Works matching IS 13518216 AND DT 2012 AND VI 18 AND IP 4
Results: 37
A comparison of traditional vs. Canadian tailored prophylaxis dosing of prophylactic factor infusions in children with haemophilia A and B in a single hemophilia treatment center.
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- Haemophilia, 2012, v. 18, n. 4, p. 561, doi. 10.1111/j.1365-2516.2011.02741.x
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Learning intravenous infusion in haemophilia: experience from the Netherlands.
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- Haemophilia, 2012, v. 18, n. 4, p. 516, doi. 10.1111/j.1365-2516.2012.02752.x
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A case of acquired FXIII deficiency with severe bleeding symptoms.
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- Haemophilia, 2012, v. 18, n. 4, p. 618, doi. 10.1111/j.1365-2516.2012.02763.x
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Access to primary dental care for patients with inherited bleeding disorders.
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- Haemophilia, 2012, v. 18, n. 4, p. 510, doi. 10.1111/j.1365-2516.2011.02716.x
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Accurate tracking genetic markers in haemophilia linkage analysis: a matter beyond scientific priority.
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- Haemophilia, 2012, v. 18, n. 4, p. e359, doi. 10.1111/j.1365-2516.2012.02859.x
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Development and introduction of recombinant factor VIII - a clinician's experience.
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- Haemophilia, 2012, v. 18, n. 4, p. 483, doi. 10.1111/j.1365-2516.2012.02804.x
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Comment on: Forde K, Mason C, Mathias M. Prolonged bleeding after exfoliation of a deciduous tooth in a patient with Glanzmann's thrombasthenia. Haemophilia 2012; 18: e58-59.
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- Haemophilia, 2012, v. 18, n. 4, p. e347, doi. 10.1111/j.1365-2516.2012.02844.x
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A complex case of infected total knee arthroplasty in a haemophilic patient with inhibitor.
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- Haemophilia, 2012, v. 18, n. 4, p. e357, doi. 10.1111/j.1365-2516.2012.02815.x
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Current prescription of prophylactic factor infusions and perceived adherence for children and adolescents with haemophilia: a survey of haemophilia healthcare professionals in the United States.
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- Haemophilia, 2012, v. 18, n. 4, p. 568, doi. 10.1111/j.1365-2516.2012.02756.x
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Iatrogenic fracture of the proximal tibia as a complication of knee manipulation under anaesthesia in a haemophilia patient with an ipsilateral stiff knee secondary to a supracondylar non-union of the femur.
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- Haemophilia, 2012, v. 18, n. 4, p. e354, doi. 10.1111/j.1365-2516.2012.02814.x
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Identical but different: haemophilia B in monozygotic twins with inhibitor in one brother and subsequent successful immune tolerance induction.
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- Haemophilia, 2012, v. 18, n. 4, p. e349, doi. 10.1111/j.1365-2516.2012.02865.x
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Patient- and caregiver-reported bleeding symptoms and reasons for starting and stopping treatment with recombinant factor VIIa: analysis of the Dosing Observational Study in Haemophilia (DOSE).
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- Haemophilia, 2012, v. 18, n. 4, p. 554, doi. 10.1111/j.1365-2516.2012.02762.x
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Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom.
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- Haemophilia, 2012, v. 18, n. 4, p. 575, doi. 10.1111/j.1365-2516.2011.02653.x
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The PFA-100<sup>®</sup> does not predict delta-granule platelet storage pool deficiencies.
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- Haemophilia, 2012, v. 18, n. 4, p. 626, doi. 10.1111/j.1365-2516.2011.02733.x
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Interim data on long-term efficacy, safety and tolerability of a plasma-derived factor VIII concentrate in 109 patients with severe haemophilia A.
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- Haemophilia, 2012, v. 18, n. 4, p. 496, doi. 10.1111/j.1365-2516.2011.02738.x
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Why don't haemophilia nurses do research?
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- Haemophilia, 2012, v. 18, n. 4, p. 540, doi. 10.1111/j.1365-2516.2012.02749.x
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Acquired haemophilia in a patient with castleman's disease: a case report.
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- Haemophilia, 2012, v. 18, n. 4, p. e360, doi. 10.1111/j.1365-2516.2012.02850.x
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Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disorders.
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- Haemophilia, 2012, v. 18, n. 4, p. 630, doi. 10.1111/j.1365-2516.2012.02759.x
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A strategy for carrier detection in Pakistani haemophilia B families.
