Works matching IS 13518216 AND DT 2020 AND VI 26 AND IP 1
Results: 33
Laboratory measurement of factor replacement therapies in the treatment of congenital haemophilia: A United Kingdom Haemophilia Centre Doctors' Organisation guideline.
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- Haemophilia, 2020, v. 26, n. 1, p. 6, doi. 10.1111/hae.13907
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A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non‐pathogenic gene variants.
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- Haemophilia, 2020, v. 26, n. 1, p. e26, doi. 10.1111/hae.13898
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An overview of turoctocog alfa pegol (N8‐GP; ESPEROCT<sup>®</sup>) assay performance: Implications for postadministration monitoring.
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- Haemophilia, 2020, v. 26, n. 1, p. 156, doi. 10.1111/hae.13897
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Measuring the impact of changing from standard half‐life (SHL) to extended half‐life (EHL) FVIII prophylaxis on health‐related quality of life (HRQoL) in boys with moderate/severe haemophilia A: Lessons learned with the CHO‐KLAT tool
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- Haemophilia, 2020, v. 26, n. 1, p. 73, doi. 10.1111/hae.13905
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Evaluation of pre‐analytic heat treatment protocol used in the CDC Nijmegen‐Bethesda assay for heat inactivation of extended half‐life haemophilia treatment products.
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- Haemophilia, 2020, v. 26, n. 1, p. e28, doi. 10.1111/hae.13901
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von Willebrand Disease and other hereditary haemostatic factor deficiencies in women with a history of postpartum haemorrhage.
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- Haemophilia, 2020, v. 26, n. 1, p. 97, doi. 10.1111/hae.13900
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Rotational thromboelastometry can predict the probability of bleeding events in a translational rat model of haemophilia A following gene‐based FVIIa prophylaxis.
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- Haemophilia, 2020, v. 26, n. 1, p. 164, doi. 10.1111/hae.13899
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Laboratory coagulation tests and emicizumab treatment A United Kingdom Haemophilia Centre Doctors' Organisation guideline.
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- Haemophilia, 2020, v. 26, n. 1, p. 151, doi. 10.1111/hae.13903
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Inhibitor epidemiology and genetic‐related risk factors in people with haemophilia from Côte d'Ivoire.
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- Haemophilia, 2020, v. 26, n. 1, p. 79, doi. 10.1111/hae.13902
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Excessive breakthrough bleeding in haemophilia B patients on factor IX‐albumin fusion protein prophylactic therapy: A single centre case series.
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- Haemophilia, 2020, v. 26, n. 1, p. e23, doi. 10.1111/hae.13896
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Novel treatment of combined factor V and factor VIII deficiency with Factor Eight Inhibitor Bypass Activity.
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- Haemophilia, 2020, v. 26, n. 1, p. e21, doi. 10.1111/hae.13895
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Prophylactic vs episodic treatment to prevent bleeds and preserve joint function in Thai children with moderate and severe haemophilia A.
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- Haemophilia, 2020, v. 26, n. 1, p. e18, doi. 10.1111/hae.13894
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Can we compare haemophilia carriers with clotting factor deficiency to male patients with mild haemophilia?
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- Haemophilia, 2020, v. 26, n. 1, p. 117, doi. 10.1111/hae.13891
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Bleeding assessment in haemophilia carriers—High rates of bleeding after surgical abortion and intrauterine device placement: A multicentre study in China.
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- Haemophilia, 2020, v. 26, n. 1, p. 122, doi. 10.1111/hae.13889
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Maternal and neonatal outcomes in carriers of haemophilia A and B: A Swedish Medical Birth Register study.
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- Haemophilia, 2020, v. 26, n. 1, p. e14, doi. 10.1111/hae.13884
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Safety and efficacy of turoctocog alfa in the prevention and treatment of bleeds in previously untreated paediatric patients with severe haemophilia A: Results from the guardian 4 multinational clinical trial.
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- Haemophilia, 2020, v. 26, n. 1, p. 64, doi. 10.1111/hae.13883
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Clinical application of Web Accessible Population Pharmacokinetic Service—Hemophilia (WAPPS‐Hemo): Patterns of blood sampling and patient characteristics among clinician users.
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- Haemophilia, 2020, v. 26, n. 1, p. 56, doi. 10.1111/hae.13882
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An international survey to inform priorities for new guidelines on von Willebrand disease.
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- Haemophilia, 2020, v. 26, n. 1, p. 106, doi. 10.1111/hae.13881
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Rhenium‐188 radiosynovectomy for chronic haemophilic synovitis: Evaluation of its safety and efficacy in haemophilic patients.
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- Haemophilia, 2020, v. 26, n. 1, p. 142, doi. 10.1111/hae.13880
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Chromic phosphate‐32 colloid radiosynovectomy for the treatment of haemophilic synovitis: A long‐term follow‐up study.
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- Haemophilia, 2020, v. 26, n. 1, p. 136, doi. 10.1111/hae.13879
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SHP656, a polysialylated recombinant factor VIII (PSA‐rFVIII): First‐in‐human study evaluating safety, tolerability and pharmacokinetics in patients with severe haemophilia A.
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- Haemophilia, 2020, v. 26, n. 1, p. 47, doi. 10.1111/hae.13878
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Emicizumab prophylaxis in patients with haemophilia A with and without inhibitors.
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- Haemophilia, 2020, v. 26, n. 1, p. 41, doi. 10.1111/hae.13877
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Fibrinogen concentrates in hereditary fibrinogen disorders: Past, present and future.
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- Haemophilia, 2020, v. 26, n. 1, p. 25, doi. 10.1111/hae.13876
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PEGylated biologics in haemophilia treatment: Current understanding of their long‐term safety.
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- Haemophilia, 2020, v. 26, n. 1, p. e11, doi. 10.1111/hae.13875
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Positive emotions despite substantial burden: The alchemy of haemophilia caregiving.
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- Haemophilia, 2020, v. 26, n. 1, p. 86, doi. 10.1111/hae.13874
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Sleeve gastrectomy in haemophilia type A: Reducing the costs of prophylaxis.
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- Haemophilia, 2020, v. 26, n. 1, p. e9, doi. 10.1111/hae.13872
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ST‐Segment Elevation Myocardial Infarction (STEMI) and Pulmonary Embolism in a Hemophilia A Patient Receiving Emicizumab and recombinant Activated Factor VII.
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- Haemophilia, 2020, v. 26, n. 1, p. e5, doi. 10.1111/hae.13871
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Characteristics and management of the haemophilia‐associated pseudotumours.
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- Haemophilia, 2020, v. 26, n. 1, p. 33, doi. 10.1111/hae.13870
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Patient profile, clinical characteristics and treatment response in acquired haemophilia A: A retrospective analysis of a single‐centre experience over a 3‐year period.
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- Haemophilia, 2020, v. 26, n. 1, p. e1, doi. 10.1111/hae.13869
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Achieving the unimaginable: Health equity in haemophilia.
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- Haemophilia, 2020, v. 26, n. 1, p. 17, doi. 10.1111/hae.13862
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Age‐related severity and distribution of haemophilic arthropathy of the knee, ankle and elbow among Chinese patients with haemophilia.
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- Haemophilia, 2020, v. 26, n. 1, p. 129, doi. 10.1111/hae.13858
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Issue Information.
- Published in:
- Haemophilia, 2020, v. 26, n. 1, p. 1, doi. 10.1111/hae.13788
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- Article
Instructions for Authors.
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- Haemophilia, 2020, v. 26, n. 1, p. 173, doi. 10.1111/hae.13787
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- Article