Works matching IS 13518216 AND DT 2016 AND VI 22 AND IP 4
Results: 46
Efficacy and safety of long-acting recombinant fusion protein linking factor IX with albumin in haemophilia B patients undergoing surgery.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e259, doi. 10.1111/hae.12972
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- Article
Rituximab as first-line therapy for acquired haemophilia A: a single-centre 10-year experience.
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- Haemophilia, 2016, v. 22, n. 4, p. e338, doi. 10.1111/hae.12973
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- Article
Neutralizing capacity of inhibitors on FVIII is lower for natural FVIII/ VWF complex than for isolated FVIII: in vitro comparative study in eleven different therapeutic FVIII concentrates.
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- Haemophilia, 2016, v. 22, n. 4, p. e341, doi. 10.1111/hae.12975
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- Article
M1761K mutation in the von Willebrand factor A3 domain associated with impaired collagen binding and without platelet dysfunction.
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- Haemophilia, 2016, v. 22, n. 4, p. e345, doi. 10.1111/hae.12976
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- Article
Is there a role for antiangiogenic therapy, bevacizumab, in the treatment of recurrent digestive bleeding due to angiodysplasia in Glanzmann's thrombasthenia?
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- Haemophilia, 2016, v. 22, n. 4, p. e347, doi. 10.1111/hae.12977
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- Article
Haematuria is not a risk factor of hypertension or renal impairment in patients with haemophilia.
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- Haemophilia, 2016, v. 22, n. 4, p. 549, doi. 10.1111/hae.12921
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Evidence of pathogenicity of a mutation in 3′ untranslated region causing mild haemophilia A.
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- Haemophilia, 2016, v. 22, n. 4, p. 598, doi. 10.1111/hae.12923
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The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia A.
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- Haemophilia, 2016, v. 22, n. 4, p. e286, doi. 10.1111/hae.12927
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- Article
Improvement in health-related quality of life in patients with haemophilia B treated with nonacog beta pegol, a new extended half-life recombinant FIX product.
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- Haemophilia, 2016, v. 22, n. 4, p. e267, doi. 10.1111/hae.12995
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- Article
Pro- and anticoagulant factors facilitate thrombin generation and balance the haemostatic response to FEIBA<sup>®</sup> in prophylactic therapy.
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- Haemophilia, 2016, v. 22, n. 4, p. 615, doi. 10.1111/hae.12873
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- Article
Spontaneous splenic rupture accompanied by hepatic arterial dissection in a patient with autoimmune haemorrhaphilia due to anti-factor XIII antibodies.
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- Haemophilia, 2016, v. 22, n. 4, p. e314, doi. 10.1111/hae.12940
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- Article
Multimodal blood loss prevention approach including intra-articular tranexamic acid in primary total knee arthroplasty for patients with severe haemophilia A.
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- Haemophilia, 2016, v. 22, n. 4, p. e318, doi. 10.1111/hae.12942
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- Article
Improving comprehensive care in the haemophilia community: building on the HERO Study.
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- Haemophilia, 2016, v. 22, n. 4, p. e320, doi. 10.1111/hae.12945
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- Article
Laparoscopic surgery in a woman with factor V deficiency: revisiting platelet factor V.
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- Haemophilia, 2016, v. 22, n. 4, p. e322, doi. 10.1111/hae.12946
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- Article
Sodium content in products used to treat haemophilia.
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- Haemophilia, 2016, v. 22, n. 4, p. e324, doi. 10.1111/hae.12948
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Editorial Board.
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- Haemophilia, 2016, v. 22, n. 4, p. 475, doi. 10.1111/hae.12821
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- Article
Table of Contents.
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- Haemophilia, 2016, v. 22, n. 4, p. 477, doi. 10.1111/hae.12822
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- Article
Instructions for Authors.
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- Haemophilia, 2016, v. 22, n. 4, p. 634, doi. 10.1111/hae.12823
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- Article
Two new double mutant alleles of the F7 gene and a literature review on alleles with two mutations in FVII deficiency.
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- Haemophilia, 2016, v. 22, n. 4, p. e304, doi. 10.1111/hae.12897
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- Article
Themes in daily life of adolescents and young adults with congenital bleeding disorders: a qualitative study.
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- Haemophilia, 2016, v. 22, n. 4, p. e330, doi. 10.1111/hae.12961
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- Article
Efficacy and safety of pegylated full-length recombinant factor VIII with extended half-life for perioperative haemostasis in haemophilia A patients.
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- Haemophilia, 2016, v. 22, n. 4, p. e251, doi. 10.1111/hae.12963
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- Article
Extensive subcutaneous haematoma associated with transdermal analgesic patch in a haemophilia A patient with inhibitor.
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- Haemophilia, 2016, v. 22, n. 4, p. e333, doi. 10.1111/hae.12966
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- Article
Haemophilia and age-related comorbidities: do men with haemophilia consult a general practitioner for men's preventative health checks?
