Works matching IS 13518216 AND DT 2011 AND VI 17 AND IP 5
Results: 59
Reduced early prophylaxis of children with haemophilia in a developing country, Turkey.
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- Haemophilia, 2011, v. 17, n. 5, p. e840, doi. 10.1111/j.1365-2516.2011.02581.x
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- Article
<sup>90</sup>Yttrium-hydroxyapatite: a new therapeutic option for radioactive synovectomy in haemophilic synovitis.
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- Haemophilia, 2011, v. 17, n. 5, p. e985, doi. 10.1111/j.1365-2516.2011.02497.x
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- Article
Postoperative paraneoplastic factor VIII auto-antibodies in patients with solid tumours.
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- Haemophilia, 2011, v. 17, n. 5, p. e889, doi. 10.1111/j.1365-2516.2011.02522.x
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- Article
Pharmacokinetics and ex vivo whole blood clot formation of a new recombinant FVIII (N8) in haemophilia A dogs.
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- Haemophilia, 2011, v. 17, n. 5, p. e963, doi. 10.1111/j.1365-2516.2011.02580.x
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- Article
Infection after total knee arthroplasty in haemophilic arthropathy with special emphasis on late infection.
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- Haemophilia, 2011, v. 17, n. 5, p. e831, doi. 10.1111/j.1365-2516.2011.02530.x
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- Article
Clinical experience with Optivate<sup>®</sup>, high-purity factor VIII (FVIII) product with von Willebrand factor (VWF) in young children with haemophilia A.
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- Haemophilia, 2011, v. 17, n. 5, p. 737, doi. 10.1111/j.1365-2516.2011.02600.x
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- Article
Parents Empowering Parents (PEP) Program: understanding its impact on the bleeding disorders community.
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- Haemophilia, 2011, v. 17, n. 5, p. e895, doi. 10.1111/j.1365-2516.2011.02512.x
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- Article
Analysis of five polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in the Brazilian population.
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- Haemophilia, 2011, v. 17, n. 5, p. e936, doi. 10.1111/j.1365-2516.2011.02592.x
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- Article
The use of the new ReFacto AF Laboratory Standard allows reliable measurement of FVIII:C levels in ReFacto AF mock plasma samples by a one-stage clotting assay.
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- Haemophilia, 2011, v. 17, n. 5, p. e958, doi. 10.1111/j.1365-2516.2011.02523.x
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Liver transplantation in the haemophilia patient.
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- Haemophilia, 2011, v. 17, n. 5, p. e981, doi. 10.1111/j.1365-2516.2011.02533.x
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The optimal mode of delivery for the haemophilia carrier expecting an affected infant: further considerations.
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- Haemophilia, 2011, v. 17, n. 5, p. 818, doi. 10.1111/j.1365-2516.2011.02505.x
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- Article
UKHCDO guidelines on the management of HCV in patients with hereditary bleeding disorders 2011.
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- Haemophilia, 2011, v. 17, n. 5, p. e877, doi. 10.1111/j.1365-2516.2011.02585.x
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- Article
A systematic review of the management and outcomes of pregnancy in Glanzmann thrombasthenia.
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- Haemophilia, 2011, v. 17, n. 5, p. e858, doi. 10.1111/j.1365-2516.2011.02516.x
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- Article
rFVIIa administered by continuous infusion during surgery in patients with severe congenital FVII deficiency.
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- Haemophilia, 2011, v. 17, n. 5, p. 764, doi. 10.1111/j.1365-2516.2011.02596.x
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A case of acquired haemophilia following H1N1 vaccination.
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- Haemophilia, 2011, v. 17, n. 5, p. 815, doi. 10.1111/j.1365-2516.2011.02493.x
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- Article
Ultrasonography in the monitoring of management of haemarthrosis.
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- Haemophilia, 2011, v. 17, n. 5, p. 826, doi. 10.1111/j.1365-2516.2011.02538.x
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- Article
Predictors of treatment difficulties and satisfaction with haemophilia therapy in adult patients.
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- Haemophilia, 2011, v. 17, n. 5, p. e901, doi. 10.1111/j.1365-2516.2011.02578.x
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- Article
Economical comparison of APCC vs. rFVIIa for mild-to-moderate bleeding episodes in haemophilia patients with inhibitors.
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- Haemophilia, 2011, v. 17, n. 5, p. e969, doi. 10.1111/j.1365-2516.2011.02589.x
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- Article
Joint health and functional ability in children with haemophilia who receive intensive replacement therapy.
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- Haemophilia, 2011, v. 17, n. 5, p. 783, doi. 10.1111/j.1365-2516.2011.02606.x
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- Article
Repeated infusions of VWF/FVIII concentrate: impact of VWF:FVIII ratio on FVIII trough and peak levels in a rabbit model.
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- Haemophilia, 2011, v. 17, n. 5, p. 808, doi. 10.1111/j.1365-2516.2011.02603.x
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Identification of factor VIII gene mutations in patients with severe haemophilia A in Venezuela: identification of seven novel mutations.
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- Haemophilia, 2011, v. 17, n. 5, p. e913, doi. 10.1111/j.1365-2516.2011.02500.x
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5th Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) 22-24 February 2012, Rome, Italy.
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- Haemophilia, 2011, v. 17, n. 5, p. 830, doi. 10.1111/j.1365-2516.2011.02614.x
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- Article
Pharmacokinetic study of minipooled solvent/detergent-filtered cryoprecipitate factor VIII.
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- Haemophilia, 2011, v. 17, n. 5, p. e884, doi. 10.1111/j.1365-2516.2011.02511.x
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Factor X deficiency and intracranial bleeding: who is at risk?
