Works matching IS 13518216 AND DT 2019 AND VI 25 AND IP 5
Results: 34
Instructions for Authors.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 904, doi. 10.1111/hae.13579
- Publication type:
- Article
Unsuspected Lyme disease presenting in refractory haemophilic haemarthrosis.
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- Haemophilia, 2019, v. 25, n. 5, p. e331, doi. 10.1111/hae.13821
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Marstacimab, a tissue factor pathway inhibitor neutralizing antibody, improves coagulation parameters of ex vivo dosed haemophilic blood and plasmas.
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- Haemophilia, 2019, v. 25, n. 5, p. 797, doi. 10.1111/hae.13820
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Development and evaluation of appropriate, culturally adapted educational tools for Ivoirian patients with haemophilia, haemophilia carriers and their families.
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- Haemophilia, 2019, v. 25, n. 5, p. 838, doi. 10.1111/hae.13818
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- Article
The first reported case of acquired haemophilia A in which bleeding episodes were successfully treated via administration of a single‐dose mixture of activated factor VIIa/X.
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- Haemophilia, 2019, v. 25, n. 5, p. e350, doi. 10.1111/hae.13843
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- Article
Decreased bone mineral density and associated factors in severe haemophilia A patients: A case‐control study.
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- Haemophilia, 2019, v. 25, n. 5, p. e315, doi. 10.1111/hae.13836
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Inhibitors against rFVIIa in patients with severe congenital FVII deficiency: A case series.
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- Haemophilia, 2019, v. 25, n. 5, p. e345, doi. 10.1111/hae.13839
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Implementation and assessment of a self‐ and community‐based rehabilitation programme in patients with haemophilia from Côte d'Ivoire.
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- Haemophilia, 2019, v. 25, n. 5, p. 859, doi. 10.1111/hae.13833
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- Article
Joint comorbidities among Swedish carriers of haemophilia: A register‐based cohort study over 22 years.
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- Haemophilia, 2019, v. 25, n. 5, p. 845, doi. 10.1111/hae.13831
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Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors.
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- Haemophilia, 2019, v. 25, n. 5, p. e342, doi. 10.1111/hae.13827
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Assessing the supportive care needs of parents with a child with a bleeding disorder using the Parental Needs Scale for Rare Diseases (PNS‐RD): A single‐centre pilot study.
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- Haemophilia, 2019, v. 25, n. 5, p. 831, doi. 10.1111/hae.13826
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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review.
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- Haemophilia, 2019, v. 25, n. 5, p. 747, doi. 10.1111/hae.13825
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- Article
Using dried blood spots for variant analysis for patients with haemophilia.
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- Haemophilia, 2019, v. 25, n. 5, p. e339, doi. 10.1111/hae.13824
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- Article
Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases.
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- Haemophilia, 2019, v. 25, n. 5, p. e336, doi. 10.1111/hae.13823
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- Article
Safety and efficacy of emicizumab and other novel agents in newborns and infants.
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- Haemophilia, 2019, v. 25, n. 5, p. e334, doi. 10.1111/hae.13822
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Management of bleeding and invasive procedures in haemophilia A patients with inhibitor treated with emicizumab (Hemlibra<sup>®</sup>): Proposals from the French network on inherited bleeding disorders (MHEMO), the French Reference Centre on Haemophilia, in collaboration with the French Working Group on Perioperative Haemostasis (GIHP)
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 731, doi. 10.1111/hae.13817
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Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia.
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- Haemophilia, 2019, v. 25, n. 5, p. 738, doi. 10.1111/hae.13816
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Immune tolerance induction in paediatric patients with haemophilia A and inhibitors receiving emicizumab prophylaxis.
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- Haemophilia, 2019, v. 25, n. 5, p. 789, doi. 10.1111/hae.13819
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- Publication type:
- Article
Haemophilia home care: A qualitative evaluation study of the Be Involved infusion program.
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- Haemophilia, 2019, v. 25, n. 5, p. 807, doi. 10.1111/hae.13780
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Screening urinalysis demonstrates that haematuria is a frequent finding in persons with haemophilia treated at a paediatric haemophilia treatment centre.
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- Haemophilia, 2019, v. 25, n. 5, p. 782, doi. 10.1111/hae.13815
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Risk of osteoporotic fractures as a consequence of haemophilia: A nationwide population‐based cohort study.
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- Haemophilia, 2019, v. 25, n. 5, p. 876, doi. 10.1111/hae.13814
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- Publication type:
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A field study evaluating the activity of N8‐GP in spiked plasma samples at clinical haemostasis laboratories.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 893, doi. 10.1111/hae.13813
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- Publication type:
- Article
Multicentre evaluation of CK Prest<sup>®</sup> for assaying plasma levels of factor IX fused with albumin (Idelvion<sup>®</sup>).
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e327, doi. 10.1111/hae.13812
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Comparing objective and self‐reported measures of adherence in haemophilia.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 821, doi. 10.1111/hae.13811
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- Article
On‐pump CABG in a patient with severe factor V deficiency.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e324, doi. 10.1111/hae.13809
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- Publication type:
- Article
Intramuscular vaccination of haemophiliacs: Is it really a risk for bleeding?
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- Haemophilia, 2019, v. 25, n. 5, p. e322, doi. 10.1111/hae.13808
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- Publication type:
- Article
Perioperative haemostasis with full‐length, PEGylated, recombinant factor VIII with extended half‐life (rurioctocog alfa pegol) in patients with haemophilia A: Final results of a multicentre, single‐arm phase III trial.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 773, doi. 10.1111/hae.13807
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Impact of the Survey of Inhibitors in Plasma‐Product Exposed Toddlers (SIPPET) study and its post hoc analyses on clinical practice in the United States: A survey of Haemophilia and Thrombosis Research Society members.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 764, doi. 10.1111/hae.13806
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- Publication type:
- Article
HOw Patients view Extended half‐life products: Impressions from real‐world experience (The HOPE study).
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 814, doi. 10.1111/hae.13803
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Advanced magnetic resonance imaging of cartilage components in haemophilic joints reveals that cartilage hemosiderin correlates with joint deterioration.
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- Haemophilia, 2019, v. 25, n. 5, p. 851, doi. 10.1111/hae.13802
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- Publication type:
- Article
A novel, point‐of‐care, whole‐blood assay utilizing dielectric spectroscopy is sensitive to coagulation factor replacement therapy in haemophilia A patients.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 885, doi. 10.1111/hae.13799
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- Publication type:
- Article
Factor VIII prophylaxis effects outweigh other hemostasis contributors in predicting severe haemophilia A joint outcomes.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 867, doi. 10.1111/hae.13778
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- Article
Burden of mild haemophilia A: Systematic literature review.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 755, doi. 10.1111/hae.13777
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- Article
Issue Information.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 725, doi. 10.1111/hae.13580
- Publication type:
- Article