Works matching IS 13518216 AND DT 2015 AND VI 21 AND IP 2
Results: 27
Molecular characterization of ten F8 splicing mutations in RNA isolated from patient's leucocytes: assessment of in silico prediction tools accuracy.
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- Haemophilia, 2015, v. 21, n. 2, p. 249, doi. 10.1111/hae.12562
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- Article
The incidence of factor VIII inhibitors in severe haemophilia A following a major switch from full-length to B-domain-deleted factor VIII: a prospective cohort comparison.
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- Haemophilia, 2015, v. 21, n. 2, p. 219, doi. 10.1111/hae.12563
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Improved prediction of inhibitor development in previously untreated patients with severe haemophilia A.
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- Haemophilia, 2015, v. 21, n. 2, p. 227, doi. 10.1111/hae.12566
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Controlled, cross-sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand.
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- Haemophilia, 2015, v. 21, n. 2, p. 171, doi. 10.1111/hae.12539
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The development of pulmonary embolus in patients with haemophilia A and high-titre inhibitors - a case series and review of the literature.
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- Haemophilia, 2015, v. 21, n. 2, p. e134, doi. 10.1111/hae.12600
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- Article
Characterization of a novel mutation in F8 gene causing severe haemophilia A by deletion mapping with STS markers.
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- Haemophilia, 2015, v. 21, n. 2, p. e136, doi. 10.1111/hae.12607
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Orthomolecular nutritional therapy for plasminogen deficiency: report of a case that showed positive results.
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- Haemophilia, 2015, v. 21, n. 2, p. e139, doi. 10.1111/hae.12609
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- Article
Pharmacokinetics of plasma-derived vs. recombinant FVIII concentrates: a comparative study.
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- Haemophilia, 2015, v. 21, n. 2, p. 204, doi. 10.1111/hae.12550
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Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B.
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- Haemophilia, 2015, v. 21, n. 2, p. 210, doi. 10.1111/hae.12553
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Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency.
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- Haemophilia, 2015, v. 21, n. 2, p. 241, doi. 10.1111/hae.12554
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Recombinant factor VIIa enhances platelet deposition from flowing haemophilic blood but requires the contact pathway to promote fibrin deposition.
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- Haemophilia, 2015, v. 21, n. 2, p. 266, doi. 10.1111/hae.12558
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Identification of six novel F9 mutations among haemophilia B patients from Macedonia and Bulgaria.
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- Haemophilia, 2015, v. 21, n. 2, p. e144, doi. 10.1111/hae.12620
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- Article
Home-delivered ultrasound monitoring for home treatment of haemarthrosis in haemophilia A.
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- Haemophilia, 2015, v. 21, n. 2, p. e147, doi. 10.1111/hae.12622
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- Article
Efficacy and safety of OBI-1, an antihaemophilic factor VIII (recombinant), porcine sequence, in subjects with acquired haemophilia A.
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- Haemophilia, 2015, v. 21, n. 2, p. 162, doi. 10.1111/hae.12627
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Monitoring bypassing agent therapy - a prospective crossover study comparing thromboelastometry and thrombin generation assay.
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- Haemophilia, 2015, v. 21, n. 2, p. 275, doi. 10.1111/hae.12570
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- Article
Oral surgery-associated postoperative bleeding in haemophilia patients - a tertiary centre's two decade experience.
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- Haemophilia, 2015, v. 21, n. 2, p. 234, doi. 10.1111/hae.12573
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- Article
Prospective, observational study of plasma-derived factor VIII/von Willebrand factor in immune tolerance induction: the PRISM registry.
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- Haemophilia, 2015, v. 21, n. 2, p. e122, doi. 10.1111/hae.12590
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- Article
Individualized factor IX dosing in two brothers: application of longitudinal pharmacokinetic modelling to optimize therapeutic benefit.
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- Haemophilia, 2015, v. 21, n. 2, p. e125, doi. 10.1111/hae.12593
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- Article
Robotic coronary artery bypass surgery in a patient with haemophilia A.
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- Haemophilia, 2015, v. 21, n. 2, p. e128, doi. 10.1111/hae.12594
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- Article
Haemophilia-related outcome after liver transplantation and treatment with sofosbuvir/ribavirin in a HCV- HIV coinfected man with liver failure and hepatocellular carcinoma.
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- Haemophilia, 2015, v. 21, n. 2, p. e131, doi. 10.1111/hae.12599
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Preliminary results for the use of knee mega-endoprosthesis in the treatment of musculoskeletal complications of haemophilia.
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- Haemophilia, 2015, v. 21, n. 2, p. 258, doi. 10.1111/hae.12541
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Treatment decision-making among Canadian youth with severe haemophilia: a qualitative approach.
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- Haemophilia, 2015, v. 21, n. 2, p. 180, doi. 10.1111/hae.12543
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Correlation between dispensed and prescribed doses of factor products for bleeding disorders: can a small, centre-based pharmacy hit the mark?
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- Haemophilia, 2015, v. 21, n. 2, p. 190, doi. 10.1111/hae.12546
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Recombinant factor IX ( BAX326.
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- Haemophilia, 2015, v. 21, n. 2, p. 196, doi. 10.1111/hae.12548
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- Article
Recombinant porcine factor VIII: a new instalment of a long story.
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- Haemophilia, 2015, v. 21, n. 2, p. 149, doi. 10.1111/hae.12612
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Novel therapeutic approaches for haemophilia.
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- Haemophilia, 2015, v. 21, n. 2, p. 152, doi. 10.1111/hae.12615
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Estimation of tensile properties of the Achilles tendon in haemophilic arthropathy of the ankle: case study.
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- Haemophilia, 2015, v. 21, n. 2, p. e141, doi. 10.1111/hae.12619
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- Article