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Parental perspectives on gene therapy for children with haemophilia: The Exigency study.
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- Haemophilia, 2021, v. 27, n. 1, p. 120, doi. 10.1111/hae.14188
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Impact of humanitarian aid linked prophylaxis in Côte d'Ivoire (Ivory Coast).
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- Haemophilia, 2021, v. 27, n. 1, p. 9, doi. 10.1111/hae.14246
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Comparison of bypassing agents in patients on emicizumab using global hemostasis assays.
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- Haemophilia, 2021, v. 27, n. 1, p. 164, doi. 10.1111/hae.14213
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Management of people with haemophilia A undergoing surgery while receiving emicizumab prophylaxis: Real‐world experience from a large comprehensive treatment centre in the US.
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- Haemophilia, 2021, v. 27, n. 1, p. 90, doi. 10.1111/hae.14212
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Evaluation of anti‐factor VIII antibody levels in patients with haemophilia A receiving immune tolerance induction therapy or bypassing agents.
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- Haemophilia, 2021, v. 27, n. 1, p. e40, doi. 10.1111/hae.14202
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Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature.
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- Haemophilia, 2021, v. 27, n. 1, p. 26, doi. 10.1111/hae.14211
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Assessing the test–retest reliability and smallest detectable change of the Haemophilia Activities List.
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- Haemophilia, 2021, v. 27, n. 1, p. 108, doi. 10.1111/hae.14226
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Safety and efficacy of percutaneous radiofrequency ablation for hepatocellular carcinoma patients with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. 100, doi. 10.1111/hae.14220
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Reimbursing the value of gene therapy care in an era of uncertainty.
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- Haemophilia, 2021, v. 27, n. 1, p. 12, doi. 10.1111/hae.14218
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An overview of patients with haemophilia A in China: Epidemiology, disease severity and treatment strategies.
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- Haemophilia, 2021, v. 27, n. 1, p. e51, doi. 10.1111/hae.14217
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Feasibility and outcomes of low‐dose and low‐frequency prophylaxis with recombinant extended half‐life products (Fc‐rFVIII and Fc‐rFIX) in Ivorian children with hemophilia: Two‐year experience in the setting of World Federation of Haemophilia humanitarian aid programme
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- Haemophilia, 2021, v. 27, n. 1, p. 33, doi. 10.1111/hae.14216
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Safety and efficacy of nonacog alfa for the treatment of haemophilia B in children younger than 6 years of age in a routine clinical care setting: the EUREKIX registry study.
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- Haemophilia, 2021, v. 27, n. 1, p. e60, doi. 10.1111/hae.14215
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Biomarkers and immunological parameters in haemophilia and rheumatoid arthritis patients: a comparative multiplexing laboratory study.
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- Haemophilia, 2021, v. 27, n. 1, p. e119, doi. 10.1111/hae.14200
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Detection and evaluation of haemophilic arthropathy: Which tools may be considered more reliable.
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- Haemophilia, 2021, v. 27, n. 1, p. 156, doi. 10.1111/hae.14153
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Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China.
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- Haemophilia, 2021, v. 27, n. 1, p. e88, doi. 10.1111/hae.14206
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Patient perspectives regarding gene therapy in haemophilia: Interviews from the PAVING study.
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- Haemophilia, 2021, v. 27, n. 1, p. 129, doi. 10.1111/hae.14190
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Long‐term safety and efficacy of emicizumab for up to 5.8 years and patients' perceptions of symptoms and daily life: A phase 1/2 study in patients with severe haemophilia A.
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- Haemophilia, 2021, v. 27, n. 1, p. 81, doi. 10.1111/hae.14205
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How we diagnose 2M von Willebrand disease (VWD): Use of a strategic algorithmic approach to distinguish 2M VWD from other VWD types.
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- Haemophilia, 2021, v. 27, n. 1, p. 137, doi. 10.1111/hae.14204
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Diagnosis of von Willebrand disease in Western Mexico.
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- Haemophilia, 2021, v. 27, n. 1, p. e78, doi. 10.1111/hae.14203
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The effectiveness of manual therapy in addition to passive stretching exercises in the treatment of patients with haemophilic knee arthropathy: A randomized, single‐blind clinical trial.
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- Haemophilia, 2021, v. 27, n. 1, p. e110, doi. 10.1111/hae.14181
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Disease burden and remaining unmet need in patients with haemophilia A treated with primary prophylaxis.
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- Haemophilia, 2021, v. 27, n. 1, p. 113, doi. 10.1111/hae.14171
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Characterisation of healthcare utilisation and cost of haemophilia care in real‐life: A 4‐year follow‐up study in Finland.
