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FIXing postinfusion monitoring: Assay experiences with N9‐GP (nonacog beta pegol; Refixia<sup>®</sup>; Rebinyn<sup>®</sup>).
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 154, doi. 10.1111/hae.13671
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- Publication type:
- Article
The invisible child: Sibling experiences of growing up with a brother with severe haemophilia—An interpretative phenomenological analysis.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 84, doi. 10.1111/hae.13659
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- Publication type:
- Article
Mycophenolate mofetil as adjunctive therapy in acquired haemophilia A.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Accurate measurement of extended half‐life and unmodified factor VIII low levels with one‐stage FVIII assays is dependent on the matrix of calibration curves.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. e19, doi. 10.1111/hae.13656
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- Publication type:
- Article
A rare presentation of homozygous factor X deficiency in a pregnant patient: A case report and review of the literature.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
A single‐centre study of management of pregnant women with von Willebrand disease.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 127, doi. 10.1111/hae.13638
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- Publication type:
- Article
Posturographic and ankle muscle activation characteristics in patients with haemophilia.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 136, doi. 10.1111/hae.13650
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- Publication type:
- Article
Measurement of joint health in persons with haemophilia: A systematic review of the measurement properties of haemophilia‐specific instruments.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. e1, doi. 10.1111/hae.13631
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- Publication type:
- Article
A case of moderate haemophilia A with inhibitor, carrying the p.R1800H mutation, complicated with juvenile idiopathic arthritis.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Over two decades of orthopaedic surgery in patients with inhibitors—Quantifying the complication of bleeding.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 21, doi. 10.1111/hae.13647
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- Publication type:
- Article
Potential limits of AAV‐based gene therapy with the use of new transgenes expressing factor IX fusion proteins.
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- Haemophilia, 2019, v. 25, n. 1, p. e11, doi. 10.1111/hae.13651
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- Publication type:
- Article
The prevalence and burden of hand and wrist bleeds in von Willebrand disease.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Test‐retest properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire and its constituent domains.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 75, doi. 10.1111/hae.13649
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- Publication type:
- Article
Does haemophilia slow down the development of liver fibrosis?
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
A novel approach to immune tolerance induction in haemophilia A with factor VIII inhibitor.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Samuel Armstrong Lane's first successful treatment of haemophilia with blood transfusion in 1840: Could this also be the first successful bypassing therapy?
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Analytical variation in factor VIII one‐stage and chromogenic assays: Experiences from the ECAT external quality assessment programme.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 162, doi. 10.1111/hae.13643
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- Publication type:
- Article
Cardiovascular disease‐related hospitalization and mortality among persons with von Willebrand disease: A nationwide register study in Sweden.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 109, doi. 10.1111/hae.13642
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- Publication type:
- Article
Emicizumab: Review of the literature and critical appraisal.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 11, doi. 10.1111/hae.13641
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- Publication type:
- Article
Intravenous immunoglobulin in patients with acquired Von Willebrand syndrome: A single referral centre experience.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Thromboelastometry profiles after "in vitro" addition of a new plasma‐derived factor V concentrate to whole blood from parahaemophilia patients.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Utility valuation of health states for haemophilia and related complications in Europe and in the United States.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 92, doi. 10.1111/hae.13634
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- Publication type:
- Article
Recommendations for the clinical interpretation of genetic variants and presentation of results to patients with inherited bleeding disorders. A UK Haemophilia Centre Doctors' Organisation Good Practice Paper.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 116, doi. 10.1111/hae.13637
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- Publication type:
- Article
Joint status in Spanish haemophilia B patients assessed using the Haemophilia Early Arthropathy Detection with Ultrasound (HEAD‐US) score.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 144, doi. 10.1111/hae.13628
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- Publication type:
- Article
Prevalence of FVIII inhibitors in severe haemophilia A patients: Effect of treatment and genetic factors in an Indian population.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 67, doi. 10.1111/hae.13633
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- Publication type:
- Article
Issue Information.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 5, doi. 10.1111/hae.13572
- Publication type:
- Article
Sports participation and physical activity in patients with von Willebrand disease.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 101, doi. 10.1111/hae.13629
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- Publication type:
- Article
Concizumab restores thrombin generation potential in patients with haemophilia: Pharmacokinetic/pharmacodynamic modelling results of concizumab phase 1/1b data.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 60, doi. 10.1111/hae.13627
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- Publication type:
- Article
Severe acquired von Willebrand syndrome secondary to systemic lupus erythematosus.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Continuous infusion of simoctocog alfa in haemophilia A patients undergoing surgeries.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 54, doi. 10.1111/hae.13625
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- Publication type:
- Article
Health‐related quality of life in paediatric haemophilia B patients treated with rIX‐FP.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 45, doi. 10.1111/hae.13624
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- Publication type:
- Article
Assessment of tensile mechanical properties of the Achilles tendon in adult patients with haemophilic arthropathy. Reproducibility study.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
The effect of emicizumab prophylaxis on health‐related outcomes in persons with haemophilia A with inhibitors: HAVEN 1 Study.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 33, doi. 10.1111/hae.13618
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- Publication type:
- Article
Instructions for Authors.
- Published in:
- Haemophilia, 2019, v. 25, n. 1, p. 170, doi. 10.1111/hae.13571
- Publication type:
- Article