Works matching IS 13518216 AND DT 2019 AND VI 25
Results: 243
Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland.
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- Haemophilia, 2019, v. 25, n. 6, p. e373, doi. 10.1111/hae.13854
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Current dosing practices for perioperative factor VIII concentrate treatment in mild haemophilia A patients result in FVIII levels above target.
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- Haemophilia, 2019, v. 25, n. 6, p. 960, doi. 10.1111/hae.13838
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Mothers' intentions and behaviours regarding providing risk communication to their daughters about their possibility of being haemophilia carriers: A qualitative study.
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- Haemophilia, 2019, v. 25, n. 6, p. 1059, doi. 10.1111/hae.13864
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Concizumab promotes haemostasis via a tissue factor‐factor VIIa–dependent mechanism supporting prophylactic treatment of haemophilia: Results from a rabbit haemophilia bleeding model.
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- Haemophilia, 2019, v. 25, n. 6, p. e379, doi. 10.1111/hae.13861
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Measurement of plasma and platelet tissue factor pathway inhibitor, factor V and Protein S in people with haemophilia.
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- Haemophilia, 2019, v. 25, n. 6, p. 1083, doi. 10.1111/hae.13860
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Effects of exercise in people with haemophilia: An umbrella review of systematic reviews and meta‐analyses.
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- Haemophilia, 2019, v. 25, n. 6, p. 928, doi. 10.1111/hae.13868
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Instructions for Authors.
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- Haemophilia, 2019, v. 25, n. 5, p. 904, doi. 10.1111/hae.13579
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- Article
A novel protocol for accurate and reliable postoperative bolus administration of recombinant factor VIIa using an automated mini‐pump system.
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- Haemophilia, 2019, v. 25, n. 6, p. 1020, doi. 10.1111/hae.13863
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Immune tolerance induction with moroctocog‐alpha (Refacto/Refacto AF) in a population of Italian haemophilia A patients with high‐titre inhibitors: Data from REF.IT Registry.
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- Haemophilia, 2019, v. 25, n. 6, p. 1003, doi. 10.1111/hae.13859
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Haemophilic arthropathy: A narrative review on the use of intra‐articular drugs for arthritis.
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- Haemophilia, 2019, v. 25, n. 6, p. 919, doi. 10.1111/hae.13857
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Mechanistic rationale for factor XIII cotreatment in haemophilia.
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- Haemophilia, 2019, v. 25, n. 6, p. e377, doi. 10.1111/hae.13855
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Real‐life experience in switching to new extended half‐life products at European haemophilia centres.
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- Haemophilia, 2019, v. 25, n. 6, p. 946, doi. 10.1111/hae.13834
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The Paediatric Haemophilia Activities List (pedHAL) in routine assessment: changes over time, child‐parent agreement and informative domains.
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- Haemophilia, 2019, v. 25, n. 6, p. 953, doi. 10.1111/hae.13835
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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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BAY 94‐9027 prophylaxis is efficacious and well tolerated for up to >5 years with extended dosing intervals: PROTECT VIII extension interim results.
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- Haemophilia, 2019, v. 25, n. 6, p. 1011, doi. 10.1111/hae.13853
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Individual combinations of danger signals synergistically increase FVIII product immunogenicity.
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- Haemophilia, 2019, v. 25, n. 6, p. 996, doi. 10.1111/hae.13852
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A rare cause of bleeding in two Indian families with congenital alpha‐2‐antiplasmin deficiency.
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- Haemophilia, 2019, v. 25, n. 6, p. e370, doi. 10.1111/hae.13851
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Disease‐related distress among adults with haemophilia: A qualitative study.
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- Haemophilia, 2019, v. 25, n. 6, p. 988, doi. 10.1111/hae.13850
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A child with haemophilia A and Shwachman‐Diamond syndrome with literature review of combined haematologic diseases in children.
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- Haemophilia, 2019, v. 25, n. 6, p. e368, doi. 10.1111/hae.13849
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A multicentre, open‐label study of emicizumab given every 2 or 4 weeks in children with severe haemophilia A without inhibitors.
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- Haemophilia, 2019, v. 25, n. 6, p. 979, doi. 10.1111/hae.13848
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Potential of the Community Counts registry to characterize rare bleeding disorders.
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- Haemophilia, 2019, v. 25, n. 6, p. 1045, doi. 10.1111/hae.13847
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Severe postpartum haemorrhage as first presenting symptom of an inherited bleeding disorder.
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- Haemophilia, 2019, v. 25, n. 6, p. 1051, doi. 10.1111/hae.13846
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The evolution of factor VIIa in the treatment of bleeding in haemophilia with inhibitors.
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- Haemophilia, 2019, v. 25, n. 6, p. 911, doi. 10.1111/hae.13845
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Clinical evaluation of bleeds and response to haemostatic treatment in patients with acquired haemophilia: A global expert consensus statement.
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- Haemophilia, 2019, v. 25, n. 6, p. 969, doi. 10.1111/hae.13844
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Thrombin and plasmin generation in patients with plasminogen or plasminogen activator inhibitor type 1 deficiency.
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- Haemophilia, 2019, v. 25, n. 6, p. 1073, doi. 10.1111/hae.13842
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Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease.
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- Haemophilia, 2019, v. 25, n. 6, p. 1035, doi. 10.1111/hae.13841
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Physiotherapy outcome measures of haemophilia acute bleed episodes: What matters to patients?
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- Haemophilia, 2019, v. 25, n. 6, p. 1066, doi. 10.1111/hae.13840
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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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Nutritional status of children and adolescents with haemophilia in Basra, Iraq.
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- Haemophilia, 2019, v. 25, n. 6, p. e353, doi. 10.1111/hae.13837
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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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Patient‐centred care in haemophilia: Patient perspectives on visualization and participation in decision‐making.
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- Haemophilia, 2019, v. 25, n. 6, p. 938, doi. 10.1111/hae.13830
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Elimination of hepatitis C virus infection in patients with haemophilia in Belgium: A single‐centre experience.
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- Haemophilia, 2019, v. 25, n. 6, p. 1028, doi. 10.1111/hae.13829
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Pharmacokinetics of a new human plasma‐derived double virus inactivated and nanofiltered factor IX concentrate in previously treated severe or moderately severe haemophilia B patients.
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- Haemophilia, 2019, v. 25, n. 6, p. e364, doi. 10.1111/hae.13828
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FVIII dosages in persons with haemophilia A treated with extended half‐life products: From local biology to optimized patient management.
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- Haemophilia, 2019, v. 25, n. 6, p. e361, doi. 10.1111/hae.13801
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Issue Information.
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- Haemophilia, 2019, v. 25, n. 6, p. 905, doi. 10.1111/hae.13582
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- Article
Instructions for Authors.
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- Haemophilia, 2019, v. 25, n. 6, p. 1092, doi. 10.1111/hae.13581
- Publication type:
- Article
Author Index.
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- Haemophilia, 2019, v. 25, p. 20, doi. 10.1111/hae.13667
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- Article
Issue Information.
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- Haemophilia, 2019, v. 25, p. 1, doi. 10.1111/hae.13661
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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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Abstracts.
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- Haemophilia, 2019, v. 25, p. 3, doi. 10.1111/hae.13786
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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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Outpatient treatment for haemophilic arthropathy with radiosynovectomy: Radiation dose to family members.
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- Haemophilia, 2019, v. 25, n. 3, p. 509, doi. 10.1111/hae.13710
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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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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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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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