| MP-2 | VGA039, a protein S-targeted monoclonal antibody, promotes in-vitro thrombin generation in plasma samples from subjects across a broad range of bleeding disorders, including von Willebrand disease, Hemophilia A, Hemophilia B and Hemophilia C | Kristen Jaworski | |
| PP-003 | Elucidating Pseudotumor Pathogenesis in Coagulation Disorders Through Combined Clinico-pathological and Genomic Approaches | Mariya Tomy | |
| PP-004 | Von Willebrand Disease in Tunisia: Insights from a 39-Year Bicentric Cohort | Meriem Achour | |
| PP-007 | Analysis of aPTT-Based Clot Reaction Curve in Patients With Haemophilia A, Acquired Haemophilia A and Lupus Anticoagulant – a Single Tertiary Hospital Experience | Lean Theng Ewe | |
| PP-8 | The Spectrum of the Factor 8 (f8) Defects in 106 Children with Haemophilia A (HA) living in Greece: a Single Centre Experience | Athina Dettoraki | |
| PP-010 | The Hematocrit Factor: Adjusting anticoagulants for accurate coagulation analysis | Maliha Sumbul | |
| PP-012 | Acquired Hemophilia A: Monocentric Experience of a Tunisian Center | Ghassen Saidi | |
| PO-014 | Effects of human placenta hydrolysate and thymosin alpha 1 on blood coagulation parameters in patients with hemophilia A: An ex vivo study | Ki Young Yoo | |
| MP-016 | The DivulgHEMOs Project: Advancing Hemophilia Literacy for Laypeople, Patients, and Their Families Through Social Media | Ricardo Mesquita Camelo | |
| MP-17 | Capacity building of patients to report their bleeds & treatment data through myWBDR | Hamza Qureshi | |
| PP-018 | The World Federation of Hemophilia Strategic Plan 2026–2030 | Alain Baumann | |
| PP-019 | Turning Data Into Voice: Regional Advocacy Priorities for Bleeding Disorders in the Eastern Mediterranean Region | Donna Coffin | |
| PP-022 | Evaluating the Impact of WFH Programs on Clinical & Health Care Outcomes in Pakistan: A Case Study | Donna Coffin | |
| PO-024 | From Vision to Action: National Bleeding Disorders Foundation´s Roadmap for Achieving Health Equity, Diversity, and Inclusion | LEONARD VALENTINO | |
| PP-025 | Building Organizational Resilience to Serve Bleeding Disorder Communities | Deon York | |
| PP-27 | Digital Advocacy, Legal Literacy, and Holistic Wellness: An African Hemophilia Youth Multi-Pillar Empowerment Model for Health Equity. | Pius opalakadi | |
| MP-028 | Structuring and Directing a Campaign for the Incorporation of Emicizumab for Children with Hemophilia A in Brazil | Mariana Battazza | |
| PP-029 | Establishing a National Hemophilia Helpline to Strengthen Information Access and Community Support in Pakistan | Masood Fareed Malik | |
| PP-030 | Developing a Psychosocial Toolkit for People Living with Bleeding Disorder in India. | Richa Mohan | |
| PP-34 | Fifty years of the Catalan Hemophilia Association: from advocacy to a comprehensive model of hemophilia care and psychosocial support | Patricia Cabré | |
| FP-034 | The body speaks before the child: Subjective constitution in children with hemophilia | Veronica Cerutti | |
| PP-035 | Development of a therapeutic education program on heavy menstrual bleedings (HMB) across all type of congenital bleeding disorders | Caroline ARTU DUMONT | |
| PP-038 | HTC Achievements | Ghazala Manzoor | |
| PP-039 | Experience and Challenges in Establishing a Community-Based NGO for Hemophilia Support in Pakistan | Muhammad Amar Muhammad Amar | |
| PO-041 | Empowering Bleeding Disorder in Balochistan Advocacy, Awareness and Treatment Access | Ghazala Manzoor | |
| PO-043 | Promoting Transparent Practices in the World Federation of Hemophilia´s Humanitarian Aid Program | Masood Fareed Malik | |
| PO-044 | Strengthening Community Capacity Through Youth-Led Volunteer Activities: A Case Study from Korea | Kanghoon Jeong | |
| PO-045 | Establishing the First Public-Sector Hemophilia Treatment Centre in Pakistan: A Model for Sustainable, Comprehensive Care | Masood Fareed Malik | |
| PO-047 | Improving Rural Outreach and Access to Care for People with Bleeding Disorders in Pakistan: Lessons from a Community-Based Initiative | Muhammad Amar Muhammad Amar | |
| PO-049 | Educational information for professionals at health, people with hemophilia and primary caregivers. | Laura Irene Páez Briseño | |
| PO-050 | Empowering Patients Through Awareness and Education in Bleeding Disorders: A Community-Led Approach from Pakistan | Muhammad Amar Muhammad Amar | |
| PO-052 | A STRUCTURED PATHWAY TO SUPPORT PATIENT-HEALTHCARE PROFESSIONAL PARTNERSHIP IN THERAPEUTIC PATIENT EDUCATION FOR RARE BLEEDING DISORDERS | Caroline ARTU DUMONT | |
| PO-053 | Navigating Youth Inclusion Within the Board Committee of the Hemophilia Society of Malaysia | Amierul Hakimie Luqman bin Yusli | |
| MP-054 | Assessment of Comprehensive Care for Bleeding Disorders: Insights from 10 years of Annual Global Survey data | Ellia Tootoonchian | |
| MP-055 | Advancing Shared Decision-Making in Hemophilia: Development and Contextualization of Consensus-Based Best Practice Statements | Donna Coffin | |
| MP-058 | Improving Care for Hemophilia and Other Bleeding Disorders Through Comprehensive Clinics: Perspectives from a Low-Resource Set-Up | ALEX GACHOYA | |
| PP-059 | Patient-centred Summary: Evaluating Outcomes and Follow-up Across All Severities of Haemophilia | Liz Beatty | |
| PP-060 | Addressing Stigma in Hemophilia Management: Insights from Two Tertiary Hospitals in a Low-Income Country | Abu Yousuf Md Nazim Uddin | |
