, J. González-Porras, R. Benito, 2023, International journal of molecular sciences.

GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant.

P. Real, I. Simon, J. Marchal, 2019, Stem cell research.

Effect of G-CSF on the Haemostatic System

J. Rivera, I. Zuazu, V. Vicente, 1994, Thrombosis and Haemostasis.

New perspectives in antiplatelet therapy.

D. Angiolillo, A. Tello-Montoliu, F. Marín, 2012, Current medicinal chemistry.

Evaluation of two‐step haemoglobin screening with HemoCue for blood donor qualification in mobile collection sites

F. Ferrer-Marín, M. Lozano, J. Rivera, 2014, Vox sanguinis.

Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure

P. Nurden, J. Corral, V. Vicente, 2011, Thrombosis and Haemostasis.

Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: Identification of the second HPS7 mutation in a patient presenting late in life

S. Watson, M. Lordkipanidzé, N. Morgan, 2013, Thrombosis and Haemostasis.

New alleles of the platelet glycoprotein Ibalpha gene.

J. Corral, V. Vicente, M. Lozano, 1998, British Journal of Haematology.

Developmental Differences in Platelet Inhibition Response to Prostaglandin E1

V. Vicente, R. Teruel-Montoya, A. Begonja, 2019, Neonatology.

Molecular, ultrastructural and functional characterization of a Spanish family with Hermansky–Pudlak syndrome: role of insC974 in platelet function and clinical relevance

G. Escolar, J. Corral, V. Vicente, 2003, British journal of haematology.

Induced pluripotent stem cells derived from Bernard-Soulier Syndrome patient's peripheral blood cells with a p.Phe55Ser mutation in the GPIX gene.

P. Real, V. Vicente, V. Ramos-Mejia, 2017, Stem Cell Research.

Generation of a human induced pluripotent stem cell (iPSC) line from a Bernard-Soulier syndrome patient with the mutation p.Asn45Ser in the GPIX gene.

P. Real, V. Vicente, V. Ramos-Mejia, 2016, Stem cell research.

Evaluation of Leukocyte‐Depleted Platelet Concentrates Obtained by In‐Line Filtration

J. Corral, V. Vicente, J. Rivera, 2000, Vox Sanguinis.

In vitro changes of platelet parameters: lessons from blood banking.

V. Vicente, M. Lozano, J. Rivera, 2004, Methods in molecular biology.

Inherited Platelet Disorders: An Updated Overview

J. González-Porras, V. Vicente, M. Lozano, 2021, International Journal of Molecular Sciences.

GALE variants associated with syndromic manifestations, macrothrombocytopenia, bleeding, and platelet dysfunction.

A. Balduini, R. Benito, C. D. Di Buduo, 2023, Platelets.

Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with Thrombocytopenia

D. Kelsell, M. Simpson, M. Akiyama, 2017, The Journal of investigative dermatology.

Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C

P. Real, U. Modlich, V. Ramos-Mejia, 2023, Molecular therapy. Nucleic acids.

Genotype–phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause

J. Corral, V. Vicente, O. Panes, 2009, British journal of haematology.