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Editorial Board.
- Published in:
- Haemophilia, 2016, v. 22, n. 6, p. 815, doi. 10.1111/hae.12827
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- Article
Table of Contents.
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- Haemophilia, 2016, v. 22, n. 6, p. 817, doi. 10.1111/hae.12828
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- Article
Instructions for Authors.
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- Haemophilia, 2016, v. 22, n. 6, p. 966, doi. 10.1111/hae.12829
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- Article
Feasibility of video consultations in case of acute complications in children with haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. e567, doi. 10.1111/hae.13109
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TRUST trial: BAY 86-6150 use in haemophilia with inhibitors and assessment for immunogenicity.
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- Haemophilia, 2016, v. 22, n. 6, p. 873, doi. 10.1111/hae.12994
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Lower doses of recombinant porcine factor VIII maintain excellent haemostatic efficacy.
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- Haemophilia, 2016, v. 22, n. 6, p. e549, doi. 10.1111/hae.13038
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Usefulness of the Total Thrombus-Formation Analysis System (T- TAS) in the diagnosis and characterization of von Willebrand disease.
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- Haemophilia, 2016, v. 22, n. 6, p. 949, doi. 10.1111/hae.12971
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- Article
Changes in health-related quality of life with treatment of longer-acting clotting factors: results in the A- LONG and B- LONG clinical studies.
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- Haemophilia, 2016, v. 22, n. 6, p. 866, doi. 10.1111/hae.12987
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Long-term effects of joint bleeding before starting prophylaxis in severe haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. 852, doi. 10.1111/hae.12959
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- Article
Long-term outcome of haemophilia A patients after successful immune tolerance induction therapy using a single plasma-derived FVIII/VWF product: the long-term ITI study.
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- Haemophilia, 2016, v. 22, n. 6, p. 859, doi. 10.1111/hae.12986
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- Article
Analyses of joint health and influencing factors in different age groups of Chinese children with haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. e545, doi. 10.1111/hae.12983
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Optimization of home treatment in haemophilia: effects of transmural support by a haemophilia nurse on adherence and quality of life.
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- Haemophilia, 2016, v. 22, n. 6, p. 841, doi. 10.1111/hae.13043
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Evaluation of the utility of the ISTH- BAT in haemophilia carriers: a multinational study.
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- Haemophilia, 2016, v. 22, n. 6, p. 912, doi. 10.1111/hae.13089
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Acquired autoimmune thrombotic thrombocytopenic purpura in a case of severe haemophilia A.
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- Haemophilia, 2016, v. 22, n. 6, p. e565, doi. 10.1111/hae.13091
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- Article
Functional outcome of total knee arthroplasty in patients with haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. 919, doi. 10.1111/hae.12999
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- Article
A world-wide survey and field study in clinical haemostasis laboratories to evaluate FVIII:C activity assay variability of ADYNOVATE and OBIZUR in comparison with ADVATE.
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- Haemophilia, 2016, v. 22, n. 6, p. 957, doi. 10.1111/hae.13001
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Prenatal diagnosis for haemophilia: the Thai experience.
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- Haemophilia, 2016, v. 22, n. 6, p. 880, doi. 10.1111/hae.13002
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Pain sensitivity in patients with haemophilia following moderate aerobic exercise intervention.
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- Haemophilia, 2016, v. 22, n. 6, p. 886, doi. 10.1111/hae.13016
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Long-term liver-related morbidity and mortality related to chronic hepatitis C virus infection in Swedish patients with inherited bleeding disorders.
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- Haemophilia, 2016, v. 22, n. 6, p. e494, doi. 10.1111/hae.13020
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- Article
SPINART study: validation of the extended magnetic resonance imaging scale for evaluation of joint status in adult patients with severe haemophilia A using baseline data.
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- Haemophilia, 2016, v. 22, n. 6, p. e519, doi. 10.1111/hae.13022
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- Article
Correlating clinical and radiological assessment of joints in haemophilia: results of a cross sectional study.
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- Haemophilia, 2016, v. 22, n. 6, p. 925, doi. 10.1111/hae.13023
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A single-centre study of haemostatic outcomes of joint replacement in von Willebrand disease and control patients and an analysis of the literature.
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- Haemophilia, 2016, v. 22, n. 6, p. 934, doi. 10.1111/hae.13027
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Validity of the Portuguese CHO-KLAT in Brazil.
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- Haemophilia, 2016, v. 22, n. 6, p. 894, doi. 10.1111/hae.13031
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A bodyweight-dependent allometric exponent model for scaling clearance of clotting factor VIII and IX from infants to adults.
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- Haemophilia, 2016, v. 22, n. 6, p. e570, doi. 10.1111/hae.13116
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Relationship between physical function and biomechanical gait patterns in boys with haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. e512, doi. 10.1111/hae.13118
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Connective tissue growth factor ( CTGF/ CCN2) in haemophilic arthropathy and arthrofibrosis: a histological analysis.