| PP-062 | Synergies for Patients: A Domiciliary Delivery Program of Coagulation Factors for Hemophilia Patients in a Middle-Income Country´s Social Security Health System | Marilyn Mendoza | |
| MP-63 | Obstacles and Limitations of Care in Adolescents and Young Adults with Hemophilia | Nongnuch Sirachainan | |
| PP-064 | Humanitarian Support of the World Federation of Hemophilia: Advancing Care and Quality of Life for Individuals with Bleeding Disorders in Pakistan | Masood Fareed Malik | |
| PP-065 | Navigating the Transfer of Care in Rare Bleeding Disorders: Experiences and Needs from Adolescents and Young Adults, their Caregivers and Healthcare Providers | Greta Mulders | |
| PP-066 | From Regional Hospitals to Local Pharmacies: Evaluating Ten Years of Changes in Coagulation Factor Delivery in Estonia | Martin Kaal | |
| PP-067 | Clinical Impact of Immediate Versus Delayed Factor Replacement in the Management of Hemophilic Bleeding Episode | Usama Grewal | |
| PP-068 | Plain Language Summary: What is Extravascular Distribution of Factor IX and how does it Affect Management of Those with Haemophilia B? | Liz Beatty | |
| PP-69 | Evaluating The Effectiveness Of The Self-Bat screening Tool In Improving Early Diagnosis In A Tertiary Hospital | Abu Yousuf Md Nazim Uddin | |
| PP-071 | Tattoos: A global bleeding disorders survey | Cathy Harrison | |
| PO-077 | Advancing Evidence-Based Care: 2025–2026 Update of the WFH Living Guidelines for the Management of Hemophilia, Prophylaxis and Hemostatic Agents | Donna Coffin | |
| PO-80 | Mild Matters: A Survey of US Hematologists on the Diagnosis and Management of Individuals with Mild Hemophilia | Ming Yeong Lim | |
| PO-082 | Improving Diagnosis of Hemophilia by Use of Pedigree and Contact Tracing in Western Kenya | Nancy Midiwo | |
| PO-083 | Mindset and attitudes towards people with hemophilia A after the introduction of emicizumab prophylaxis: impressions of the biopsychosocial support team | Ricardo Mesquita Camelo | |
| PP-084 | Results from the IMPROVE project: Complex Co-inheritance of VWD Type 2N, VWD Type 1, and Mild Haemophilia A in a Large Multigenerational Family – Diagnostic and Therapeutic Implications | Anna Pavlova | |
| PP-085 | Sixth Interim Analysis of the HEM-POWR Study: Real-World Effectiveness and Safety of Damoctocog Alfa Pegol in Patients With Severe and Nonsevere Hemophilia A | Amanda Ward | |
| PP-086 | Sixth Interim Analysis of the Real-World HEM-POWR Study: Surgical Hemostasis With Damoctocog Alfa Pegol in Patients With Hemophilia A | Amanda Ward | |
| PP-087 | Galician multicenter clinical experience with emicizumab in patients with severe hemophilia a: a real-world analysis | Rebeca Guzmán | |
| PP-088 | Replacement Therapy Around Percutaneous Coronary Intervention and the Subsequent Dual Aantiplatelet Therapy Period in Hepatitis C Virus and Human Immunodeficiency Virus coinfected Hemophiliacs | Haruka Uemura | |
| PP-090 | Bridging the Gap: A Systematic Review of Modern Hemophilia Therapies and Global Inequities in Clinical Trial Participation | Nadiya Nurul Afifah | |
| PO-092 | Bleeding Complications Following Wisdom Tooth Removal for Patients with Haemophilia and von Willebrand Disease Managed Using a Tranexamic Acid Protocol | Mathew Lim | |
| PP-093 | Emicizumab Prophylaxis in Children with Hemophilia A without Inhibitors: the Brazilian Experience | Ricardo Mesquita Camelo | |
| PP-095 | Real-World Effectiveness, Safety, and Quality-of-Life Outcomes of Lonoctocog Alfa in Thai Paediatric Previously Treated Patients with Severe Haemophilia A: A Case Series | Nongnuch Sirachainan | |
| PO-096 | Physical Activity and Bleed Prevention for People With Severe Haemophilia A Treated With Once-Weekly Efanesoctocog Alfa: A Plain-Language Summary of 12-Month Interim Results From the FREEDOM Study | Nadia Gonnermann | |
| PO-97 | Exploratory Analysis from HAVEN 1–4 to Further Contextualise Injection-Site Reactions Among People with Haemophilia A Receiving Emicizumab | Helen Miller | |
| PO-098 | Bringing American Thrombosis and Hemostasis Network (ATHN) Research Opportunities to Patient-Facing Conferences: The One Drop Experience | Shelby Domino | |
| PO-099 | Adult and adolescent hemophilia patients treated with MarstacimaB: a patient Experience Registry (AMBER) and Real-World Assessment of Treatment Burden and Patient Preferences | Mankai Ju | |
| PP-102 | Therapy Adjustment in Patients with Coagulation Disorders and Myeloproliferative Neoplasms | Maria Teresa Alvarez Roman | |
| PP-104 | Prevalence of Overweight and Obesity in Hemophilia: Evidence From a Real-World Cohort in Córdoba | Monica Martinez | |
| PO-106 | BODY MASS INDEX (BMI) IN TUNISIAN PATIENTS WITH HEMOPHILIA: INSIGHTS FROM THE World Bleeding Disorder Registry (WBDR) | Ons Ghali | |
| MP-107 | The WFH Gene Therapy Registry: Early Implementation Experience and Global Collaboration | Mayss Naccache | |
| PP-108 | Universal Clinical Intelligence & Psychosocial Network: A Scalable Generalist Digital Health Ecosystem for Complex Chronic Disease Management | Ronald Mahomane | |
| PP-109 | Impact of the Socioeconomic Status of the Patient on the Management of Hemophilia A | Usama Grewal | |
| PP-110 | Public Assistance for People with Hemophilia in Brazil (PATCH) Survey: Outcome Assessment across the Brazilian Hemophilia Treatment Centers | Ricardo Mesquita Camelo | |
| PP-111 | Management of hemophilia in developping countriesThe Moroccan experience | Mohamed El khorassani | |
| PP-112 | Development of a National Web-Based Patient Registry as a Tool for Strengthening Care, Data Quality, and Health Advocacy in Pakistan | Masood Fareed Malik | |