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- Haemophilia, 2016, v. 22, n. 4, p. e335, doi. 10.1111/hae.12968
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- Article
Successful use of tranexamic acid in the management of haemophilic pseudotumour.
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- Haemophilia, 2016, v. 22, n. 4, p. e306, doi. 10.1111/hae.12911
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- Article
The impact of sport on health status, psychological well-being and physical performance of adults with haemophilia.
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- Haemophilia, 2016, v. 22, n. 4, p. 521, doi. 10.1111/hae.12912
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- Article
Penny wise, pound foolish: an assessment of Canadian Hemophilia/inherited bleeding disorder comprehensive care program services and resources.
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- Haemophilia, 2016, v. 22, n. 4, p. 531, doi. 10.1111/hae.12913
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Correlation between FIX genotype and pharmacokinetics of Nonacog alpha according to a multicentre Italian study.
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- Haemophilia, 2016, v. 22, n. 4, p. 537, doi. 10.1111/hae.12916
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- Article
Congenital macrothrombocytopenia is a heterogeneous disorder in India.
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- Haemophilia, 2016, v. 22, n. 4, p. 570, doi. 10.1111/hae.12917
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- Article
Viral dynamic modelling of Hepatitis C and resistance-associated variants in haemophiliacs.
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- Haemophilia, 2016, v. 22, n. 4, p. 543, doi. 10.1111/hae.12918
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Identification of von Willebrand disease type 1 in a patient with Ehlers-Danlos syndrome classic type.
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- Haemophilia, 2016, v. 22, n. 4, p. e309, doi. 10.1111/hae.12931
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- Article
Declining trends in invasive orthopedic interventions for people with hemophilia enrolled in the Universal Data Collection program (2000-2010).
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- Haemophilia, 2016, v. 22, n. 4, p. 604, doi. 10.1111/hae.12932
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Defining adherence to prophylaxis in haemophilia.
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- Haemophilia, 2016, v. 22, n. 4, p. e311, doi. 10.1111/hae.12935
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The incidence, risk and functional outcomes of intracranial haemorrhage in children with inherited bleeding disorders at one haemophilia center.
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- Haemophilia, 2016, v. 22, n. 4, p. 556, doi. 10.1111/hae.12938
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- Article
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents.
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- Haemophilia, 2016, v. 22, n. 4, p. e292, doi. 10.1111/hae.12939
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The use of enhanced half-life coagulation factor concentrates in routine clinical practice: guidance from UKHCDO.
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- Haemophilia, 2016, v. 22, n. 4, p. 487, doi. 10.1111/hae.13013
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- Article
Joint distraction in advanced haemophilic ankle arthropathy.
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- Haemophilia, 2016, v. 22, n. 4, p. e301, doi. 10.1111/hae.12884
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- Article
Meta-analysis: outcomes of total knee arthroplasty in the haemophilia population.
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- Haemophilia, 2016, v. 22, n. 4, p. e275, doi. 10.1111/hae.12885
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Predictors of non-adherence to prescribed prophylactic clotting-factor treatment regimens among adolescent and young adults with a bleeding disorder.
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- Haemophilia, 2016, v. 22, n. 4, p. e245, doi. 10.1111/hae.12951
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- Article
A germline variant affects putative mi RNA-binding sites at the F8 3′ UTR and acts as a potential haemophilia A phenotype modifier in Southern Brazilian patients.
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- Haemophilia, 2016, v. 22, n. 4, p. e327, doi. 10.1111/hae.12953
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Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease.
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- Haemophilia, 2016, v. 22, n. 4, p. 564, doi. 10.1111/hae.12900
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- Article
Recombinant long-acting glyco PEGylated factor IX (nonacog beta pegol) in haemophilia B: assessment of target joints in multinational phase 3 clinical trials.
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- Haemophilia, 2016, v. 22, n. 4, p. 507, doi. 10.1111/hae.12902
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- Article
Promoting self-management and adherence during prophylaxis: evidence-based recommendations for haemophilia professionals.
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- Haemophilia, 2016, v. 22, n. 4, p. 499, doi. 10.1111/hae.12904
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Association of peak factor VIII levels and area under the curve with bleeding in patients with haemophilia A on every third day pharmacokinetic-guided prophylaxis.
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- Haemophilia, 2016, v. 22, n. 4, p. 514, doi. 10.1111/hae.12905
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Characterization of five associations of F8 missense mutations containing FVIII B domain mutations.
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- Haemophilia, 2016, v. 22, n. 4, p. 583, doi. 10.1111/hae.12906
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Development of a tail vein transection bleeding model in fully anaesthetized haemophilia A mice - characterization of two novel FVIII molecules.
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- Haemophilia, 2016, v. 22, n. 4, p. 625, doi. 10.1111/hae.12907
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Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders.
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- Haemophilia, 2016, v. 22, n. 4, p. 590, doi. 10.1111/hae.12908
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- Article