ISTH 2020 Congress
Hemophilia and Rare Bleeding Disorders
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Abstract Number: PB1063
Bleeding Outcomes, Factor Utilization and Cost Comparisons after Switching to an Extended Half-life Product for Prophylaxis in Haemophilia A in Austria
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Abstract Number: PB1179
Blocking Tissue Factor Pathway Inhibitor (TFPI) Function Has a Therapeutic Benefit in Murine Models of Factor Deficiencies
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Abstract Number: PB0833
Bone Remodeling Alterations in Haemophilia: A Cell Biology Approach
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Abstract Number: PB0934
Cardiovascular Risk Factor Profile among North-Eastern Brazilian Adults with Haemophilia
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Abstract Number: PB1195
Characterization and Management of Patients with Mild or Moderate Hereditary Factor X Deficiency: A Retrospective Chart Review
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Abstract Number: PB1155
Characterization of Factor IX-FIAV: A Factor IX Variant that Displays Cofactor-Independent Activity
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Abstract Number: PB1159
Characterization of Neutralizing Anti-emicizumab Antibody Developed in a Hemophilia A Patient
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Abstract Number: PB1171
Clinical Characteristics of Patients with Rare Bleeding Disorders: Real-Life Data from the Netherlands (RBiN Study)
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Abstract Number: PB1094
Clinical Immunogenicity of Valoctocogene Roxaparvovec in GENEr8-1, a Phase 3 Study of AAV5-Mediated Gene Therapy Encoding Human FVIII for the Treatment of Hemophilia A
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Abstract Number: PB1080
Clinical Improvement of Haemophilic Arthropathy in a Female Pediatric Patient with Severe Hemophilia A Following Treatment with Emicizumab
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Abstract Number: PB0872
Clinical Review of Patients with Haemophilia (PwH) in a Malaysian Tertiary Center
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Abstract Number: PB0996
Clinical Validation of Population Pharmacokinetic Model for Plasma-Derived Factor VIII/VWF Comparing 3 Years Follow-up
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Abstract Number: PB0789
Coagulation and Inflammation Genes Are Differently Expressed during the Acquired Coagulation Disorder Induced by Snake Envenomation
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Abstract Number: PB0800
Coagulopathy in Pediatric Patients with Hemophagocytic Lymphohistiocytosis
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Abstract Number: PB0944
Coinfection by Hepatitis B, C and HIV in Patients with Haemophilia
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Abstract Number: PB1182
Collagen Turnover and Plasma Ascorbic Acid Levels in Patients Suspected of Inherited Bleeding Disorders Harboring Variants in Collagen-related Genes
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Abstract Number: PB1191
Combined Factor Deficiencies Rare among the Rare Bleeding Disorders among Pediatric Population, Seven Years Experience in a Tertiary Care Center of Lahore, Pakistan
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Abstract Number: PB1106
Combined Gene and Cell Therapy for the Treatment of Hemophilia A within an Implantable Therapeutic Device
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Abstract Number: PB0968
Comorbidities in Patients with Severe Haemophilia: Birth Cohort Analysis of Taiwan Society of Thrombosis and Hemostasis Database
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Abstract Number: PB1021
Comorbidities of Hemophilia & Factor XIII Deficiency Patients
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