| PP-113 | Breakthrough Bleeds Among People With Severe Hemophilia on Prophylaxis Therapy at a Tertiary Centre | Suhaila Sukiman | |
| PP-114 | Growth in use of myWBDR in Tunisia | Kaouther Zahra | |
| PP-116 | USE OF WBDR MONITORING HJHS FOR PATIENTS WITH HEMOPHILIA | Kaouther Zahra | |
| PO-117 | Public Assistance for People with Hemophilia in Brazil (PATCH) Survey: Inhibitor Screening and Diagnosis, and Immune Tolerance Induction | Ricardo Mesquita Camelo | |
| PO-118 | Public Assistance for People with Hemophilia in Brazil (PATCH) Survey: Patient Profiles, Interdisciplinary Team, and Treatment Support across the Brazilian Hemophilia Treatment Centers | Ricardo Mesquita Camelo | |
| PO-120 | Hemophilia Patient Journey study in China | Linguo Li | |
| PP-125 | Understanding Gene Editing in Hemophilia: A New WFH Education Initiative | Mayss Naccache | |
| MP-128 | The Iron Triangle of Cure: A Quantitative Risk Framework (PD, LGD, CVaR) for Securitizing Gene Therapy Supply Chains in Emerging Markets | Ronald Mahomane | |
| PP-129 | Actual Impact of Overweight and Obesity on Coagulation Factor Consumption and Healthcare Costs in Patients with Haemophilia | Hossein Motahari | |
| PP-130 | DivulgHEMOs Project: An Educational Initiative to Improve Hemophilia Knowledge in Infrequent Healthcare Providers | Ricardo Mesquita Camelo | |
| PP-133 | Establishment of Hemophilia Welfare Society Balochistan | Ghazala Manzoor | |
| PP-135 | The Holistic Health Potential Metric: A Novel Composite Measure Integrating Biomedical, Social, and Systemic Determinants | Ronald Mahomane | |
| MP-137 | Changes in hypertrophic synovium status in adult patients with severe HA receiving emicizumab prophylaxis | Ilenia Calcaterra | |
| MP-138 | Research and Single–Center Validation of a Convolutional Neural Network–Based Ultrasound Assessment Model for Hemophilic Arthropathy | Jun Li | |
| PP-140 | Comparison of Point-of-Care Ultrasonography (POCUS) With Magnetic Resonance Imaging (MRI) in Assessment of Joints in Hemophilic Arthropathy | Praveen Kumar | |
| PP-141 | Protecting Joints from the Start: Point-of-Care Ultrasound Evidence Supporting Primary Prophylaxis in Hemophilia | Mauro Dyntino | |
| PP-142 | Comprehensive musculoskeletal evaluation in hemophilia: Relationship between arthropathy and tendinopathy using HEAD-US and THD-US methods | ALVARO AUGUSTO VARGAS CARO | |
| PP-143 | Musculoskeletal Ultrasound for Joint Monitoring in Patients with Hemophilia: a Longitudinal Study | Henry Hon Wai Lam | |
| PO-147 | Spontaneous Retroperitoneal And Psoas Muscle Hematoma, With Abscess And Calcification, In Severe Hemophilia A: Challenges In The Context Of Limited Resources | Etelvina de Jesus Elija | |
| MP-148 | Diverse B-cell Responses to FVIII in Persons with Severe Hemophilia A | SHANNON MEEKS | |
| PP-150 | Inhibitors in Haemophilia A & B: UK Lived Experiences Across Life Stages | Ranjit Nagra | |
| PP-153 | Genetic and Clinical Characteristics of Haemophilia A Patients with Factor VIII Inhibitors | Kee Tat Lee | |
| PP-154 | Clinical Characteristics of Factor VIII Inhibitor Development in Children with Hemophilia A in Indonesia: Experience from a Low- and Middle-Income Country | Purnamasari Natsir Putri | |
| PP-155 | Drastic Bleed Reduction With Adjunctive Emicizumab in Immune Tolerance Induction-Refractory Haemophilia A and High-Risk Genetics: A Clinical Management Strategy | Wan Alia Amalina Binti Adenan | |
| PP-156 | Factor VIII inhibitor detection by bovine based chromogenic Nijmegan- Bethesda assay – Experience from a Specialised Coagulation Laboratory | Sitalakshmi Subramanian | |
| PP-157 | Spectrum of F8 Gene Variants in Haemophilia A Patients With Inhibitor Development | Nursaedah Abdullah Aziz | |
| PP-158 | Prevalence of Inhibitor Development in Malagasy Patients with Hemophilia: A Prospective Study | Toong Youttananukorn | |
| PP-159 | Modifiable and non-modifiable risk factors for inhibitor development in previously untreated patients with haemophilia A controlled in Venezuela National Hemophilia Center | Apsara Boadas | |
| PO-161 | Acute Compartment Syndrome in a Haemophilia A Patient With Inhibitors: A Case Report | Marwa N. Soramairy | |
| PO-162 | Hemophilia A Inhibitors in Sousse, Tunisia: First Local Insights, Diagnostic Barriers, and Management Outcomes | Ghassen Saidi | |
| PO-163 | Inhibitor testing in Hemophilia our experience at HTC from a govt. facility in North India | Savitri Singh | |
| PO-164 | Organized Gluteal Hematoma in Hemophilia A Patient with Factor VIII Inhibitors Treated with On-Demand Therapy | Salih Aksu | |
| PO-165 | Inhibitors in Hemophilia: A Challenging Complication | Maha charfi | |
| MP-168 | Utilising Thromboelastography for Predicting Bleed Risk in Patients with Mild Haemophilia A and Factor VIII Discrepant Assays | Stephanie Wong | |
| MP-169 | Long-Term Evaluation of External Quality Assessment Results for Factor VIII | Claudia van Rijn | |
| MP-170 | Bridging the Assay Gap: One more reagent for Accurate Measurement of Efanesoctocog Alfa | Angelo Claudio Molinari | |
| PP-171 | Long-term performance of Factor VIII inhibitor testing by laboratories participating in the ECAT External Quality Assessment Programme | Piet Meijer | |
| PP-172 | Long-Term Performance of Factor VIII by Laboratories of the Italian Haemophilia Centers. | Claudia van Rijn | |
| PP-173 | Strategies to correct FVIII interference on emicizumab plasma levels | RODOLFO SUELDO | |
