Works matching IS 13518216 AND DT 2015 AND VI 21 AND IP 6
Results: 43
Haemophilia A carriers experience reduced health-related quality of life.
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- Haemophilia, 2015, v. 21, n. 6, p. 761, doi. 10.1111/hae.12690
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Point of care ultrasonography in haemophilia care: recommendations for training and competency evaluation.
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- Haemophilia, 2015, v. 21, n. 6, p. 828, doi. 10.1111/hae.12767
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Cardiovascular disease (CVD) in Canadians with haemophilia: Age-Related CVD in Haemophilia Epidemiological Research (ARCHER study).
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- Haemophilia, 2015, v. 21, n. 6, p. 736, doi. 10.1111/hae.12768
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Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families.
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- Haemophilia, 2015, v. 21, n. 6, p. e519, doi. 10.1111/hae.12788
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Mitral valve repair in a Jehovah's witness with haemophilia A with high-titre inhibitor.
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- Haemophilia, 2015, v. 21, n. 6, p. e523, doi. 10.1111/hae.12789
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Pharmacokinetic properties of BAY 81-8973, a full-length recombinant factor VIII.
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- Haemophilia, 2015, v. 21, n. 6, p. 766, doi. 10.1111/hae.12691
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A diagnostic dilemma: variant Bernard-Soulier syndrome, a difficult clinical and genetic diagnosis.
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- Haemophilia, 2015, v. 21, n. 6, p. e510, doi. 10.1111/hae.12777
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Age-related factor IX correction in symptomatic female carriers with haemophilia B Leyden.
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- Haemophilia, 2015, v. 21, n. 6, p. e498, doi. 10.1111/hae.12761
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Factor for felons: how can we provide haemophilia care to the incarcerated?
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- Haemophilia, 2015, v. 21, n. 6, p. 772, doi. 10.1111/hae.12711
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Bilateral upper limb compartment syndrome induced by strenuous exercise in a patient with haemophilia A and a low titre inhibitor.
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- Haemophilia, 2015, v. 21, n. 6, p. e517, doi. 10.1111/hae.12783
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Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
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- Haemophilia, 2015, v. 21, n. 6, p. 846, doi. 10.1111/hae.12712
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Oral health in children and adolescents with haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. 778, doi. 10.1111/hae.12717
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Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature.
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- Haemophilia, 2015, v. 21, n. 6, p. 820, doi. 10.1111/hae.12719
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A tortuous route to a capable fatherhood: the experience of being a father to a child with severe haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. 799, doi. 10.1111/hae.12781
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Long-handle toothbrush for haemophiliacs with severe elbow arthropathy.
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- Haemophilia, 2015, v. 21, n. 6, p. e481, doi. 10.1111/hae.12751
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Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery.
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- Haemophilia, 2015, v. 21, n. 6, p. e513, doi. 10.1111/hae.12782
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Complications associated with central venous access device in children with haemophilia: a nationwide multicentre study in Finland.
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- Haemophilia, 2015, v. 21, n. 6, p. 747, doi. 10.1111/hae.12665
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Lupus anticoagulant acquired hypoprothrombinemia syndrome in childhood: two distinct patterns and review of the literature.
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- Haemophilia, 2015, v. 21, n. 6, p. 754, doi. 10.1111/hae.12669
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Utility of a Paediatric Bleeding Questionnaire as a screening tool for von Willebrand disease in apparently healthy children.
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- Haemophilia, 2015, v. 21, n. 6, p. 806, doi. 10.1111/hae.12689
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A systematic review of definitions and reporting of bleeding outcome measures in haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. 731, doi. 10.1111/hae.12750
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Inflammatory focal bone destruction in femoral heads with end-stage haemophilic arthropathy: a study on clinic samples with micro- CT and histological analyses.
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- Haemophilia, 2015, v. 21, n. 6, p. e472, doi. 10.1111/hae.12808
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Factor IX-deficient plasma spiked with N9-GP behaves similarly to N9-GP post-administration clinical samples in N9-GP ELISA and FIX activity assays.
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- Haemophilia, 2015, v. 21, n. 6, p. 832, doi. 10.1111/hae.12680
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Giant haemophilic pseudotumour of the pelvis: case report and literature review.
