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Sensitivity to Deviance and to Dissimilarity: Basic Cognitive Processes Under Activation of the Behavioral Immune System

Evolutionary psychology, 2018-10, Vol.16 (4), p.1474704918813433-1474704918813433

2018

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The Organophosphate Paraoxon and Its Antidote Obidoxime Inhibit Thrombin Activity and Affect Coagulation In Vitro

PloS one, 2016-09, Vol.11 (9), p.e0163787-e0163787

2016

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Novel mutation in coagulation factor VII (Carmel mutation): Identification and characterization

Research and practice in thrombosis and haemostasis, 2021-05, Vol.5 (4), p.e12407-n/a, Article e12407

2021

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A Novel Compound Targeting Protease Receptor 1 Activators for the Treatment of Glioblastoma

Frontiers in neurology, 2018-12, Vol.9, p.1087-1087

2018

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Antiplatelet Effect of Thienopyridine ( Clopidogrel or Prasugrel ) Pretreatment in Patients Undergoing Primary Percutaneous Intervention for ST Elevation Myocardial Infarction

The American journal of cardiology, 2013-11, Vol.112 (10), p.1551-1556

2013

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Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Thrombosis and haemostasis, 2007-12, Vol.98 (12), p.1257-1265

2007

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Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.36923-36930

2001

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Predicting risk severity and response of fetal neonatal alloimmune thrombocytopenia

British journal of haematology, 2013-08, Vol.162 (3), p.304-312

2013

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Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Blood, 2002-04, Vol.99 (7), p.2448-2454

2002

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Blood, 1998-08, Vol.92 (4), p.1119-1124

1998

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Molecular insight into human platelet antigens: structural and evolutionary conservation analyses offer new perspective to immunogenic disorders

Transfusion (Philadelphia, Pa.), 2011-03, Vol.51 (3), p.558-569

2011

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Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomerase

Experimental cell research, 2019-08, Vol.381 (1), p.77-85

2019

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Prospective Controlled Monitoring of Hemlibra Prophylaxis Initiation in a Large Cohort of Hemophilia a Patients- Real World Data

Blood, 2019-11, Vol.134 (Supplement_1), p.2397-2397

2019

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Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients

Thrombosis and haemostasis, 2019-01, Vol.119 (1), p.117-127

2019

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Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomerase

Experimental cell research, 2019-08, Vol.381 (1), p.77-85

2019

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Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients

Blood cells, molecules, & diseases, 2021-07, Vol.89, p.102560-102560, Article 102560

2021

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Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Blood, 2015-07, Vol.126 (5), p.661-664

2015

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Platelets from Calreticulin mutated essential thrombocythemia patients are less reactive than JAK2 V617F mutated platelets

American journal of hematology, 2020-04, Vol.95 (4), p.379-386

2020

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Unique Disulfide Bonds in Epidermal Growth Factor (EGF) Domains of β3 Affect Structure and Function of αIIbβ3 and αvβ3 Integrins in Different Manner

The Journal of biological chemistry, 2012-03, Vol.287 (12), p.8879-8891

2012

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Application of a clinical decision rule and laboratory assays in pediatrics: Adult heparin‐induced thrombocytopenia

Pediatric blood & cancer, 2022-11, Vol.69 (11), p.e29929-n/a

2022

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Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombasthenia

Haematologica (Roma), 2007-05, Vol.92 (5), p.698-701

2007

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A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients

Hepatology research, 2005-02, Vol.31 (2), p.104-111

2005

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Pediatric immune thrombocytopenia: apoptotic markers may help in predicting the disease course

Pediatric research, 2021-07, Vol.90 (1), p.93-98

2021

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A Simple Two Step Approach for Diagnosis of Heparin Induced Thrmbocytopenia Using 4T Score and PaGIA Testing

Blood, 2014-12, Vol.124 (21), p.1449-1449

2014

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Spectrum of the Mutations in Bernard-Soulier Syndrome

Sensitivity to Deviance and to Dissimilarity: Basic Cognitive Processes Under Activation of the Behavioral Immune System

The Organophosphate Paraoxon and Its Antidote Obidoxime Inhibit Thrombin Activity and Affect Coagulation In Vitro

Novel mutation in coagulation factor VII (Carmel mutation): Identification and characterization

A Novel Compound Targeting Protease Receptor 1 Activators for the Treatment of Glioblastoma

Antiplatelet Effect of Thienopyridine ( Clopidogrel or Prasugrel ) Pretreatment in Patients Undergoing Primary Percutaneous Intervention for ST Elevation Myocardial Infarction

Disulfide bond disruption by a β3-Cys549Arg mutation in six Jordanian families with Glanzmann thrombasthenia causes diminished production of constitutively active αIIbβ3

Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

Predicting risk severity and response of fetal neonatal alloimmune thrombocytopenia

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Molecular insight into human platelet antigens: structural and evolutionary conservation analyses offer new perspective to immunogenic disorders

Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomerase

Prospective Controlled Monitoring of Hemlibra Prophylaxis Initiation in a Large Cohort of Hemophilia a Patients- Real World Data

Low Concentrations of Recombinant Factor VIIa May Improve the Impaired Thrombin Generation of Glanzmann Thrombasthenia Patients

Integrin-mediated cell adhesion requires extracellular disulfide exchange regulated by protein disulfide isomerase

Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients

Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Platelets from Calreticulin mutated essential thrombocythemia patients are less reactive than JAK2 V617F mutated platelets

Unique Disulfide Bonds in Epidermal Growth Factor (EGF) Domains of β3 Affect Structure and Function of αIIbβ3 and αvβ3 Integrins in Different Manner

Application of a clinical decision rule and laboratory assays in pediatrics: Adult heparin‐induced thrombocytopenia

Three novel mutations in the glycoprotein IIb gene in a patient with type II Glanzmann thrombasthenia

A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients

Pediatric immune thrombocytopenia: apoptotic markers may help in predicting the disease course

A Simple Two Step Approach for Diagnosis of Heparin Induced Thrmbocytopenia Using 4T Score and PaGIA Testing

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