| PP-174 | Long-term performance of Factor VIII inhibitor testing by laboratories of Italian Hemophilia Centers | Piet Meijer | |
| PP-176 | Performance Evaluation of a One-Stage Clotting Assay for Monitoring Efanesoctocog Alfa Activity: Insights from the ECAT 2024 Survey | Marika Pikta | |
| PP-177 | Improving Hematology Lab Results: Detecting Preanalytical Errors through Quality Metrics | Noorulain Fareed | |
| PP-180 | Challenges in Laboratory Assessment of Hemophilia A Patients on Emicizumab Undergoing Surgery: A Single-Center Experience from South India | Bitty Kurian | |
| PP-181 | Critical Value Matters: A Study of Critical Value Identification and Notification to clinicians in the hematology section of the Pathology Laboratory at a Tertiary Care Hospital | Noorulain Fareed | |
| PP-182 | Molecular Diagnosis of Unresolved Congenital Coagulopathies: Beyond Routine Testing | Francisco Vidal | |
| PO-184 | Efanesoctocog alfa Measurement Using Reagent Substitutions and Determining its In Vitro Temperature Stability | Geoffrey Kershaw | |
| PP-185 | Transferrin Receptor 1 as a Novel Therapeutic Target for Hemophilic Synovitis | Tsunemasa Kita | |
| MP-186 | FVIII Expression Via Non-viral Vector DNA Medicine Platform Results in Efficacious Levels of FVIII Protein and Correction of the Bleeding Phenotype in Hemophilia A Mice | Stefani Slog | |
| PP-189 | Thrombotic Events in Adult Patients With Severe Hemophilia on Emicizumab: Results of a National Study | Predrag Miljic | |
| PP-190 | Real-World Effectiveness and Safety of Emicizumab in a Cohort of 39 Pediatric Patients with Hemophilia A in Balochistan, Pakistan | Mohammad Qayyam Khan | |
| PP-192 | Advocacy on the Impact of Emicizumab on Young Lives in Mauritius | Janaki Sonoo | |
| PP-193 | THE ROLE OF EMICIZUMAB IN HEMOPHILIA PATIENTS WITH ANTI-FVIII INHIBITORS A REPORT OF 5 CASES : | Mohamed El khorassani | |
| MP-195 | Nursing Practice in the Era of Emicizumab: Five-Year Surgical Experience at the Queensland Haemophilia Centre | Alexandra Klever | |
| PP-196 | Challenges in Maintaining Employment for Hemophilia Survivors in Their forties Infected with HIV Through Blood Products and Implications for Nursing Support | Miwa Ogane | |
| PP-198 | Oral hygiene habits, sugar consumption, and dental care in children with hemostasis disorders | Laura Beatriz Isidro-Olán | |
| PO-199 | Evaluation of underlying etiology and therapeutic challenges of Recurrent Gingival Hemorrhage in Severe Hemophilia A: A Case Report from a Developing Country | Salsa Makruf | |
| MP-200 | Standard Half-Life (SHL) and Extended Half-Life (EHL) FVIII in Major Orthopedic Surgery: Evidence from Real-World Experience. | ezio.zanon@unipd.it ezio.zanon@unipd.it | |
| PP-201 | Awareness of Hemophilic Patients Regarding Potential Orthopedic Abnormalities of Target Joints | Usama Grewal | |
| PP-203 | Myositis Ossificans as a Complication of Haemophilia: A 20-year retrospective case series | Adam Hussain | |
| PP-204 | Correlation of FVIII:C and Joint Health in Korean Patients with Hemophilia A | Hong Hoe Koo | |
| PP-205 | Pediatric Severe Hemophilia with Ankle Hemophilic Arthropathy: Microfracture with Cartilage Repair- Surgical Case Study | Elia Fong | |
| PP-206 | Orthopaedic Management of Complex Haemophilic Arthropathy of the Ankle Joint | Adam Hussain | |
| PP-207 | Managing Complex Haemophilia A Presentations in Low-Resource Settings: A Two-Case Series Highlighting Multisystem Challenges and Delayed Access to Therapy | Erick Ayaye | |
| PO-208 | Prophylaxis vs On-Demand Treatment: Ripple Effects After Many Years! | Waleed Grewal | |
| PO-209 | A proposed classification for end stage hemophilic knee arthritis requiring Total knee replacement with suggested treatment/ constraint options. | Sandeep Albert | |
| PO-210 | Management of Hemophiliac Arthritis of Target Joints | Usama Grewal | |
| PO-211 | Establishing a Multidisciplinary Model for Musculoskeletal Surgery in Severe Hemophilia within a Resource-Limited Setting | Bhaskar Pant | |
| PO-213 | A retrospective study of Radiosynovectomy on Target Joints in Haemophilia from a Tertiary Hospital | Shin Yen Yeam | |
| PO-214 | Surgical Outcomes in Extremity Hemophilic Pseudotumors | Sanjana Bose | |
| PP-215 | Determinants of Central Sensitization in Hemophilic Arthropathy: A Multicentre Analysis of Psychosocial and Joint-Related Predictors. | Ruben Cuesta-Barriuso | |
| PP-216 | Effectiveness and Tolerability of a Topical Emulgel Containing Glucosamine Sulphate, Chondroitin Sulphate, Curcumin, Boswellia Serrata, Ginger, Oil of Wintergreen, and Menthol in Pediatric Haemophilic Arthropathy | Pamela Narayan | |
| MP-218 | Long-Term Outcomes and Inhibitor Relapse Following Immune Tolerance Induction in Severe Hemophilia A Children with Inhibitors: A Prospective Multicenter Study | Runhui Wu | |
| PP-219 | The Hemophilia Health Journey: Exploring the Experiences and Unmet Care Needs of Young Children with Hemophilia and their Caregivers | Caroline Mussert | |
| PP-220 | A Single Paediatric Centre Experience in Immune Tolerisation Induction (ITI) for Paediatric Severe Haemophilia A Patients with Inhibitors on Subcutaneous Emicizumab | Chiew Ying Lim | |
| PP-221 | Clinical Profile of Children with Factor XI Deficiency in Singapore | Nur Insyirah Abdul Kadir | |
| PP-222 | Pharmacokinetic Parameters Related Bleeding Outcomes of Hemophilia A Treated with Low Dose Prophylaxis Treatment in Thailand Under National Health Security Office Scheme in Thailand | Bunchoo Pongtanakul | |