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- Haemophilia, 2012, v. 18, n. 4, p. e348, doi. 10.1111/j.1365-2516.2012.02860.x
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Incremental cost effectiveness analysis for Haemophilia Home-Based Care Programme in Thailand.
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- Haemophilia, 2012, v. 18, n. 4, p. e362, doi. 10.1111/j.1365-2516.2012.02871.x
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Assessment of von Willebrand disease as a risk factor for primary postpartum haemorrhage.
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- Haemophilia, 2012, v. 18, n. 4, p. 593, doi. 10.1111/j.1365-2516.2012.02750.x
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How we treat: considerations for physiotherapy in the patient with haemophilia and inhibitors undergoing elective orthopaedic surgery.
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- Haemophilia, 2012, v. 18, n. 4, p. 550, doi. 10.1111/j.1365-2516.2012.02755.x
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Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees.
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- Haemophilia, 2012, v. 18, n. 4, p. 621, doi. 10.1111/j.1365-2516.2011.02732.x
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Use of acupuncture in the management of chronic haemophilia pain.
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- Haemophilia, 2012, v. 18, n. 4, p. 613, doi. 10.1111/j.1365-2516.2012.02766.x
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Combined treatment with APCC (FEIBA<sup>®</sup>) and tranexamic acid in patients with haemophilia A with inhibitors and in patients with acquired haemophilia A - a two-centre experience.
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- Haemophilia, 2012, v. 18, n. 4, p. 544, doi. 10.1111/j.1365-2516.2012.02748.x
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MRI after removal of central venous access device reveals a high number of asymptomatic thromboses in children with haemophilia.
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- Haemophilia, 2012, v. 18, n. 4, p. 521, doi. 10.1111/j.1365-2516.2011.02719.x
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The UK Haemophilia Doctors Organisation triennial audit of UK Comprehensive Care Haemophilia Centres.
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- Haemophilia, 2012, v. 18, n. 4, p. 491, doi. 10.1111/j.1365-2516.2012.02817.x
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A prospective registry of European haemophilia B patients receiving nonacog alfa, recombinant human factor IX, for usual use.
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- Haemophilia, 2012, v. 18, n. 4, p. 503, doi. 10.1111/j.1365-2516.2011.02685.x
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6th Congress of the European Association for Haemophilia and Allied Disorders (EAHAD) 6-8 February 2013, Warsaw, Poland.
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- Haemophilia, 2012, v. 18, n. 4, p. 647, doi. 10.1111/j.1365-2516.2012.02868.x
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- Article
Quality of life in adult patients with haemophilia - a single centre experience from Sweden.
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- Haemophilia, 2012, v. 18, n. 4, p. 527, doi. 10.1111/j.1365-2516.2012.02765.x
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Intravascular recovery of VWF and FVIII following intraperitoneal injection and differences from intravenous and subcutaneous injection in mice.
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- Haemophilia, 2012, v. 18, n. 4, p. 639, doi. 10.1111/j.1365-2516.2011.02735.x
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Management of muscle haematomas in patients with severe haemophilia in an evidence-poor world.
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- Haemophilia, 2012, v. 18, n. 4, p. 598, doi. 10.1111/j.1365-2516.2011.02720.x
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Surgical wound healing in bleeding disorders.
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- Haemophilia, 2012, v. 18, n. 4, p. 487, doi. 10.1111/j.1365-2516.2012.02760.x
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Prevalence of malignancies among U.S. male patients with haemophilia: a review of the Haemophilia Surveillance System.
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- Haemophilia, 2012, v. 18, n. 4, p. 532, doi. 10.1111/j.1365-2516.2011.02731.x
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Prenatal diagnosis for haemophilia: a nationwide survey among female carriers in the Netherlands.
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- Haemophilia, 2012, v. 18, n. 4, p. 584, doi. 10.1111/j.1365-2516.2011.02742.x
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Short and long-term management of haemophilia A patient requiring heart valve surgery.
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- Haemophilia, 2012, v. 18, n. 4, p. e352, doi. 10.1111/j.1365-2516.2012.02812.x
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Perioperative clotting factor replacement and infection in total knee arthroplasty.
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- Haemophilia, 2012, v. 18, n. 4, p. 607, doi. 10.1111/j.1365-2516.2011.02728.x
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- Article