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- Haemophilia, 2015, v. 21, n. 6, p. e484, doi. 10.1111/hae.12752
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Response to Gringeri et al.: 'recombinant full-length factor VIII (FVIII) and extended half-life FVIII products in prophylaxis - new insight provided by pharmacokinetic modelling'.
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- Haemophilia, 2015, v. 21, n. 6, p. e489, doi. 10.1111/hae.12754
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Management of a myocardial infarction in a patient with classical acquired haemophilia patient in partial remission.
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- Haemophilia, 2015, v. 21, n. 6, p. e494, doi. 10.1111/hae.12757
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The first case report of a patient with simultaneous haemophilia A and accelerated phase chronic myelogenous leukaemia.
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- Haemophilia, 2015, v. 21, n. 6, p. e507, doi. 10.1111/hae.12776
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Results of a phase I/II open-label, safety and efficacy trial of coagulation factor IX (recombinant), albumin fusion protein in haemophilia B patients.
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- Haemophilia, 2015, v. 21, n. 6, p. 784, doi. 10.1111/hae.12721
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Pain management strategies in adults with haemophilia: a retrospective study.
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- Haemophilia, 2015, v. 21, n. 6, p. e487, doi. 10.1111/hae.12753
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Successful abdominal operation without replacement therapy in a patient with combined factor V (FV) and FVIII deficiency due to novel homozygous mutation in LMAN1.
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- Haemophilia, 2015, v. 21, n. 6, p. e492, doi. 10.1111/hae.12756
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Acquired haemophilia and the New Oral Anticoagulants (NOACs): coincidence or drug-induced adverse event?
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- Haemophilia, 2015, v. 21, n. 6, p. e496, doi. 10.1111/hae.12758
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Long-term prophylaxis in severe factor VII deficiency.
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- Haemophilia, 2015, v. 21, n. 6, p. 812, doi. 10.1111/hae.12702
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Comparison of several von Willebrand factor ( VWF) activity assays for monitoring patients undergoing treatment with VWF/ FVIII concentrates: improved performance with a new modified automated method.
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- Haemophilia, 2015, v. 21, n. 6, p. 837, doi. 10.1111/hae.12703
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Percutaneous transluminal aortic valve implantation for severe aortic valve stenosis in a patient with severe haemophilia A.
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- Haemophilia, 2015, v. 21, n. 6, p. e500, doi. 10.1111/hae.12771
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Motivational effects of top-rope climbing therapy under individualized prophylaxis: a pilot study in young adults with severe haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. e504, doi. 10.1111/hae.12773
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Classification and regression tree analysis vs. multivariable linear and logistic regression methods as statistical tools for studying haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. 715, doi. 10.1111/hae.12778
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Integrated analysis of safety data from 12 clinical interventional studies of plasma- and albumin-free recombinant factor VIII (r AHF- PFM) in haemophilia A.
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- Haemophilia, 2015, v. 21, n. 6, p. 791, doi. 10.1111/hae.12724
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The current role of orthoses in treating haemophilic arthropathy.
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- Haemophilia, 2015, v. 21, n. 6, p. 723, doi. 10.1111/hae.12779
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Association between bleeding tendency and health-related quality of life in carriers of moderate and severe haemophilia.
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- Haemophilia, 2015, v. 21, n. 6, p. 742, doi. 10.1111/hae.12796
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Should anti-inhibitor coagulant complex and tranexamic acid be used concomitantly?
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- Haemophilia, 2015, v. 21, n. 6, p. 709, doi. 10.1111/hae.12723
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WFH Musculoskeletal Congress 2015 Abstracts.
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- Haemophilia, 2015, v. 21, n. 6, p. e526, doi. 10.1111/hae.12794
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- Article
Distress in patients with bleeding disorders: a single institutional cross-sectional study.
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- Haemophilia, 2015, v. 21, n. 6, p. e456, doi. 10.1111/hae.12748
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Korea hemophilia foundation registry trends 1991-2012: patient registry, demographics, health services utilization.
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- Haemophilia, 2015, v. 21, n. 6, p. e479, doi. 10.1111/hae.12744
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Knowledge and attitudes survey in bleeding disorders providers regarding pain.
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- Haemophilia, 2015, v. 21, n. 6, p. e465, doi. 10.1111/hae.12749
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