| PP-223 | Novel Variants in Hemophilia A Patients: Report from a Referral Hemophilia Treatment Centre in Indonesia | Fitri Primacakti | |
| PP-225 | Clinical Profile of Hemophilia Children Admitted to a Limited-Resource Hospital in West Nusa Tenggara, Indonesia: A Cross-Sectional Study | Yudhi Kurniawan | |
| PP-226 | Recurrent Hemophilic Pseudotumor in Mild Hemophilia A with Neurofibromatosis Type 1: Experience from a Low- and Middle-Income Country | Purnamasari Natsir Putri | |
| PP-227 | Paediatric Haemophilia B in Northern Peninsular Malaysia: A Descriptive Analysis of Patient Profiles and Outcomes | Chee Enn Han | |
| PP-228 | Safe Childhood: Helping Children With Hemophilia A Stay Active and Confident | Aamir Aslam Awan | |
| PP-229 | Epidural Hematoma on the Left Frontoparietotemporal Region in a Child with Newly Diagnosed Severe Hemophilia A: A Case Report | Salsa Makruf | |
| MP-232 | Efficacy and Safety of Low-Load Blood Flow Restriction Training in Hemophilic Ankle Arthropathy: A Multicenter Randomized Clinical Trial | Rubén Cuesta-Barriuso | |
| PP-233 | Recreative Sport, Joint Health, and Musculoskeletal Power in Children and Young People with Haemophilia | Carlos Cruz-Montecinos | |
| PP-235 | Ten Years of Multidisciplinary Rehabilitation Check-ups for People with Hemophilia in Japan: Long-Term Survivors of HIV Acquired from Historically Contaminated Blood Products | Fujitani Junko | |
| PP-236 | A comparison of patients presenting with musculoskeletal issues to the bleeding disorder rheumatology clinic 10 years apart | Abi Polus | |
| PP-237 | The Effects of Physical & Mental Health Rehabilitation Program(PMHRP) in post operative periods for hemophilic arthritis | Won-Sook Bak | |
| PP-238 | A Prospective Ultrasound Framework for Physiotherapists Working in Haemophilia Care | James Cartwright | |
| PP-241 | Safety and Efficacy of Physiotherapy in Patients with Severe Hemophilia A Treated with Emicizumab: A Prospective Polish Multicenter Study | Ewa Stefanska-Windyga | |
| PO-243 | Role of Physiotherapy to Rehabilitate a Person with Hemophilia Induced Foot Drop: A Case Study | Easmin Ara Doly | |
| PO-246 | Individualized Physiotherapy Program Combining Manual Therapy and Exercise Improves Musculoskeletal System, Cardiopulmonary Endurance and Quality of Life in Patients With Hemophilia A | Wan-Jung Kao | |
| PO-247 | Neuromotor Reprogramming in Hemophilia: Preliminary Experience Using the Allyane Method | Mauro Dyntino | |
| PO-248 | Point of Care Ultrasound Use Among Australian Physiotherapists Working with People with Bleeding Disorders | Abi Polus | |
| MP-249 | Long-term outcome with emicizumab prophylaxis for haemophilia A in China and efficacy prediction using machine learning | Yuan Xu | |
| MP-250 | Efficacy of Low-Dose Emicizumab Prophylaxis in Hemophilia A: A Systematic Review and Meta-Analysis | April Joy Ong | |
| PP-251 | Real-World Efficiency of EHL FIX Prophylaxis in Hemophilia B | Olga Benítez Hidalgo | |
| PP-253 | Real-World Experience with Emicizumab Prophylaxis from a single Canadian Tertiary Care Center | Areeb Hassan | |
| PP-255 | Pediatric Cohort Treated With rIX-FP (Idelvion): Real-World Analysis of Efficacy, Safety, PK Improvement and Resource Utilization | BOLIVAR LUIS DIAZ JORDAN | |
| PP-256 | The Role of Low dose Emicizumab Prophylaxis in Improving PedHAL Domains and Clinical Outcomes in Children with Hemophilia: An insight from a low-middle income country. | Shigy Francis | |
| PP-257 | Level of Knowledge of Hemophilia Patient´s Families in Implementing Prophylactic Therapy at the Hemophilia Treatment Center Ulin General Hospital , Banjarmasin, Indonesia | Wulandewi Marhaeni | |
| PP-259 | Determinants of Adherence to Clotting Factor Prophylaxis in Adolescent and Adult Men with Hemophilia | Alice Sacramento | |
| PP-261 | Management for Hemophilia A Pediatric Patients without Inhibitors Receiving Nationwide Emicizumab Prophylaxis | sanikarn nakrong | |
| PP-262 | New Confidence Through Modern Prophylaxis: Community Experiences With Emicizumab in Hemophilia A | Aamir Aslam Awan | |
| PP-263 | Bleeding Outcomes >3 Years After Discontinuing Emicizumab Among Persons With Hemophilia A in a Low-Resource Setting: Experience From Moi Teaching and Referral Hospital, Kenya | Everlyn Aliwa | |
| MP-267 | "Hemophilia explained for children": A psychosocial approach through storytelling | Patricia Cabré | |
| MP-268 | Tea Party Care in the Hemophilia Community: A Psychosocial Healing Program for Parents of Children with Hemophilia | Jeong Sik Hwang | |
| MP-269 | Patient-Reported Outcomes on Artificial Intelligence Use in Hemophilia: a Psychometric Evaluation | Cindy Komar | |
| PP-271 | Mental Health Needs Assessment Among People With Hemophilia in Nepal: A Mixed- Methods Study | Toong Youttananukorn | |
| PP-272 | Evaluating the World Federation of Hemophilia´s Shared Decision-Making Tool: Insights from a Multi-Group Impact Study | Donna Coffin | |
| PP-273 | Emotional Burden and Marginalization in Individuals with Bleeding Disorders | Midhat Khalid | |
| PP-275 | The Importance of the Psychosocial Approach in the Healthcare Team: Current Reality and Future Perspectives | Silvina Grana | |
| PP-276 | Advancing Mental Health and Substance Use Care Accessibility for Individuals With Bleeding Disorders: A United States Multi-State Outreach and Champion Facility Identification Model | Shanthi Hegde | |
