Works matching IS 13518216 AND DT 2025 AND VI 31 AND IP 1
Results: 21
Genetic Analysis and Reproductive Interventions for Two Rare Families Affected by Severe Haemophilia A.
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- Haemophilia, 2025, v. 31, n. 1, p. 148, doi. 10.1111/hae.15140
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Modulation of Haemostatic Balance in Combined von Willebrand Disease and Antithrombin Deficiency: A Comprehensive Family Study.
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- Haemophilia, 2025, v. 31, n. 1, p. 140, doi. 10.1111/hae.15147
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Cross‐Cultural Translation of the Adolescent Menstrual Bleeding Questionnaire (AMBQ).
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- Haemophilia, 2025, v. 31, n. 1, p. 118, doi. 10.1111/hae.15145
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Mortality in Haemophilia Patients in India: A National Cohort Study.
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- Haemophilia, 2025, v. 31, n. 1, p. 132, doi. 10.1111/hae.15143
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Repeated Radiosynovectomy in Haemophilia: Revealing Long‐Term Effectiveness and Safety.
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- Haemophilia, 2025, v. 31, n. 1, p. 156, doi. 10.1111/hae.15142
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Successful Orthopaedic Surgeries With World Federation of Haemophilia Humanitarian Aid Program in Resource‐Limited Settings.
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- Haemophilia, 2025, v. 31, n. 1, p. 162, doi. 10.1111/hae.15141
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Low‐Dose Emicizumab Versus Low‐/Intermediate‐Dose Factor VIII Secondary Prophylaxis for Noninhibitor Haemophilia A Patients With Severe Bleeding Phenotype.
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- Haemophilia, 2025, v. 31, n. 1, p. 122, doi. 10.1111/hae.15146
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Research Letter: Patient Attitudes Towards Haemophilia Gene Therapy at a US Haemophilia Treatment Center.
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- Haemophilia, 2025, v. 31, n. 1, p. 166, doi. 10.1111/hae.15139
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Pain‐Related Quality of Life Outcomes in People With Haemophilia A Receiving Emicizumab: A Post Hoc Analysis of the HAVEN 1, 3 and 4 and STASEY Studies.
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- Haemophilia, 2025, v. 31, n. 1, p. 87, doi. 10.1111/hae.15134
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Giving Choice a Voice: Commentary on Development of the World Federation of Hemophilia Shared Decision‐Making Tool.
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- Haemophilia, 2025, v. 31, n. 1, p. 5, doi. 10.1111/hae.15133
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Real‐World Data on Patients With Acquired Haemophilia A in Japan Undergoing Rehabilitation or With Low Activities of Daily Living Scores: The ORIHIME II Study.
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- Haemophilia, 2025, v. 31, n. 1, p. 99, doi. 10.1111/hae.15132
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Moderate haemophilia A: Recommendations from a Spanish panel of experts.
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- Haemophilia, 2025, v. 31, n. 1, p. 39, doi. 10.1111/hae.15110
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Efficacy and safety of recombinant activated factor VII in Glanzmann thrombasthenia: A systematic literature review.
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- Haemophilia, 2025, v. 31, n. 1, p. 7, doi. 10.1111/hae.15130
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Assessing the factors affecting the accessibility of primary dental care for people with haemophilia.
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- Haemophilia, 2025, v. 31, n. 1, p. 69, doi. 10.1111/hae.15124
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Challenges in the diagnosis and management of patients with rare coagulation disorders in Lebanon and consequences of a social and economic crisis.
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- Haemophilia, 2025, v. 31, n. 1, p. 63, doi. 10.1111/hae.15123
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A phase 1/2 safety and efficacy study of TAK‐754 gene therapy: The challenge of achieving durable factor VIII expression in haemophilia A clinical trials.
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- Haemophilia, 2025, v. 31, n. 1, p. 108, doi. 10.1111/hae.15121
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Effects of physical therapy on health‐related quality of life in patients with haemophilia: A systematic review and meta‐analysis.
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- Haemophilia, 2025, v. 31, n. 1, p. 16, doi. 10.1111/hae.15120
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UKHCDO gene therapy taskforce: Guidance for implementation of haemophilia gene therapy into routine clinical practice for adults.
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- Haemophilia, 2025, v. 31, n. 1, p. 26, doi. 10.1111/hae.15125
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Bleed treatment with eptacog beta (rFVIIa) results in a low incidence of rebleeding in adult and adolescent patients with haemophilia A or B with inhibitors.
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- Haemophilia, 2025, v. 31, n. 1, p. 78, doi. 10.1111/hae.15109
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Development and validation of the Child Hemophilia Treatment Experience Measure: A new observer‐reported outcome measure.
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- Haemophilia, 2025, v. 31, n. 1, p. 48, doi. 10.1111/hae.15102
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Issue Information.
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- Haemophilia, 2025, v. 31, n. 1, p. 1, doi. 10.1111/hae.15043
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- Article