Found: 48
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Diagnostic delay in acquired haemophilia: Analysis of causes and consequences in a 20‐year Spanish cohort.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
The multiple benefits of sport in haemophilia.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 341, doi. 10.1111/hae.13496
- By:
- Publication type:
- Article
The interaction of factor V and tissue factor pathway inhibitor in a myeloma patient with acquired factor V deficiency.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 344, doi. 10.1111/hae.13495
- By:
- Publication type:
- Article
Moderate and severe haemophilia in Spain: An epidemiological update.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Frequencies of intron 1 and 22 inversions of factor VIII gene: A first report in Afghan patients with severe haemophilia A.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Cost‐utility of a six‐month programmed sports therapy (PST) in patients with haemophilia.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 385, doi. 10.1111/hae.13459
- By:
- Publication type:
- Article
Pharmacokinetic modelling and validation of the half‐life extension needed to reduce the burden of infusions compared with standard factor VIII.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 376, doi. 10.1111/hae.13483
- By:
- Publication type:
- Article
Assessment of passive musculoarticular ankle stiffness in children, adolescents and young adults with haemophilic ankle arthropathy.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. e103, doi. 10.1111/hae.13467
- By:
- Publication type:
- Article
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Inheritance of von Willebrand disease Vicenza in a Japanese family.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Replacement therapy during surgery in von Willebrand disease needs personalization.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 338, doi. 10.1111/hae.13488
- By:
- Publication type:
- Article
DDAVP trial in discrepant non‐severe haemophilia A patients.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Real life experiences of a PK dosing study—Challenges and lessons learned.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Management of pregnancy complications in type 2N von Willebrand disease associated to a novel mutation.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Successful multi‐modal immune tolerance induction for factor IX deficiency with inhibitors and allergic reactions.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Screening of haemophilia carriers in moderate and severe haemophilia A and B: Prevalence and determinants.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Successful treatment of acquired von Willebrand disease with lenalidomide leading to dramatic resolution of intractable gastrointestinal bleeding: A case report.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Response: The coagulation laboratory monitoring of AFSTYLA single‐chain FVIII concentrate.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Management of haemophilia carriers around the time of their delivery: Phenotypic variation requiring customization of management.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Principles of haemophilia care: The Asia‐Pacific perspective.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 366, doi. 10.1111/hae.13425
- By:
- Publication type:
- Article
Retracted: National home infusion teaching guidelines will improve quality of care and patient outcomes in haemophilia treatment centres across the USA.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Analysis of current perioperative management with Haemate<sup>®</sup> P/Humate P<sup>®</sup> in von Willebrand disease: Identifying the need for personalized treatment.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 460, doi. 10.1111/hae.13451
- By:
- Publication type:
- Article
Evaluation of chromogenic factor IX assays by automated protocols.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 492, doi. 10.1111/hae.13446
- By:
- Publication type:
- Article
Long‐term clinical and economic outcomes in previously untreated paediatric patients with severe haemophilia A: A nationwide real‐world study with 700 person‐years.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 436, doi. 10.1111/hae.13447
- By:
- Publication type:
- Article
Effectiveness of the Medtep Hemophilia online platform for adherence to prophylactic treatment in haemophilia patients: Results from a 1‐year observational study.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 452, doi. 10.1111/hae.13444
- By:
- Publication type:
- Article
A rare case of late development of inhibitor in haemophilia B with a complex course, and review of the literature.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Movement behaviour in adults with haemophilia compared to healthy adults.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 445, doi. 10.1111/hae.13441
- By:
- Publication type:
- Article
Advantage of recombinant von Willebrand factor for peri‐operative management in paediatric acquired von Willebrand syndrome.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Physiotherapist inter‐rater reliability of the Haemophilia Early Arthropathy Detection with Ultrasound protocol.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 471, doi. 10.1111/hae.13440
- By:
- Publication type:
- Article
Use of ultrasound for evaluation of painful joint episodes perceived as haemarthrosis in adult patients with severe haemophilia.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Defining extended half‐life rFVIII—A critical review of the evidence.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 348, doi. 10.1111/hae.13438
- By:
- Publication type:
- Article
The importance of ABO blood group in pharmacokinetic studies in haemophilia A.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Effects of pre‐analytical heat treatment in factor VIII (FVIII) inhibitor assays on FVIII antibody levels.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 487, doi. 10.1111/hae.13435
- By:
- Publication type:
- Article
Reagent substitutions in the Centers for Disease Control and Prevention Nijmegen‐Bethesda assay for factor VIII inhibitors.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Arteriovenous shunts as venous access in children with haemophilia.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 429, doi. 10.1111/hae.13433
- By:
- Publication type:
- Article
Clinical use of recombinant factor VIII Fc and recombinant factor IX Fc in patients with haemophilia A and B.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 414, doi. 10.1111/hae.13432
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- Publication type:
- Article
World bleeding disorders registry: The pilot study.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
In vitro characterization of MOD‐5014, a novel long‐acting carboxy‐terminal peptide (CTP)‐modified activated FVII.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 477, doi. 10.1111/hae.13428
- By:
- Publication type:
- Article
High proportion of patients with bleeding of unknown cause in persons with a mild‐to‐moderate bleeding tendency: Results from the Vienna Bleeding Biobank (VIBB).
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 405, doi. 10.1111/hae.13422
- By:
- Publication type:
- Article
Clinical trials and registries in haemophilia: Opponents or collaborators? Comparison of PUP data derived from different data sources.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 420, doi. 10.1111/hae.13421
- By:
- Publication type:
- Article
Male gender, school attendance and sports participation are positively associated with health‐related quality of life in children and adolescents with congenital bleeding disorders.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 395, doi. 10.1111/hae.13420
- By:
- Publication type:
- Article
Ligneous cervicitis and endometritis: A gynaecological presentation of congenital plasminogen deficiency.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 359, doi. 10.1111/hae.13418
- By:
- Publication type:
- Article
Point‐of‐care ultrasonography in haemophilia care: Training and competency for muscular haematomas.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 335, doi. 10.1111/hae.13417
- By:
- Publication type:
- Article
Burden of illness and costs among paediatric haemophilia patients with and without central venous access devices treated in US hospitals.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. e93, doi. 10.1111/hae.13404
- By:
- Publication type:
- Article
Real‐world experience with use of Antihemophilic Factor (Recombinant), PEGylated for prophylaxis in severe haemophilia A.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. e84, doi. 10.1111/hae.13403
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 329, doi. 10.1111/hae.13337
- Publication type:
- Article
Instructions for Authors.
- Published in:
- Haemophilia, 2018, v. 24, n. 3, p. 504, doi. 10.1111/hae.13336
- Publication type:
- Article