| PP-278 | Navigating Life With Bleeding Disorders: Understanding the Lived Psychosocial Experiences of Youth | Midhat Khalid | |
| PP-280 | Psychosocial well being and exercise participation of patients with Haemophilia and the carers in Hong Kong | Henry Hon-Wai Lam | |
| PP-281 | Feasibility and Engagement of an Online CBT-Based Group Intervention for Adolescents with Haemophilia | Anna-Maria Tsilia | |
| PP-282 | Emotional Impact of Hemorrhagic Disorders on Mexican Female Caregivers: Prevalence of Anxiety and Depression | Ezequiel Martinez Martinez | |
| PP-283 | Neurobiological Perspectives on Hemophilia: A Review of Neurological, Cognitive, and Psychosocial Interactions | Ferose Pallimanhayalil | |
| PP-284 | Beyond Carriers: Promoting Recognition, Diagnosis, and Psychosocial Inclusion for Women with Bleeding Disorders in Korea | Jeong Sik Hwang | |
| PP-287 | Comparison of psycho-social difficulties faced by haemophilia patients with and without HIV/AIDS | Tomie Fujii | |
| PP-288 | Creating a Children´s Book as a Tool for Education and Support | Darian Smith | |
| PP-290 | Innovations in Child Life Services for Hemophilia Care in Kenya: Enhancing Psychosocial Support and Treatment Compliance for Pediatric Patients Living with Hemophilia | Bilha Nyaboke Omari | |
| PP-291 | Balancing Hemophilia Care and Cultural Practices:Psychosocial and Clinical Outcomes of Circumcision with Optimized Factor Therapy | AJAI THOMAS | |
| PP-292 | Ibero-American Psychosocial Group: A Collaborative Network in Development | Silvina Graña | |
| PP-295 | New educational strategies for individuals with hemophilia and autism | Tongpil Min | |
| PP-296 | Hemophilia and autism: where do challenges come from? | Gavin Min | |
| PP-297 | A Study on Development of RAG-based Psychological Counseling Support System via Analysis of Unmet Counseling Needs in Hemophilia Patients | Jihun Chang | |
| PO-298 | Bleeding in Silence: A Young Man´s Battle for Identity, Dignity, and Hope with Severe Hemophilia A | Masood Fareed Malik | |
| PO-300 | Personal Coping Pathways and Psychosocial Resilience in a Person With Hemophilia | Masood Fareed Malik | |
| MP-303 | Psychological Well-being in Primary Caregivers of People with Coagulopathies | Ezequiel Martinez Martinez | |
| MP-305 | Patient-Reported and Clinical Outcomes in Persons with Severe Hemophilia (PwSH) Treated Within vs. External to U.S. Hemophilia Treatment Center Network Clinics: An Update from the CHESS US Study | Randall Curtis | |
| MP-306 | Hemophilia Life Stages and Changes Global Survey of People with Hemophilia, Caregivers, and Hematologists: Patient Experience According to Disease Severity and Gender | Kim Isenberg | |
| MP-307 | Psychological Burden and Quality of Life of Mothers of Hemophiliac Children: A study of 69 cases | Mohamed El khorassani | |
| PP-309 | WBDR RSP Series Part 1/6: Beyond Patient Registry – Demonstrating Multifunctional WBDR Value Across Six Domains (32 Research Support Program Projects, 2018–2023) | Toong Youttananukorn | |
| PP-310 | WBDR RSP Series Part 2/6: Generating Clinical Evidence That Informs Policy – Four Focused Research Areas from 32 RSP Projects (2018–2023) | Toong Youttananukorn | |
| MP-311 | WBDR RSP Series Part 3/6: Diagnosis Evidence– Findings From Research Projects Under the WFH WBDR Research Support Program (2018–2023) | Toong Youttananukorn | |
| PP-312 | WBDR RSP Series Part 4/6: Quality-of-Life Evidence – Findings From Research Projects Under the WFH WBDR Research Support Program (2018–2023) | Toong Youttananukorn | |
| PP-313 | WBDR RSP Series Part 5/6: Prophylaxis Evidence - Findings From Research Projects Under the WFH WBDR Research Support Program (2018–2023) | Toong Youttananukorn | |
| PP-314 | WBDR RSP Series Part 6/6: Underserved Populations (WGBD/VWD) Evidence - Findings From Research Projects Under the WFH WBDR Research Support Program (2018–2023) | Toong Youttananukorn | |
| PP-315 | Insights into Physical Function and Treatment Experience with Mim8: Patient Cases from the FRONTIER Trials | Jayson Tang | |
| PP-316 | Patient-Reported Outcomes in Hemophilia in Kosovo: Results from the PROBE Questionnaire | Dawn Rotellini | |
| PP-317 | The Quality of Life of Hemophilia A Patients Accessing Treatment Services | Toong Youttananukorn | |
| PP-318 | Long-Term Treatment Adherence Decline in Pediatric Hemophilia Patients Receiving Extended Half-Life Therapies: A Cross-Sectional Study in South Korea | Harim Kim | |
| PP-319 | Assessing the Change in Bleeding Rates and Related Clinical Outcomes in Haemophilia Patients Before and After Introducing Humanitarian Aid Clotting Factor Concentrates in Malawi | Francis Mkwenembera | |
| PP-320 | Real-World Effectiveness and Patient-Reported Burden of Pharmacokinetic-Guided Individualized Prophylaxis in Chinese Hemophilia A Patients | Shaoyu Yin | |
| PP-321 | Health-Related Quality of Life among Adults with Haemophilia in Southern Nigeria | Toong Youttananukorn | |
| PP-322 | Adapting the Patient Reported Outcomes Burdens and Experiences (PROBE) Study to Measure Quality of Life in People with von Willebrand Disease (VWD) | Elizabeth Clearfield | |
| PP-323 | Mapping the Journey of Caregivers and Patients with Hemophilia A and B in Brazil | Indianara Galhardo | |
| PP-324 | Parental Experience of Hemophilia Diagnosis Disclosure in Morocco :A Mixed-Methods Study on Communicational Quality and Psychosocial Impact | Mohamed El khorassani | |
| PP-325 | Quality of life assessment in parents of infants with severe hemophilia A without inhibitors after emicizumab prophylaxis | Canan Albayrak | |