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- Haemophilia, 2016, v. 22, n. 6, p. e527, doi. 10.1111/hae.13049
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus.
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- Haemophilia, 2016, v. 22, n. 6, p. 898, doi. 10.1111/hae.13061
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Extended half-life factor VIII for immune tolerance induction in haemophilia.
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- Haemophilia, 2016, v. 22, n. 6, p. e552, doi. 10.1111/hae.13064
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Recognizing the need for personalization of haemophilia patient-reported outcomes in the prophylaxis era.
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- Haemophilia, 2016, v. 22, n. 6, p. 825, doi. 10.1111/hae.13066
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Obstetric bleeding among women with inherited bleeding disorders: a retrospective study.
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- Haemophilia, 2016, v. 22, n. 6, p. 906, doi. 10.1111/hae.13067
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Stop only advising physical activity in adults with haemophilia... prescribe it now! The role of exercise therapy and nutrition in chronic musculoskeletal diseases.
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- Haemophilia, 2016, v. 22, n. 6, p. e554, doi. 10.1111/hae.13073
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Expression and release of platelet protein disulphide isomerase in patients with haemophilia A.
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- Haemophilia, 2016, v. 22, n. 6, p. e537, doi. 10.1111/hae.13074
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Evidence for and cost-effectiveness of physiotherapy in haemophilia: a Dutch perspective.
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- Haemophilia, 2016, v. 22, n. 6, p. 943, doi. 10.1111/hae.13076
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Long-term remission of acquired von Willebrand syndrome associated with multiple myeloma using bortezomib and dexamethasone therapy.
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- Haemophilia, 2016, v. 22, n. 6, p. e557, doi. 10.1111/hae.13077
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Moderate X-chromosome inactivation skewing underlies factor VIII activity in symptomatic carriers from a family with mild haemophilia A.
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- Haemophilia, 2016, v. 22, n. 6, p. e559, doi. 10.1111/hae.13083
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von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
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- Haemophilia, 2016, v. 22, n. 6, p. e502, doi. 10.1111/hae.13084
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A prospective study of von Willebrand factor levels and bleeding in pregnant women with type 1 von Willebrand disease.
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- Haemophilia, 2016, v. 22, n. 6, p. e562, doi. 10.1111/hae.13086
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The association of haemophilic arthropathy with Health-Related Quality of Life: a post hoc analysis.
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- Haemophilia, 2016, v. 22, n. 6, p. 833, doi. 10.1111/hae.13120
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Chemical vs. radioactive synoviorthesis for treatment of chronic haemophilic synovitis: Syrian experience.
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- Haemophilia, 2016, v. 22, n. 6, p. e573, doi. 10.1111/hae.13129
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- Article
Editorial Board.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 635, doi. 10.1111/hae.12824
- Publication type:
- Article
Table of Contents.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 637, doi. 10.1111/hae.12825
- Publication type:
- Article
Instructions for Authors.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 814, doi. 10.1111/hae.12826
- Publication type:
- Article
Identification of mutations in the F8 and F9 gene in families with haemophilia using targeted high-throughput sequencing.
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- Haemophilia, 2016, v. 22, n. 5, p. e427, doi. 10.1111/hae.12924
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- Publication type:
- Article
Potential biomarkers of haemophilic arthropathy: correlations with compatible additive magnetic resonance imaging scores.
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- Haemophilia, 2016, v. 22, n. 5, p. 760, doi. 10.1111/hae.12936
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Prospective evaluation of treatment regimens, efficacy and safety of a recombinant factor VIII concentrate in haemophilia A: the German EffeKt study.
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- Haemophilia, 2016, v. 22, n. 5, p. 684, doi. 10.1111/hae.12941
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- Article
Optimization of the thrombin generation test components to measure potency of factor VIII concentrates.
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- Haemophilia, 2016, v. 22, n. 5, p. 780, doi. 10.1111/hae.12943
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- Article
Daclatasvir/peginterferon lambda-1a/ribavirin in patients with chronic HCV infection and haemophilia who are treatment naïve or prior relapsers to peginterferon alfa-2a/ribavirin.
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- Haemophilia, 2016, v. 22, n. 5, p. 692, doi. 10.1111/hae.12947
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Assessment and validation of a defined fluid restriction protocol in the use of subcutaneous desmopressin for children with inherited bleeding disorders.
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- Haemophilia, 2016, v. 22, n. 5, p. 700, doi. 10.1111/hae.12949
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- Article
Haemarthrosis model in mice: BSS - Bleeding Severity Score assessment system.
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- Haemophilia, 2016, v. 22, n. 5, p. 790, doi. 10.1111/hae.12950
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- Article
Efficacy and safety of BAY 81-8973, a full-length recombinant factor VIII: results from the LEOPOLD I trial.
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- Haemophilia, 2016, v. 22, n. 5, p. 706, doi. 10.1111/hae.12952
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- Article