Works matching IS 13518216 AND DT 2011 AND VI 17 AND IP 6
Results: 29
Elective orthopaedic surgery for haemophilia patients with inhibitors: single centre experience of 40 procedures and review of the literature.
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- Haemophilia, 2011, v. 17, n. 6, p. 910, doi. 10.1111/j.1365-2516.2011.02504.x
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Deep venous thrombosis screening in patients with inherited bleeding disorders and central venous catheters.
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- Haemophilia, 2011, v. 17, n. 6, p. 890, doi. 10.1111/j.1365-2516.2011.02515.x
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Evaluation of the overall haemostatic effect of recombinant factor VIIa by measuring thrombin generation and stability of fibrin clots.
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- Haemophilia, 2011, v. 17, n. 6, p. 957, doi. 10.1111/j.1365-2516.2011.02526.x
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Non-invasive tool for foetal sex determination in early gestational age.
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- Haemophilia, 2011, v. 17, n. 6, p. 952, doi. 10.1111/j.1365-2516.2011.02537.x
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Pharmacokinetics, pharmacodynamics and safety of recombinant canine FVIIa in a study dosing one haemophilia A and one haemostatically normal dog.
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- Haemophilia, 2011, v. 17, n. 6, p. 962, doi. 10.1111/j.1365-2516.2011.02536.x
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The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products.
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- Haemophilia, 2011, v. 17, n. 6, p. 931, doi. 10.1111/j.1365-2516.2011.02508.x
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Factor VII deficiency in pregnancy and delivery: a case report.
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- Haemophilia, 2011, v. 17, n. 6, p. e1005, doi. 10.1111/j.1365-2516.2011.02532.x
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Impact of lifestyle modification on symptomatic coronary artery disease in a haemophilia patient with inhibitors.
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- Haemophilia, 2011, v. 17, n. 6, p. e1006, doi. 10.1111/j.1365-2516.2011.02543.x
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The role of recombinant factor VIIa for obstetric block in women with severe factor XI deficiency.
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- Haemophilia, 2011, v. 17, n. 6, p. 906, doi. 10.1111/j.1365-2516.2011.02525.x
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Corrigenda.
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- Haemophilia, 2011, v. 17, n. 6, p. 979, doi. 10.1111/j.1365-2516.2011.02639.x
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- Article
Correlation between musculoskeletal function and radiological joint scores in haemophilia A adolescents.
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- Haemophilia, 2011, v. 17, n. 6, p. 920, doi. 10.1111/j.1365-2516.2011.02496.x
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Sexual evaluation and treatment of ageing males with haemophilia.
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- Haemophilia, 2011, v. 17, n. 6, p. 875, doi. 10.1111/j.1365-2516.2011.02507.x
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Bioequivalence between two serum-free recombinant factor VIII preparations (N8 and ADVATE<sup>®</sup>) - an open-label, sequential dosing pharmacokinetic study in patients with severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 6, p. 854, doi. 10.1111/j.1365-2516.2011.02495.x
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Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis.
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- Haemophilia, 2011, v. 17, n. 6, p. 944, doi. 10.1111/j.1365-2516.2011.02499.x
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Answer to 'a few notes of precaution'.
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- Haemophilia, 2011, v. 17, n. 6, p. e1008, doi. 10.1111/j.1365-2516.2011.02652.x
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Pharmacokinetics of VWF/FVIII concentrates is a very intricate matter.
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- Haemophilia, 2011, v. 17, n. 6, p. 846, doi. 10.1111/j.1365-2516.2011.02663.x
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Previously unrecognized advanced liver disease unveiled by transient elastography in patients with Haemophilia and chronic hepatitis C.
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- Haemophilia, 2011, v. 17, n. 6, p. 938, doi. 10.1111/j.1365-2516.2011.02520.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. 6, p. 980, doi. 10.1111/j.1365-2516.2011.02634.x
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- Article
Magnetic resonance imaging in teenagers and young adults with limited haemophilic arthropathy: baseline results from a prospective study.
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- Haemophilia, 2011, v. 17, n. 6, p. 926, doi. 10.1111/j.1365-2516.2011.02513.x
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Atherosclerotic heart disease: prevalence and risk factors in hospitalized men with haemophilia A.
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- Haemophilia, 2011, v. 17, n. 6, p. 867, doi. 10.1111/j.1365-2516.2011.02501.x
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Comparing bleed frequency and factor concentrate use between haemophilia A and B patients.
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- Haemophilia, 2011, v. 17, n. 6, p. 872, doi. 10.1111/j.1365-2516.2011.02506.x
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Assessment and management of pain in haemophilia patients.
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- Haemophilia, 2011, v. 17, n. 6, p. 839, doi. 10.1111/j.1365-2516.2011.02567.x
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Clinical severity of haemophilia A: does the classification of the 1950s still stand?
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- Haemophilia, 2011, v. 17, n. 6, p. 849, doi. 10.1111/j.1365-2516.2011.02539.x
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Scuba diving by patients with haemophilia: a few notes of precaution.
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- Haemophilia, 2011, v. 17, n. 6, p. e1007, doi. 10.1111/j.1365-2516.2011.02651.x
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von Willebrand factor/factor VIII concentrate (Humate-P) for management of elective surgery in adults and children with von Willebrand disease.
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- Haemophilia, 2011, v. 17, n. 6, p. 895, doi. 10.1111/j.1365-2516.2011.02534.x
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Factor VIII inhibitors: a 50-year perspective.
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- Haemophilia, 2011, v. 17, n. 6, p. 831, doi. 10.1111/j.1365-2516.2011.02568.x
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In-hospital rehabilitation after multiple joint procedures of the lower extremities in haemophilia patients: clinical guidelines for physical therapists.
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- Haemophilia, 2011, v. 17, n. 6, p. 971, doi. 10.1111/j.1365-2516.2011.02527.x
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Pharmacokinetics and safety of a 270 mcg kg<sup>−1</sup> dose of room temperature stable recombinant activated factor VII in patients with haemophilia.
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- Haemophilia, 2011, v. 17, n. 6, p. 860, doi. 10.1111/j.1365-2516.2011.02498.x
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Assessing the impact of age, race, ethnicity and inhibitor status on functional limitations of patients with severe and moderately severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 6, p. 884, doi. 10.1111/j.1365-2516.2011.02509.x
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- Article