| PP-326 | Empowering Movement in Hemophilia: A Medically Supervised Trekking Experience | Carlos Kolker | |
| PP-327 | Mapping the Journey of Caregivers and Patients Under 6 Years Old with Hemophilia A in Brazil | Mariana Battazza | |
| PP-329 | Impact of Hemophilia on Quality of Life and Self-Esteem in Adolescents and Young Adults in South India | Ferose Pallimanhayalil | |
| PP-331 | Evaluation of the Quality of Life of Hemophiliac Patients Under Prophylactic Treatment in Cameroon | Toong Youttananukorn | |
| PP-332 | Assessment of Joint Arthropathy by FISH and Pain Scoring in Hemophilia Patients: Experience from Pakistan | Munira Borhany | |
| PP-333 | Emicizumab Prophylaxis and Its Impact on Bleeding Control, Joint Health, and Psychosocial Well-Being in Hemophilia A | Ayisha Imran | |
| PO-334 | Satisfaction Towards A Multidisciplinary Service on Haemophilia Care | YI JING LEE | |
| PO-337 | Increasing Patient and Family Knowledge Regarding the Joint Health of Hemophilia Patients: Educational Intervention at Hemophilia Treatment Center Ulin General Hospital, Banjarmasin, Indonesia | Ratih Kumala Sari | |
| PO-339 | Impact of Genetic Counseling on Prevention of Factor VII Deficiency in a family from Pakistan. | Lubna Zafar | |
| PO-342 | Assessment of Quality of Life in People with Hemophilia on Coagulation Factor Prophylaxis in Brazil | Ricardo Mesquita Camelo | |
| PP-344 | Factor XIII Deficiency: Clinical features and Management Approaches from a Specialized Adult Haemophilia Treatment Centre | Kara Cordiner | |
| PP-346 | Hereditary Severe Factor X Deficiency in Childhood: Single Centre Experience at Evelina London Children´s Hospital | Jayanthi Alamelu | |
| PP-347 | A Sticky Situation: An Illustrated Review of Glanzmann´s Thrombasthenia | Shanthi Hegde | |
| PP-349 | Development of A Global Registry: The Glanzmann Thrombasthenia Real-World Insights Research Study | Amy Owen-Wyard | |
| PP-351 | Acquired Hemophilia A in a Resource-Limited Setting: Demographic Profile and Real-World Outcomes From a Multi-Centre Retrospective Study | Rema Ganapathi | |
| PP-352 | Susoctocog Alfa for Bleeding Control in High-Titer Acquired Hemophilia A: A Case Series of Four Patients | JAE JOON HAN | |
| PP-353 | Acquired deficiency of vitamin K dependent factors: an alarming increase in cases. Experience in Banco Municipal de Sangre DC, Caracas | Apsara Boadas | |
| PP-354 | Rare Bleeding diosrders - Our experience | Sitalakshmi Subramanian | |
| PO-356 | A Challenging Surgery In a Child with Inherited FVII Deficiency and a Huge Nasopharyngeal Angiofibroma | Aysegul Unuvar | |
| PO-358 | Prophylaxis for Inherited Deficiency of Factor X: A Systematic Review | Ricardo Mesquita Camelo | |
| PO-359 | Proposed Diagnostic Algorithm for Rare Bleeding Disorders | Veronica Arrieta | |
| PP-360 | Optimization of Clotting Factor Concentrates Use During Circumcision in People with Hemophilia: A Retrospective Analysis from a Low-Middle Income Country. | Shigy Francis | |
| PP-361 | Perioperative Management With Lonoctocog Alfa (Afstyla) in Hemophilia A: Real-World Surgical Experience | Olga Benítez Hidalgo | |
| PP-362 | Surgical Management in Hemophilia Patients Receiving Efmoroctocog Alfa | Goksel Leblebisatan | |
| PP-363 | Expanding Surgical Boundaries in Severe Hemophilia A: Successful Orthognathic Correction Using PK-Guided Extended Half-Life FVIII in a Middle-Income Country | Eileen Viviana Fonseca | |
| PO-365 | Perioperative Management and Surgical Outcomes in Patients With Inherited Bleeding Disorders in a Public Sector Hospital: The Pakistan Institute of Medical Sciences Experience | Farwa Sijjeel | |
| PO-366 | Intussusception Secondary to Meckel´s Diverticulitis: A Rare and Life-Threatening Complication in an Infant with Hemophilia A | Serap Karaman | |
| PP-370 | Pilot Study Exploring the Lived Experiences of Adolescents and Adults with von Willebrand Disease Treated with VGA039 and Their Families in the VIVID-3 Phase 1/2 Clinical Study | Kristen Jaworski | |
| PO-371 | Low-Dose Emicizumab Prophylaxis in Severe Hemophilia A: A Trial in Progress Evaluating Feasibility and Accessibility in a Resource-Limited Setting | Ayisha Imran | |
| MP-372 | Plasma-Derived VWF/FVIII Prophylaxis in Children Under 6 With VWD: First Results From WIL-33 | Akshat Jain | |
| MP-373 | Pregnancy Outcomes in Women with Von Willebrand Disease: A Statewide Cohort Study | Ming Y Lim | |
| MP-374 | Recombinant von Willebrand Factor, Vonicog alfa: United Kingdom experience of its use in children under 18 years of age | Jayanthi Alamelu | |
| MP-375 | Clinical Spectrum, Subtype Distribution, And Treatment Outcomes In Von Willebrand Disease: A Prospective Study From A Hemophilia Treatment Center In Pakistan | Munira Borhany | |
| PP-379 | Expanding the PIVOT-vWD Programme: An International Patient-Driven Study to Capture the Impact, Voice, and Outcomes of von Willebrand Disease | George Morgan | |
| PP-380 | Pregnancy Outcomes and Hemostatic Management in Women with Von Willebrand Disease: A Single-Center Experience | Chin Sheng Ting | |
| PP-382 | Successfully Searching to See Type 1C von Willebrand Disease | Karen Sims | |
| PP-383 | Bridging the Diagnostic Gap: Development and Validation of a Localized Screening Tool for Von Willebrand Disease in a Taiwanese Cohort | Chun-Hui Chiao | |
| PP-384 | Von Willebrand Disease and prophylactic treatment | Ons Ghali | |
| PP-385 | Managing Type 3 von Willebrand Disease Complicated by Anti-VWF Alloantibodies: A Therapeutic Challenge | Wafa Chenbah | |
