Works matching IS 13518216 AND DT 2021 AND VI 27
Results: 307
Cover Image.
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- Haemophilia, 2021, v. 27, n. 6, p. i, doi. 10.1111/hae.14463
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Haemostatic effect of adding tranexamic acid to emicizumab prophylaxis in severe haemophilia A: A preclinical study.
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- Haemophilia, 2021, v. 27, n. 6, p. 1002, doi. 10.1111/hae.14435
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Thrombomodulin in patients with mild to moderate bleeding tendency.
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- Haemophilia, 2021, v. 27, n. 6, p. 1028, doi. 10.1111/hae.14433
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Real‐world experience on the tolerability and safety of emicizumab prophylaxis in paediatric patients with severe haemophilia A with and without FVIII inhibitors.
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- Haemophilia, 2021, v. 27, n. 6, p. e698, doi. 10.1111/hae.14432
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Increased endoglin levels correlated with angiogenesis‐associated angiopoietin‐2 in haemophilia patients.
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- Haemophilia, 2021, v. 27, n. 6, p. e747, doi. 10.1111/hae.14430
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Clinical and patient reported outcome in total ankle replacement compared to ankle fusion in end‐stage haemophilic arthropathy.
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- Haemophilia, 2021, v. 27, n. 6, p. e739, doi. 10.1111/hae.14429
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Perceptions about the efficacy of extended half‐life (EHL) factor products in persons with haemophilia (PWH): A national survey of haemophilia providers from haemophilia treatment centres (HTCs) in the United States.
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- Haemophilia, 2021, v. 27, n. 6, p. e780, doi. 10.1111/hae.14427
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Haemophilia diagnostics with modern genomics.
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- Haemophilia, 2021, v. 27, n. 6, p. e754, doi. 10.1111/hae.14428
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Single centre, real‐world experience of perioperative rFIXFc use in adult patients with haemophilia B undergoing major and minor surgery.
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- Haemophilia, 2021, v. 27, n. 6, p. e690, doi. 10.1111/hae.14426
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Immune tolerance induction using Fc‐fusion‐protein recombinant factor IX in severe haemophilia B.
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- Haemophilia, 2021, v. 27, n. 6, p. e776, doi. 10.1111/hae.14424
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All‐cause mortality and causes of death in persons with haemophilia: A systematic review and meta‐analysis.
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- Haemophilia, 2021, v. 27, n. 6, p. 897, doi. 10.1111/hae.14423
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Monitoring of different factor VIII replacement products using a factor VIII one‐stage clotting assay on cobas t 511/711 analysers.
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- Haemophilia, 2021, v. 27, n. 6, p. e704, doi. 10.1111/hae.14416
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Surgery in mild haemophilia A patients with a history of inhibitor antibodies against factor VIII: Individualized management.
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- Haemophilia, 2021, v. 27, n. 6, p. e768, doi. 10.1111/hae.14415
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The actual and ideal roles of haemophilia treatment centre social workers in the United States and the barriers to ideal roles.
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- Haemophilia, 2021, v. 27, n. 6, p. e683, doi. 10.1111/hae.14414
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Descriptive analysis of bleeding symptoms in haemophilia carriers enrolled in the ATHNdataset.
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- Haemophilia, 2021, v. 27, n. 6, p. 1045, doi. 10.1111/hae.14422
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Patient preference for emicizumab versus prior factor therapy in people with haemophilia A: Results from the HAVEN 3 and HAVEN 4 studies.
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- Haemophilia, 2021, v. 27, n. 6, p. e772, doi. 10.1111/hae.14421
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Bleeding with iron deposition and vascular remodelling in subchondral cysts: A newly discovered feature unique to haemophilic arthropathy.
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- Haemophilia, 2021, v. 27, n. 6, p. e730, doi. 10.1111/hae.14417
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Delivery of AAV‐based gene therapy through haemophilia centres—A need for re‐evaluation of infrastructure and comprehensive care: A Joint publication of EAHAD and EHC.
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- Haemophilia, 2021, v. 27, n. 6, p. 967, doi. 10.1111/hae.14420
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The safety of activated eptacog beta in the management of bleeding episodes and perioperative haemostasis in adult and paediatric haemophilia patients with inhibitors.
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- Haemophilia, 2021, v. 27, n. 6, p. 921, doi. 10.1111/hae.14419
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PERSEPT 3: A phase 3 clinical trial to evaluate the haemostatic efficacy of eptacog beta (recombinant human FVIIa) in perioperative care in subjects with haemophilia A or B with inhibitors.
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- Haemophilia, 2021, v. 27, n. 6, p. 911, doi. 10.1111/hae.14418
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Prophylaxis in children with haemophilia in an evolving treatment landscape.
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- Haemophilia, 2021, v. 27, n. 6, p. 889, doi. 10.1111/hae.14412
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Haemophilic arthropathy: Contemporary management challenges and a future scenario.
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- Haemophilia, 2021, v. 27, n. 6, p. e765, doi. 10.1111/hae.14411
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Evaluation of the sexual health in people living with hemophilia.
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- Haemophilia, 2021, v. 27, n. 6, p. 993, doi. 10.1111/hae.14410
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Shortening the Haemophilia Activities List (HAL) from 42 items to 18 items.
