Works matching IS 13518216 AND DT 2013 AND VI 19 AND IP 5
Results: 37
A survey of patients with haemophilia to understand how they track product used at home.
- Published in:
- Haemophilia, 2013, v. 19, n. 5, p. e289, doi. 10.1111/hae.12170
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- Article
Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors - a thrombin generation-guided pilot study.
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- Haemophilia, 2013, v. 19, n. 5, p. 782, doi. 10.1111/hae.12181
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- Article
Quality of life in paediatric haemophilia A patients.
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- Haemophilia, 2013, v. 19, n. 5, p. e320, doi. 10.1111/hae.12226
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- Article
Colonoscopy in patients with haemophilia: the duration of clotting factor coverage must be adjusted to suit the procedure.
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- Haemophilia, 2013, v. 19, n. 5, p. e296, doi. 10.1111/hae.12174
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- Article
Quantification of perioperative changes in von Willebrand factor and factor VIII during elective orthopaedic surgery in normal individuals.
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- Haemophilia, 2013, v. 19, n. 5, p. 758, doi. 10.1111/hae.12185
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- Article
Results of the WIRK prospective, non-interventional observational study of recombinant activated factor VII ( rFVIIa) in patients with congenital haemophilia with inhibitors and other bleeding disorders.
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- Haemophilia, 2013, v. 19, n. 5, p. 679, doi. 10.1111/hae.12156
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- Article
Tamoxifen for recurrent bleeds due to angiodysplasia in von Willebrand's disease.
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- Haemophilia, 2013, v. 19, n. 5, p. e313, doi. 10.1111/hae.12196
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- Article
Health-related quality of life in patients with haemophilia and inhibitors on prophylaxis with anti-inhibitor complex concentrate: results from the Pro- FEIBA study.
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- Haemophilia, 2013, v. 19, n. 5, p. 736, doi. 10.1111/hae.12178
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- Article
Successful delivery in patients with severe congenital factor V deficiency: a study of five homozygous patients.
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- Haemophilia, 2013, v. 19, n. 5, p. e318, doi. 10.1111/hae.12210
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- Article
Impact of personality and depression on quality of life in patients with severe haemophilia in Korea.
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- Haemophilia, 2013, v. 19, n. 5, p. e270, doi. 10.1111/hae.12221
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- Article
Erik von Willebrand.
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- Haemophilia, 2013, v. 19, n. 5, p. 643, doi. 10.1111/hae.12243
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- Article
Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency.
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- Haemophilia, 2013, v. 19, n. 5, p. e304, doi. 10.1111/hae.12180
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- Article
Are the standard definitions of osteopenia and osteoporosis appropriate for coinfected patients with haemophilia?
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- Haemophilia, 2013, v. 19, n. 5, p. e316, doi. 10.1111/hae.12207
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- Article
Factor VIII mutation and desmopressin-responsiveness in 62 patients with mild haemophilia A.
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- Haemophilia, 2013, v. 19, n. 5, p. 720, doi. 10.1111/hae.12173
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- Article
The experience of girls and young Women with inherited bleeding disorders.
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- Haemophilia, 2013, v. 19, n. 5, p. e276, doi. 10.1111/hae.12155
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- Article
Estimating unknown parameters in haemophilia using expert judgement elicitation.
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- Haemophilia, 2013, v. 19, n. 5, p. e282, doi. 10.1111/hae.12166
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- Article
Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene - a case report.
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- Haemophilia, 2013, v. 19, n. 5, p. e310, doi. 10.1111/hae.12190
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- Article
Consequences of switching from prophylactic treatment to on-demand treatment in late teens and early adults with severe haemophilia A: the TEEN/TWEN study.
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- Haemophilia, 2013, v. 19, n. 5, p. 727, doi. 10.1111/hae.12177
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- Article
Head-to-head comparison of the pharmacokinetic profiles of a high-purity factor IX concentrate (AlphaNine<sup>®</sup>) and a recombinant factor IX (BeneFIX<sup>®</sup>) in patients with severe haemophilia B.