| MP-386 | Global Utilisation and Impact of VWDtest.com: A Multilingual Digital Platform to Improve Awareness and Early Identification of von Willebrand Disease | Fernando F. Corrales-Medina | |
| MP-388 | They´re Missing: The Underrepresentation of Women and Girls with Hemophilia in the WBDR | Pamela Dakik | |
| MP-389 | Demographic and Socioeconomic Characteristics of Females in the Community Voices in Research Registry | Paxton G. Mills | |
| MP-390 | Assessment of joint health using HEAD-US scores among asymptomatic mothers of hemophilia/Familial Mediterranean fever patients and women with Type 3 von Willebrand disease | ZÜHRE KAYA | |
| MP-391 | Strengthening Diagnostics and Patient Care for Women and Girls With Bleeding Disorders Through International Capacity-Building and Twinning Programme | Bitty Kurian | |
| MP-394 | Bleeding Profile and Health Related Quality of Life among Females Living with Bleeding Disorders: A Single-Centre Observational study. | Rema Ganapathi | |
| MP-395 | Inherited Bleeding Disorders in Women: A 15 year cohort review from a single comprehensive center in Australia | Kara Cordiner | |
| MP-396 | Females Affected by Hemophilia A; Data From the U.S. 8CHECK Program | Barbara Konkle | |
| PP-397 | Perceived Health Status in Women with haemophilia and Carriers | Carla Daffunchio | |
| PP-398 | Improving Diagnosis and Treatment of Women with VWD in Pakistan: A Two Phase Analysis Using WBDR Data and Shared Decision Making Tools | Tahira Zafar | |
| PP-399 | Advancing Global Data Collection for Women with Bleeding Disorders: Early Insights from the PROBE WBD Module | Dawn Rotellini | |
| PP-400 | Unraveling Pathogenic Variants in the F8 Gene in Females with Mild Hemophilia A and Asymptomatic Carriers: Detecting Compound and Double Heterozygous | Yasser Vega | |
| PP-403 | Cross-cultural Adaptation and Reliability of the Self-administered ISTH Bleeding Assessment Tool | Sowmya Nayak | |
| MP-405 | Bleeding Profiles and ISTH-BAT Assessment in Women and Girls with Hemophilia: Insight from an Indonesian Referral Center | Fitri Primacakti | |
| PP-409 | Opportunities at Birth: Postpartum Hemorrhage as an Indicator for Early Hemophilia Screening in Low- and Middle-Income Countries | Maureen Kiio | |
| PP-410 | Becoming Stronger in the Bleed: A Phenomenological Case of a Young Pakistani Nurse Living With Severe Von Willebrand Disease Type 3 | wajiha javaid | |
| PO-413 | Gendered Marital Challenges for Girls with von Willebrand Disease in Pakistan | wajiha javaid | |
| PP-417 | Surgical synovectomy in moderate to severe Haemophilic arthropathy - a systematic review | Adam Hussain | |
| PP-420 | Wiskott-Aldrich Syndrome Case Series and Novel Whole Blood Exchange Transfusion | Walter Kelley | |
| PP-421 | Successful Utilisation of Low Dose Emicizumab in the Bleeding Management of Acquired Haemophilia; A Single Center Experience | Veena Selvaratnam | |
| PP-422 | Microarchitectural Bone Deterioration Despite Preserved Bone Mineral Density in Persons with Hemophilia A | Prisha Nankana | |
| PP-423 | Hemophilia treatment and Joint Health: A Colombian Hemophilia Cohort Study | Jose Santacruz-Arias | |
| PP-425 | Diagnostic Reassessment of a Congenital Bleeding Disorder From Suspected Factor X Deficiency to von Willebrand Disease | Elen Avetisyan | |
| PP-426 | Access to Care, Registry Quality, and Socioeconomic Barriers among People with Hemophilia in Uttar Pradesh, India: A Mixed-Methods Evaluation across Eight Treatment Centers | Prisha Nankana | |
| PP-428 | Bridging the Gap: Enhancing Pediatric to Adult Bleeding Disorder Care Transitions with Multidisciplinary SmartPhrases | Denise Lowery | |
| PP-429 | Severe Inhibitor Hemophilia A With Refractory Gastrointestinal Bleeding, Massive Transfusion Requirement, and Multisystem Complications: A Case Report | Anna Stepanyan | |
| PP-430 | A novel chemiluminescent microfluidic thrombin generation assay detects in vivo aPCC effects with assay-specific sensitivity to accumulated prothrombin levels | Aernoud Bavinck | |
| PO-433 | Perception and Practice of Shared Decision-Making in Hemophilia Care in China: Interim Results from a Multicenter Survey | Karina Chin Po Hsu | |
| PP-434 | Spectrum of F8 Gene Variants in a Multi-Ethnic Cohort of Malaysian Haemophilia A Patients | Yuslina Mat Yusoff | |
| PP-436 | Epidemiological Landscape and Gender Equity in a Colombian Coagulation Disorder Program | Jose Santacruz-Arias | |
| PP-437 | Bolar Provisions as a Legal Mechanism for Health Equity in Hemophilia: A Case Study on Emicizumab | Tirsa M. Carcamo Bonilla | |
| PO-440 | Impact of Joint Health on Quality of Life in Haemophilia Patients Receiving On-Demand Therapy in Indonesia | Muhammad Hakim Abyantoro | |
| PO-441 | Strengthening Hemophilia Care Through Patient Advocacy and Community-Led Initiatives in Khyber Pakhtunkhwa, KP, Pakistan | Syed Shabistan | |
| PO-442 | Low dose subcutaneous protein C concentrates in a Child with homozygous protein C deficiency | Yee Yee Yap | |
| PO-443 | Circumcision in Three Boys With Severe Haemophilia A Without Inhibitors Using Standard Factor VIII Replacement: A Case Series | Jihane Layla Azzi | |
| PO-444 | Bloodless arthroplasty surgery in patients with bleeding disorders | Yee Yee Yap | |
| PO-445 | Surgical Intervention in Von Willebrand Disease: A Single Center Experience | MEHMET CAN UGUR | |
April 19-22, 2026 Kuala Lumpur

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