Works matching IS 13518216 AND DT 2010 AND VI 16 AND IP 5
Results: 18
An improved manufacturing process for Xyntha/ReFacto AF.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 717, doi. 10.1111/j.1365-2516.2009.02160.x
- By:
- Publication type:
- Article
Induction of immune tolerance using rituximab in a child with severe haemophilia B with inhibitors and anaphylaxis to factor IX.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Adenotonsillectomy in patients with desmopressin responsive mild bleeding disorders: a review of the literature.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 711, doi. 10.1111/j.1365-2516.2009.02145.x
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- Publication type:
- Article
Correlation of transient elastography with APRI and FIB-4 in a cohort of patients with congenital bleeding disorders and HCV or HIV/HCV coinfection.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 778, doi. 10.1111/j.1365-2516.2010.02204.x
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- Publication type:
- Article
How many carriers are there?
- Published in:
- 2010
- By:
- Publication type:
- Letter
Factor XI deficiency: two novel mutations in asymptomatic Italian patients.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 767, doi. 10.1111/j.1365-2516.2010.02241.x
- By:
- Publication type:
- Article
Natural progression of blood-induced joint damage in patients with haemophilia: clinical relevance and reproducibility of three-dimensional gait analysis.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 813, doi. 10.1111/j.1365-2516.2010.02245.x
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- Publication type:
- Article
Thrombin generation in patients with factor XI deficiency and clinical bleeding risk.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 771, doi. 10.1111/j.1365-2516.2010.02246.x
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- Publication type:
- Article
Arthrodesis of the ankle and subtalar joints in patients with haemophilic arthropathy.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 822, doi. 10.1111/j.1365-2516.2010.02248.x
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- Publication type:
- Article
Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 791, doi. 10.1111/j.1365-2516.2010.02228.x
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- Publication type:
- Article
Remission of paroxysmal atrial fibrillation with iron reduction in haemophilia A.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 726, doi. 10.1111/j.1365-2516.2010.02218.x
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- Publication type:
- Article
Continuous infusion during total joint arthroplasty in Japanese haemophilia A patients: comparison study among two recombinants and one plasma-derived factor VIII.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 740, doi. 10.1111/j.1365-2516.2010.02244.x
- By:
- Publication type:
- Article
Prevalence of allo-immunization anti-HLA and anti-integrin αIIbβ3 in Glanzmann Thromboasthenia patients.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 805, doi. 10.1111/j.1365-2516.2010.02230.x
- By:
- Publication type:
- Article
Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 747, doi. 10.1111/j.1365-2516.2010.02231.x
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- Publication type:
- Article
BDDrFVIII (Moroctocog alfa [AF-CC]) for surgical haemostasis in patients with haemophilia A: results of a pivotal study.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 731, doi. 10.1111/j.1365-2516.2010.02239.x
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- Publication type:
- Article
F8 mRNA studies in haemophilia A patients with different splice site mutations.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 786, doi. 10.1111/j.1365-2516.2010.02250.x
- By:
- Publication type:
- Article
Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 801, doi. 10.1111/j.1365-2516.2010.02268.x
- By:
- Publication type:
- Article
The impact of menstrual disorders on quality of life in women with inherited bleeding disorders.
- Published in:
- Haemophilia, 2010, v. 16, n. 5, p. 832, doi. 10.1111/j.1365-2516.2010.02269.x
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- Publication type:
- Article