Works matching IS 13518216 AND DT 2016 AND VI 22 AND IP 5
Results: 57
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.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e427, doi. 10.1111/hae.12924
- By:
- Publication type:
- Article
Potential biomarkers of haemophilic arthropathy: correlations with compatible additive magnetic resonance imaging scores.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 760, doi. 10.1111/hae.12936
- By:
- Publication type:
- Article
Editorial Board.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 635, doi. 10.1111/hae.12824
- Publication type:
- Article
Prospective evaluation of treatment regimens, efficacy and safety of a recombinant factor VIII concentrate in haemophilia A: the German EffeKt study.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 684, doi. 10.1111/hae.12941
- By:
- Publication type:
- Article
Optimization of the thrombin generation test components to measure potency of factor VIII concentrates.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 780, doi. 10.1111/hae.12943
- By:
- Publication type:
- 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.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 692, doi. 10.1111/hae.12947
- By:
- Publication type:
- Article
Assessment and validation of a defined fluid restriction protocol in the use of subcutaneous desmopressin for children with inherited bleeding disorders.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 700, doi. 10.1111/hae.12949
- By:
- Publication type:
- Article
Haemarthrosis model in mice: BSS - Bleeding Severity Score assessment system.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 790, doi. 10.1111/hae.12950
- By:
- Publication type:
- Article
Efficacy and safety of BAY 81-8973, a full-length recombinant factor VIII: results from the LEOPOLD I trial.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 706, doi. 10.1111/hae.12952
- By:
- Publication type:
- Article
Experience of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency undergoing surgery.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 713, doi. 10.1111/hae.12954
- By:
- Publication type:
- Article
Practical aspects of factor concentrate use in patients with von Willebrand disease undergoing invasive procedures: a European survey.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 739, doi. 10.1111/hae.12955
- By:
- Publication type:
- Article
Circulating FVIII-specific IgG, IgA and IgM memory B cells from haemophilia A patients.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 799, doi. 10.1111/hae.12958
- By:
- Publication type:
- Article
Can the phenotype of inherited fibrinogen disorders be predicted?
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 667, doi. 10.1111/hae.12967
- By:
- Publication type:
- Article
Lupus anticoagulants associated inhibitor against factor IX in a young patient with haemophilia B.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e437, doi. 10.1111/hae.12956
- By:
- Publication type:
- Article
Inhibitor development in previously untreated patients with severe haemophilia A: a nationwide multicentre study in Finland.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 721, doi. 10.1111/hae.12974
- By:
- Publication type:
- Article
Population pharmacokinetic modelling of factor IX activity after administration of recombinant factor IX in patients with haemophilia B.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e359, doi. 10.1111/hae.12969
- By:
- Publication type:
- Article
The evolution of comprehensive haemophilia care in the United States: perspectives from the frontline.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 676, doi. 10.1111/hae.12970
- By:
- Publication type:
- Article
RCT of a 6-month programmed sports therapy ( PST) in patients with haemophilia - Improvement of physical fitness.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 765, doi. 10.1111/hae.12957
- By:
- Publication type:
- Article
Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 752, doi. 10.1111/hae.12978
- By:
- Publication type:
- Article
Genotyping might help therapeutic decision-making in patients with von Willebrand disease type 2 B.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e439, doi. 10.1111/hae.12960
- By:
- Publication type:
- Article
Factor VIII assay variability in postinfusion samples containing full length and B-domain deleted FVIII.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 806, doi. 10.1111/hae.12962
- By:
- Publication type:
- Article
Comparative pharmacokinetics of rVIII-SingleChain and octocog alfa (Advate<sup>®</sup>) in patients with severe haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 730, doi. 10.1111/hae.12985
- By:
- Publication type:
- Article
First trimester prenatal diagnosis of severe FXIII deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e443, doi. 10.1111/hae.12982
- By:
- Publication type:
- Article
Interim results from a large multinational extension trial (guardian<sup>™</sup>2) using turoctocog alfa for prophylaxis and treatment of bleeding in patients with severe haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e445, doi. 10.1111/hae.12990
- By:
- Publication type:
- Article
Acquired haemophilia A in a Jehovah's Witness.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e449, doi. 10.1111/hae.12992
- By:
- Publication type:
- Article
Adherence to prophylactic treatment in patients with haemophilia in Germany.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e367, doi. 10.1111/hae.13003
- By:
- Publication type:
- Article
Total joint replacement in haemophilia A patients with high titre of inhibitor using a new brand recombinant factor VIIa (Aryoseven<sup>®</sup>).