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- Haemophilia, 2011, v. 17, n. 5, p. 759, doi. 10.1111/j.1365-2516.2011.02591.x
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A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India.
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- Haemophilia, 2011, v. 17, n. 5, p. e928, doi. 10.1111/j.1365-2516.2011.02584.x
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Monitoring rFVIIa 90 μg kg<sup>−1</sup> dosing in haemophiliacs: comparing laboratory response using various whole blood assays over 6 h.
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- Haemophilia, 2011, v. 17, n. 5, p. e949, doi. 10.1111/j.1365-2516.2011.02492.x
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Adherence with haemophilia treatments: a survey of haemophilia healthcare professionals in Canada.
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- Haemophilia, 2011, v. 17, n. 5, p. 816, doi. 10.1111/j.1365-2516.2011.02502.x
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Three dominant-negative mutations in factor XI-deficient patients.
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- Haemophilia, 2011, v. 17, n. 5, p. e919, doi. 10.1111/j.1365-2516.2011.02519.x
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Habitual physical activity in Dutch children and adolescents with haemophilia.
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- Haemophilia, 2011, v. 17, n. 5, p. e906, doi. 10.1111/j.1365-2516.2011.02555.x
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Haemophilia Utilization Group Study - Part Va (HUGS Va): design, methods and baseline data.
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- Haemophilia, 2011, v. 17, n. 5, p. 729, doi. 10.1111/j.1365-2516.2011.02595.x
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- Article
Immune tolerance induction with a factor VIII concentrate containing von Willebrand factor (Haemoctin SDH<sup>®</sup>) in 14 patients with severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 5, p. e837, doi. 10.1111/j.1365-2516.2011.02577.x
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Presurgical pharmacokinetic analysis of a von Willebrand factor/factor VIII (VWF/FVIII) concentrate in patients with von Willebrand's disease (VWD) has limited value in dosing for surgery.
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- Haemophilia, 2011, v. 17, n. 5, p. 752, doi. 10.1111/j.1365-2516.2011.02583.x
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Role of exercise and physical activity on haemophilic arthropathy, fall prevention and osteoporosis.
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- Haemophilia, 2011, v. 17, n. 5, p. e870, doi. 10.1111/j.1365-2516.2011.02514.x
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An analysis of factors affecting the incidence of inhibitor formation in patients with congenital haemophilia in Japan.
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- Haemophilia, 2011, v. 17, n. 5, p. 771, doi. 10.1111/j.1365-2516.2011.02599.x
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The burden of HCV treatment in patients with inherited bleeding disorders.
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- Haemophilia, 2011, v. 17, n. 5, p. 791, doi. 10.1111/j.1365-2516.2011.02602.x
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The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern Iran.
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- Haemophilia, 2011, v. 17, n. 5, p. 820, doi. 10.1111/j.1365-2516.2011.02510.x
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Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
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- Haemophilia, 2011, v. 17, n. 5, p. e843, doi. 10.1111/j.1365-2516.2011.02590.x
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Stabilization of fibrin clots by activated prothrombin complex concentrate and tranexamic acid in FVIII inhibitor plasma.
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- Haemophilia, 2011, v. 17, n. 5, p. e944, doi. 10.1111/j.1365-2516.2011.02491.x
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Is a reduced intensity treatment with Rituximab effective in acquired haemophilia A?
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- Haemophilia, 2011, v. 17, n. 5, p. 817, doi. 10.1111/j.1365-2516.2011.02503.x
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FVIII administration in surgery.
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- Haemophilia, 2011, v. 17, n. 5, p. 828, doi. 10.1111/j.1365-2516.2011.02594.x
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- Article
Haemophilia management: time to get personal?
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- Haemophilia, 2011, v. 17, n. 5, p. 721, doi. 10.1111/j.1365-2516.2011.02517.x
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Successful eradication of inhibitor of late recurrence and other high risk prognostic factors in a patient with severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 5, p. e833, doi. 10.1111/j.1365-2516.2011.02571.x
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In-patient rehabilitation in haemophilic subjects with total knee arthroplasty.
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- Haemophilia, 2011, v. 17, n. 5, p. e999, doi. 10.1111/j.1365-2516.2011.02547.x
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Molecular analysis of severe factor XI deficiency in three Italian patients.
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- Haemophilia, 2011, v. 17, n. 5, p. e835, doi. 10.1111/j.1365-2516.2011.02576.x
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Evaluation of the host response to endotoxemia of FVIII and FIX deficient mice.
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- Haemophilia, 2011, v. 17, n. 5, p. 800, doi. 10.1111/j.1365-2516.2011.02598.x
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FVIII replacement in 12-day-old newborn with haemophilia A requiring surgical repair of D transposition of great arteries.
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- Haemophilia, 2011, v. 17, n. 5, p. 821, doi. 10.1111/j.1365-2516.2011.02518.x
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Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII.
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- Haemophilia, 2011, v. 17, n. 5, p. e923, doi. 10.1111/j.1365-2516.2011.02529.x
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Platelets significantly modify procoagulant activities in haemophilia A.
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- Haemophilia, 2011, v. 17, n. 5, p. 743, doi. 10.1111/j.1365-2516.2011.02601.x
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Re: low incidence of factor VIII inhibitors in PUPs during prophylaxis, on-demand treatment and surgical procedures, with Octanate<sup>®</sup>: interim report from an ongoing prospective clinical study.
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- Haemophilia, 2011, v. 17, n. 5, p. e847, doi. 10.1111/j.1365-2516.2011.02605.x
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Compound heterozygosity or heterozygosity with two mutations in cis on the same allele?
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- Haemophilia, 2011, v. 17, n. 5, p. e832, doi. 10.1111/j.1365-2516.2011.02531.x
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- Article