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- Haemophilia, 2021, v. 27, n. 1, p. e30, doi. 10.1111/hae.14197
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Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes.
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- Haemophilia, 2021, v. 27, n. 1, p. e69, doi. 10.1111/hae.14195
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Real‐world evidence on health resource use among patients with haemophilia and inhibitor exhibiting severe bleeding episodes.
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- Haemophilia, 2021, v. 27, n. 1, p. 69, doi. 10.1111/hae.14194
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Real‐world data of immune tolerance induction using recombinant factor VIII Fc fusion protein in patients with severe haemophilia A with inhibitors at high risk for immune tolerance induction failure: A follow‐up retrospective analysis.
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- Haemophilia, 2021, v. 27, n. 1, p. 19, doi. 10.1111/hae.14192
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Management of COVID‐19‐associated coagulopathy in persons with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. 41, doi. 10.1111/hae.14191
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Feasibility, safety and muscle activity during flywheel vs traditional strength training in adult patients with severe haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. e102, doi. 10.1111/hae.14170
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Joint replacement for the management of haemophilic arthropathy in patients with inhibitors: A long‐term experience at a single Haemophilia centre.
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- Haemophilia, 2021, v. 27, n. 1, p. e93, doi. 10.1111/hae.14169
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Validation of a new instrument to measure disease‐related distress among patients with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. 60, doi. 10.1111/hae.14187
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Modelling future usage and cost of factor and emicizumab to treat haemophilia A for the US Western States Region IX haemophilia treatment centres.
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- Haemophilia, 2021, v. 27, n. 1, p. e22, doi. 10.1111/hae.14159
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Natural history study of factor IX deficiency with focus on treatment and complications (B‐Natural).
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- Haemophilia, 2021, v. 27, n. 1, p. 49, doi. 10.1111/hae.14139
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Cost‐utility analysis of emicizumab prophylaxis in haemophilia A patients with factor VIII inhibitors in Korea.
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- Haemophilia, 2021, v. 27, n. 1, p. e12, doi. 10.1111/hae.14143
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Cost‐effectiveness of emicizumab vs bypassing agents in the prevention of bleeding episodes in haemophilia A patients with anti‐FVIII inhibitors in France.
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- Haemophilia, 2021, v. 27, n. 1, p. e1, doi. 10.1111/hae.14129
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Daratumumab rapidly reduces high‐titre factor VIII inhibitors in haemophilia A patients during life‐threatening haemorrhages.
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- Haemophilia, 2021, v. 27, n. 1, p. e155, doi. 10.1111/hae.14118
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Assessment of sexuality information needs in haemophilia: Evaluation of a multi‐ethnic patient cohort.
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- Haemophilia, 2021, v. 27, n. 1, p. e160, doi. 10.1111/hae.14121
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Intelligent game engines for home exercises (exergames) in boys with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. e151, doi. 10.1111/hae.14116
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Recombinant porcine factor VIII use in bleed treatment in non‐severe haemophilia A inhibitor patients: Dosing strategies and efficacy.
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- Haemophilia, 2021, v. 27, n. 1, p. e147, doi. 10.1111/hae.14111
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Safety and blood loss in spinal surgery for haemophiliacs: Case series of Japanese haemophiliacs.
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- Haemophilia, 2021, v. 27, n. 1, p. e143, doi. 10.1111/hae.14103
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Severe bleeding in a patient with factor XIII deficiency and COVID‐19.
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- Haemophilia, 2021, v. 27, n. 1, p. e140, doi. 10.1111/hae.14088
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COVID‐19 and telemedicine in haemophilia in a patient with severe haemophilia A and orthopaedic surgery.
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- Haemophilia, 2021, v. 27, n. 1, p. e137, doi. 10.1111/hae.14087
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Thrombin generation assay modifications needed for its application to monitoring of replacement therapy for haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. e129, doi. 10.1111/hae.14024
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The diagnosis of a haemophilia A carrier over 2 decades.
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- Haemophilia, 2021, v. 27, n. 1, p. e133, doi. 10.1111/hae.14073
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Issue Information.
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- Haemophilia, 2021, v. 27, n. 1, p. 1, doi. 10.1111/hae.14058
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- Article
Biomarkers of bone disease in persons with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. 149, doi. 10.1111/hae.13986
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Factor VII and factor X deficiency in a child with a chromosome 13q duplication and deletion.
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- Haemophilia, 2021, v. 27, n. 1, p. e127, doi. 10.1111/hae.13065
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