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- Haemophilia, 2013, v. 19, n. 5, p. 674, doi. 10.1111/hae.12148
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- Article
Purchasing factor concentrates in the 21st century through competitive tendering.
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- Haemophilia, 2013, v. 19, n. 5, p. 660, doi. 10.1111/hae.12169
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- Article
Results from a large multinational clinical trial (guardian™1) using prophylactic treatment with turoctocog alfa in adolescent and adult patients with severe haemophilia A: safety and efficacy.
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- Haemophilia, 2013, v. 19, n. 5, p. 691, doi. 10.1111/hae.12159
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- Article
Advances in the treatment of inherited coagulation disorders.
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- Haemophilia, 2013, v. 19, n. 5, p. 648, doi. 10.1111/hae.12137
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- Article
RODIN and the pitfalls of observational studies.
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- Haemophilia, 2013, v. 19, n. 5, p. e315, doi. 10.1111/hae.12206
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- Article
Detection of new mutations and molecular pathology of mild and moderate haemophilia A patients from southern Brazil.
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- Haemophilia, 2013, v. 19, n. 5, p. 773, doi. 10.1111/hae.12172
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- Article
Population pharmacokinetics of recombinant factor IX: implications for dose tailoring.
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- Haemophilia, 2013, v. 19, n. 5, p. 753, doi. 10.1111/hae.12188
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- Article
Successful management of bilateral total hip replacement in a patient with von Willebrand's disease and developmental hip dysplasia.
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- Haemophilia, 2013, v. 19, n. 5, p. e306, doi. 10.1111/hae.12183
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- Article
A novel homozygous missense mutation in the factor VII gene of severe factor VII deficiency in a pedigree: a description of two cases.
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- Haemophilia, 2013, v. 19, n. 5, p. e298, doi. 10.1111/hae.12176
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- Article
Establishing a harmonized haemophilia registry for countries with developing health care systems.
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- Haemophilia, 2013, v. 19, n. 5, p. 668, doi. 10.1111/hae.12147
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- Article
Vitamin D deficiency in patients with haemophilia: an underestimated commorbidity.
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- Haemophilia, 2013, v. 19, n. 5, p. e308, doi. 10.1111/hae.12187
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- Article
Inhibitors in haemophilia B: the Italian experience.
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- Haemophilia, 2013, v. 19, n. 5, p. 686, doi. 10.1111/hae.12158
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- Article
Results from a large multinational clinical trial (guardian™3) using prophylactic treatment with turoctocog alfa in paediatric patients with severe haemophilia A: safety, efficacy and pharmacokinetics.
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- Haemophilia, 2013, v. 19, n. 5, p. 698, doi. 10.1111/hae.12165
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- Article
Use of global assays to understand clinical phenotype in congenital factor VII deficiency.
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- Haemophilia, 2013, v. 19, n. 5, p. 765, doi. 10.1111/hae.12160
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- Article
Bypass therapy assay testing as a strategy to reduce costs for treatment of haemophilia patients with inhibitors.
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- Haemophilia, 2013, v. 19, n. 5, p. 711, doi. 10.1111/hae.12171
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- Article
Obesity in haemophilia patients: effect on bleeding frequency, clotting factor concentrate usage, and haemostatic and fibrinolytic parameters.
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- Haemophilia, 2013, v. 19, n. 5, p. 744, doi. 10.1111/hae.12182
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- Article
Impact of HLA alleles and cytokine polymorphisms on inhibitors development in children with severe haemophilia A.
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- Haemophilia, 2013, v. 19, n. 5, p. 706, doi. 10.1111/hae.12168
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- Article
Rapid musculoskeletal ultrasound for painful episodes in adult haemophilia patients.
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- Haemophilia, 2013, v. 19, n. 5, p. 790, doi. 10.1111/hae.12175
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- Article
Two haemophilia patients with inhibitors who became ambulatory after physiotherapy under haemostatic cover with bypassing agents.
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- Haemophilia, 2013, v. 19, n. 5, p. e301, doi. 10.1111/hae.12179
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- Article