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Rare bleeding disorders: diagnosis and treatment

Blood, 2015-03, Vol.125 (13), p.2052-2061

2015

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Combined Use of High-Sensitive Cardiac Troponin, Copeptin, and the Modified HEART Score for Rapid Evaluation of Chest Pain Patients

Disease markers, 2018-01, Vol.2018, p.9136971-7

2018

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Increased Risk of the APOB rs11279109 Polymorphism for CHD among the Kuwaiti Population

Disease markers, 2017-01, Vol.2017, p.6963437-8

2017

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Hemostatic alterations in COVID-19

Haematologica (Roma), 2021-05, Vol.106 (5), p.1472

2021

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An international registry of patients with plasminogen deficiency (HISTORY)

Haematologica (Roma), 2020-03, Vol.105 (3), p.554

2020

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ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission

Haematologica (Roma), 2008-02, Vol.93 (2), p.232-239

2008

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No changes of parameters nor coagulation activation in healthy subjects vaccinated for SARS-Cov-2

Thrombosis update, 2021-08, Vol.4, p.100059-100059, Article 100059

2021

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Clinical and laboratory diagnosis of rare coagulation disorders (RCDs)

Thrombosis research, 2020-12, Vol.196, p.603-608

2020

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Risk factors for inhibitor development in severe hemophilia A

Thrombosis research, 2018-08, Vol.168, p.20-27

2018

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Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

British journal of haematology, 2010-12, Vol.151 (5), p.488-494

2010

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The Effect of PAI-1 4G/5G Polymorphism and Clinical Factors on Coronary Artery Occlusion in Myocardial Infarction

Disease markers, 2015-01, Vol.2015, p.260101-8

2015

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Pathogenesis and treatment of acquired idiopathic thrombotic thrombocytopenic purpura

Haematologica (Roma), 2010-09, Vol.95 (9), p.1444-1447

2010

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Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population

Disease markers, 2015-01, Vol.2015, p.458653-6

2015

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A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking

Thrombosis research, 2014-03, Vol.133 (3), p.481-487

2014

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The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndrome

The journal of maternal-fetal & neonatal medicine, 2012-11, Vol.25 (11), p.2322-2325

2012

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Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management

Seminars in thrombosis and hemostasis, 2013-09, Vol.39 (6), p.579

2013

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Assessing Sequence Similarity between FVIII-Derived B-Cell Epitopes and Pathogen-Derived B-Cell Epitopes and the Risk of Inhibitor Development in Patients with Severe Hemophilia a

Blood, 2022-11, Vol.140 (Supplement 1), p.11282-11283

2022

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The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura

Haematologica (Roma), 2009-02, Vol.94 (2), p.289-293

2009

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Role of Chloride Ions in Modulation of the Interaction between von Willebrand Factor and ADAMTS-13

The Journal of biological chemistry, 2005-06, Vol.280 (24), p.23295-23302

2005

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Factor VIII Epitope Analysis Using a Random Peptide Phage-Display Library Approach in the Sippet Cohort

Blood, 2021-11, Vol.138 (Supplement 1), p.3176-3176

2021

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ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

Human mutation, 2010, Vol.31 (1), p.11-19

2010

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Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis

Blood, 2017-10, Vol.130 (15), p.1757-1759

2017

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Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia A

Blood, 2017-03, Vol.129 (10), p.1245-1250

2017

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IgG subclasses as biomarkers for persistence of factor VIII inhibitors in previously untreated patients with severe haemophilia A

British journal of haematology, 2021-02, Vol.192 (3), p.621-625

2021

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Real-Life Population Pharmacokinetics of Recombinant Factor XIII and Dosing Considerations for Preventing the Risk of Bleeding in Patients with FXIII Congenital Deficiency

Clinical pharmacokinetics, 2022-04, Vol.61 (4), p.505-513

2022

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Rare bleeding disorders: diagnosis and treatment

Combined Use of High-Sensitive Cardiac Troponin, Copeptin, and the Modified HEART Score for Rapid Evaluation of Chest Pain Patients

Increased Risk of the APOB rs11279109 Polymorphism for CHD among the Kuwaiti Population

Hemostatic alterations in COVID-19

An international registry of patients with plasminogen deficiency (HISTORY)

ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission

No changes of parameters nor coagulation activation in healthy subjects vaccinated for SARS-Cov-2

Clinical and laboratory diagnosis of rare coagulation disorders (RCDs)

Risk factors for inhibitor development in severe hemophilia A

Different clinical severity of first episodes and recurrences of thrombotic thrombocytopenic purpura

The Effect of PAI-1 4G/5G Polymorphism and Clinical Factors on Coronary Artery Occlusion in Myocardial Infarction

Pathogenesis and treatment of acquired idiopathic thrombotic thrombocytopenic purpura

Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population

A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking

The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndrome

Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management

Assessing Sequence Similarity between FVIII-Derived B-Cell Epitopes and Pathogen-Derived B-Cell Epitopes and the Risk of Inhibitor Development in Patients with Severe Hemophilia a

The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura

Role of Chloride Ions in Modulation of the Interaction between von Willebrand Factor and ADAMTS-13

Factor VIII Epitope Analysis Using a Random Peptide Phage-Display Library Approach in the Sippet Cohort

ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura

Genetic risk stratification to reduce inhibitor development in the early treatment of hemophilia A: a SIPPET analysis

Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia A

IgG subclasses as biomarkers for persistence of factor VIII inhibitors in previously untreated patients with severe haemophilia A

Real-Life Population Pharmacokinetics of Recombinant Factor XIII and Dosing Considerations for Preventing the Risk of Bleeding in Patients with FXIII Congenital Deficiency

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