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- Haemophilia, 2021, v. 27, n. 6, p. 1062, doi. 10.1111/hae.14408
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In response to WFH guidelines for the management of haemophilia, 3<sup>rd</sup> edition: Is there a difference between extended‐half‐life FVIII products or not?
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- Haemophilia, 2021, v. 27, n. 6, p. e762, doi. 10.1111/hae.14407
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Changes of static and dynamic spine alignment in patients with severe haemophilia.
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- Haemophilia, 2021, v. 27, n. 6, p. e721, doi. 10.1111/hae.14406
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Type 2N VWD: Conclusions from the Spanish PCM‐EVW‐ES project.
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- Haemophilia, 2021, v. 27, n. 6, p. 1007, doi. 10.1111/hae.14405
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Coordinating physiotherapy care for persons with haemophilia.
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- Haemophilia, 2021, v. 27, n. 6, p. 1051, doi. 10.1111/hae.14404
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Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States.
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- Haemophilia, 2021, v. 27, n. 6, p. 1037, doi. 10.1111/hae.14403
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Patient preferences for gene therapy in haemophilia: Results from the PAVING threshold technique survey.
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- Haemophilia, 2021, v. 27, n. 6, p. 957, doi. 10.1111/hae.14401
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The safety of plasma‐derived haemophilia factor concentrates – comments on "Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates" Nunes Valença I et al. (2021). Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates. Haemophilia. https://doi.org/10.1111/hae.14382
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- Haemophilia, 2021, v. 27, n. 6, p. e760, doi. 10.1111/hae.14400
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Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
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- Haemophilia, 2021, v. 27, n. 6, p. 1022, doi. 10.1111/hae.14399
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Low immunogenicity of emicizumab in persons with haemophilia A.
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- Haemophilia, 2021, v. 27, n. 6, p. 984, doi. 10.1111/hae.14398
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Diagnosis of von Willebrand disease: An assessment of the quality of testing in North American laboratories.
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- Haemophilia, 2021, v. 27, n. 6, p. e713, doi. 10.1111/hae.14397
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A qualitative study on the experiences of haemophilia carriers before, during and after pregnancy.
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- Haemophilia, 2021, v. 27, n. 6, p. e675, doi. 10.1111/hae.14396
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Single centre experience on Acquired Haemophilia A patients: Diagnosis, clinical management and analysis of factors predictive of response and outcome.
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- Haemophilia, 2021, v. 27, n. 6, p. e667, doi. 10.1111/hae.14395
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Pharmacokinetics of perioperative FVIII in adult patients with haemophilia A: An external validation and development of an alternative population pharmacokinetic model.
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- Haemophilia, 2021, v. 27, n. 6, p. 974, doi. 10.1111/hae.14393
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Effect of lower VWF and FXI levels on levonorgestrel IUS and endometrial ablation treatment success in heavy menstrual bleeding: An exploratory study.
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- Haemophilia, 2021, v. 27, n. 6, p. e756, doi. 10.1111/hae.14392
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Persistence of haemostatic response following gene therapy with valoctocogene roxaparvovec in severe haemophilia A.
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- Haemophilia, 2021, v. 27, n. 6, p. 947, doi. 10.1111/hae.14391
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Prostate interventions in patients with mild haemophilia: Safe and feasible.
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- Haemophilia, 2021, v. 27, n. 6, p. e659, doi. 10.1111/hae.14388
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Immune tolerance induction in severe haemophilia A: A UKHCDO inhibitor and paediatric working party consensus update.
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- Haemophilia, 2021, v. 27, n. 6, p. 932, doi. 10.1111/hae.14381
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Clinical attributes and treatment characteristics are associated with work productivity and activity impairment in people with severe haemophilia A.
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- Haemophilia, 2021, v. 27, n. 6, p. 938, doi. 10.1111/hae.14302
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Issue Information.
- Published in:
- Haemophilia, 2021, v. 27, n. 6, p. i, doi. 10.1111/hae.14058
- Publication type:
- Article
Identification of F8 rearrangements in carrier and non‐carrier mothers of haemophilia A patients.
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- Haemophilia, 2021, v. 27, n. 5, p. e654, doi. 10.1111/hae.14394
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Quality of periprocedural care in patients with von Willebrand disease.
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- Haemophilia, 2021, v. 27, n. 5, p. 830, doi. 10.1111/hae.14389
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Quality of life of people with hereditary factor XIII deficiency treated at a reference centre.
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- Haemophilia, 2021, v. 27, n. 5, p. e649, doi. 10.1111/hae.14387
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Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment.
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- Haemophilia, 2021, v. 27, n. 5, p. 769, doi. 10.1111/hae.14383
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Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates.
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- Haemophilia, 2021, v. 27, n. 5, p. e645, doi. 10.1111/hae.14382
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Changes in pain profile of patients with haemophilia during 1‐year follow‐up.
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- Haemophilia, 2021, v. 27, n. 5, p. 783, doi. 10.1111/hae.14380
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European principles of care for women and girls with inherited bleeding disorders.
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- Haemophilia, 2021, v. 27, n. 5, p. 837, doi. 10.1111/hae.14379
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