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e451, doi. 10.1111/hae.13006
- By:
- Publication type:
- Article
Joint bleeds increase the inhibitor response to human factor VIII in a rat model of severe haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 772, doi. 10.1111/hae.13014
- By:
- Publication type:
- Article
Haemophilia registries to complement clinical trial data: a pious hope or an urgent necessity?
- Published in:
- 2016
- By:
- Publication type:
- Editorial
Practical aspects of psychological support to the patient with haemophilia from diagnosis in infancy through childhood and adolescence.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e349, doi. 10.1111/hae.13018
- By:
- Publication type:
- Article
Modelling lifelong effects of different prophylactic treatment strategies for severe haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e375, doi. 10.1111/hae.13019
- By:
- Publication type:
- Article
Use of donated clotting factors for surgeries on haemophilic patients in a resource-constrained country: a kind donor, good outcome, change of practice and future directions.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e453, doi. 10.1111/hae.13017
- By:
- Publication type:
- Article
An institutional pilot study to investigate physical activity patterns in boys with haemophilia.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e383, doi. 10.1111/hae.13021
- By:
- Publication type:
- Article
Platelet abnormalities in a family with von Willebrand disease type 2B (V1316M) and association with bleeding score.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e455, doi. 10.1111/hae.13026
- By:
- Publication type:
- Article
Major orthopaedic surgery for a haemophilia patient with inhibitors using a new bypassing agent.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e459, doi. 10.1111/hae.13029
- By:
- Publication type:
- Article
Inhibitor development in two cousins receiving full-length factor VIII (FVIII) and FVIII-Fc fusion protein.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e462, doi. 10.1111/hae.13032
- By:
- Publication type:
- Article
Activated prothrombin complex concentrate in combination with tranexamic acid: a single centre experience for the treatment of mucosal bleeding and dental extraction in haemophilia patients with inhibitors.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e465, doi. 10.1111/hae.13035
- By:
- Publication type:
- Article
Response to Wiewel-Verschueren S et al.: gynaecological and obstetrical bleeding in women with factor XI deficiency - a systematic review.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e435, doi. 10.1111/hae.13036
- By:
- Publication type:
- Article
A case of acquired haemophilia A complicated by peritonitis after distal gastrectomy.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e469, doi. 10.1111/hae.13039
- By:
- Publication type:
- Article
First preclinical support for the 'danger theory' in inhibitor development.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. 654, doi. 10.1111/hae.13042
- By:
- Publication type:
- Article
Successful bleeding control with recombinant porcine factor VIII in reduced loading doses in two patients with acquired haemophilia A and failure of bypassing agent therapy.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e472, doi. 10.1111/hae.13046
- By:
- Publication type:
- Article
Inhibitor development after liver transplantation in congenital factor VII deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e417, doi. 10.1111/hae.13047
- By:
- Publication type:
- Article
Efficacy of tranexamic acid for the prevention of bleeding in patients with von Willebrand disease and Glanzmann thrombasthenia: a controlled, before and after trial.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e423, doi. 10.1111/hae.13051
- By:
- Publication type:
- Article
A new parameter in the thrombin generation assay, mean velocity to peak thrombin, reflects factor VIII activity in patients with haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e474, doi. 10.1111/hae.13052
- By:
- Publication type:
- Article
Gynaecological and obstetrical bleeding in women with factor XI deficiency - a systematic review: response to rebuttal.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e436, doi. 10.1111/hae.13053
- By:
- Publication type:
- Article
Three successful deliveries involving a woman with congenital afibrinogenaemia - conventional fibrinogen concentrate infusion vs. 'as required' fibrinogen concentrate infusion based on changes in fibrinogen clearance -.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e478, doi. 10.1111/hae.13054
- By:
- Publication type:
- Article
Psychometric field testing of the HemoLatin-QoL questionnaire.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e390, doi. 10.1111/hae.13055
- By:
- Publication type:
- Article
Successful multivessel percutaneous coronary intervention for acute coronary syndrome in a HIV-positive severe haemophiliac.
- Published in:
- Haemophilia, 2016, v. 22, n. 5, p. e481, doi. 10.1111/hae.13056
- By:
- Publication type:
- Article