Found: 30
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Prevalence of inhibitors and clinical characteristics in patients with haemophilia in a middle‐income Latin American country.
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- Haemophilia, 2020, v. 26, n. 2, p. 290, doi. 10.1111/hae.13951
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Hemostatic prophylaxis and colonoscopy outcomes for patients with bleeding disorders: A retrospective cohort study and review of the literature.
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- Haemophilia, 2020, v. 26, n. 2, p. 257, doi. 10.1111/hae.13954
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Activity measurements of dalcinonacog alfa.
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- Haemophilia, 2020, v. 26, n. 2, p. 346, doi. 10.1111/hae.13949
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Assessment of self‐/parent‐reported quality of life in Japanese children with haemophilia using the Japanese version of KIDSCREEN‐52.
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- Haemophilia, 2020, v. 26, n. 2, p. 243, doi. 10.1111/hae.13945
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Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand disease.
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- Haemophilia, 2020, v. 26, n. 2, p. 298, doi. 10.1111/hae.13929
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Understanding the pain profile in patients with haemophilia: Impaired descending pain inhibition as measured by conditioned pain modulation.
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- Haemophilia, 2020, v. 26, n. 2, p. 236, doi. 10.1111/hae.13939
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Opioid exposure in haemophilia patients is common and underreported.
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- Haemophilia, 2020, v. 26, n. 2, p. 251, doi. 10.1111/hae.13950
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Genetic screening of children with suspected inherited bleeding disorders.
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- Haemophilia, 2020, v. 26, n. 2, p. 314, doi. 10.1111/hae.13948
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A single centre retrospective study of low dose prophylaxis with extended half‐life factor IX for severe haemophilia B.
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- Haemophilia, 2020, v. 26, n. 2, p. 278, doi. 10.1111/hae.13936
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Reducing the effect of DOAC interference in laboratory testing for factor VIII and factor IX: A comparative study using DOAC Stop and andexanet alfa to neutralize rivaroxaban effects.
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- Haemophilia, 2020, v. 26, n. 2, p. 354, doi. 10.1111/hae.13930
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The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers.
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- Haemophilia, 2020, v. 26, n. 2, p. 306, doi. 10.1111/hae.13947
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Multicentre pharmacokinetic evaluation of rFVIII‐Fc (efmoroctocog alfa) in a real life and comparison with non‐extended half‐life FVIII concentrates.
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- Haemophilia, 2020, v. 26, n. 2, p. 282, doi. 10.1111/hae.13946
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A new paradigm for personalized prophylaxis for patients with severe haemophilia A.
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- Haemophilia, 2020, v. 26, n. 2, p. 228, doi. 10.1111/hae.13935
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Twitter and Haemophilia.
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- Haemophilia, 2020, v. 26, n. 2, p. 181, doi. 10.1111/hae.13931
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The effect of resistance exercise on strength and safety outcome for people with haemophilia: A systematic review.
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- Haemophilia, 2020, v. 26, n. 2, p. 200, doi. 10.1111/hae.13938
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Acquired Glanzmann's thrombasthenia: Diagnosis aided by platelet aggregation mixing study.
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- Haemophilia, 2020, v. 26, n. 2, p. e41, doi. 10.1111/hae.13914
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- Article
EHL‐FIX in haemophilia B carriers with FIX deficiency.
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- Haemophilia, 2020, v. 26, n. 2, p. e38, doi. 10.1111/hae.13906
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FIX potency of rFIX‐Albumin fusion protein is underestimated by one‐stage methods using silica‐based APTT reagents.
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- Haemophilia, 2020, v. 26, n. 2, p. 340, doi. 10.1111/hae.13915
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Current state of play regarding dental extractions in patients with haemophilia: Consensus or evidence‐based practice? A review of the literature.
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- Haemophilia, 2020, v. 26, n. 2, p. 183, doi. 10.1111/hae.13928
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Menstrual and obstetrical bleeding in women with inherited platelet receptor defects—A systematic review.
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- Haemophilia, 2020, v. 26, n. 2, p. 216, doi. 10.1111/hae.13927
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Antithrombotic therapy management in patients with inherited bleeding disorders and coronary artery disease: A single‐centre experience.
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- Haemophilia, 2020, v. 26, n. 2, p. e34, doi. 10.1111/hae.13904
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Eradication of factor IX neutralizing and anaphylactic inhibitors in a patient with severe haemophilia B using cyclophosphamide immune suppression and factor IX desensitization.
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- Haemophilia, 2020, v. 26, n. 2, p. e51, doi. 10.1111/hae.13926
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Clinical gait features are associated with MRI findings in patients with haemophilic ankle arthropathy.
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- Haemophilia, 2020, v. 26, n. 2, p. 333, doi. 10.1111/hae.13925
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Ligneous gingivitis: Hard to diagnose and treat.
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- Haemophilia, 2020, v. 26, n. 2, p. e49, doi. 10.1111/hae.13924
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Diagnostic work up of patients with increased bleeding tendency.
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- Haemophilia, 2020, v. 26, n. 2, p. 269, doi. 10.1111/hae.13922
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Effect of low‐dose factor VIII prophylaxis therapy on bone mineral density and 25(OH) vitamin D level in children with severe haemophilia A.
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- Haemophilia, 2020, v. 26, n. 2, p. 325, doi. 10.1111/hae.13917
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Assessment of primary haemostasis with a new recombinant von Willebrand factor in patients with von Willebrand disease.
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- Haemophilia, 2020, v. 26, n. 2, p. e44, doi. 10.1111/hae.13916
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Issue Information.
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- Haemophilia, 2020, v. 26, n. 2, p. 175, doi. 10.1111/hae.13790
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- Article
Instructions for Authors.
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- Haemophilia, 2020, v. 26, n. 2, p. 363, doi. 10.1111/hae.13789
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- Article
The bleeding score: Useful in predicting spontaneous bleeding events in adults with bleeding of unknown cause?
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- Haemophilia, 2020, v. 26, n. 2, p. e31, doi. 10.1111/hae.13775
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