Works matching IS 13518216 AND DT 2011 AND VI 17 AND IP 3
Results: 36
Low incidence of factor VIII inhibitors in previously untreated patients during prophylaxis, on-demand treatment and surgical procedures, with Octanate.
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- Haemophilia, 2011, v. 17, n. 3, p. 399, doi. 10.1111/j.1365-2516.2010.02428.x
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- Article
Elective surgery in patients with congenital coagulopathies and inhibitors: experience of the National Haemophilia Centre of Venezuela.
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- Haemophilia, 2011, v. 17, n. 3, p. 422, doi. 10.1111/j.1365-2516.2010.02427.x
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- Article
Low risk of inhibitor formation in haemophilia A patients following en masse switch in treatment to a third generation full length plasma and albumin-free recombinant factor VIII product (ADVATE.
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- Haemophilia, 2011, v. 17, n. 3, p. 407, doi. 10.1111/j.1365-2516.2010.02430.x
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- Article
The clinical efficacy and safety of the FVIII/VWF concentrate, BIOSTATE.
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- Haemophilia, 2011, v. 17, n. 3, p. 463, doi. 10.1111/j.1365-2516.2010.02445.x
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- Article
Bone mineral density in Iranian patients with haemophilia: the first experience in southern Iran.
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- Haemophilia, 2011, v. 17, n. 3, p. 552, doi. 10.1111/j.1365-2516.2010.02416.x
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- Article
Massive retroperitoneal haemorrhage in a neonate with severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 3, p. 547, doi. 10.1111/j.1365-2516.2010.02409.x
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- Article
Abstracts of the Hemostasis & Thrombosis Research Society, 2011 Annual Scientific Symposium, April 28-30, Northwestern Memorial Hospital, Chicago, IL.
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- 2011
- Publication type:
- Abstract
The perspective of patients with haemophilia with inhibitors and their care givers: preferences for treatment characteristics.
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- Haemophilia, 2011, v. 17, n. 3, p. 476, doi. 10.1111/j.1365-2516.2010.02401.x
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- Article
Experience with Optivate.
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- Haemophilia, 2011, v. 17, n. 3, p. 428, doi. 10.1111/j.1365-2516.2010.02441.x
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- Article
Focusing on haemophilia B: prophylaxis in Spanish patients.
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- Haemophilia, 2011, v. 17, n. 3, p. 542, doi. 10.1111/j.1365-2516.2010.02412.x
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- Article
Application of UKHCDO 2004 guidelines in type 1 von Willebrand Disease - a single centre paediatric experience of the implications of altered or removed diagnosis.
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- Haemophilia, 2011, v. 17, n. 3, p. 522, doi. 10.1111/j.1365-2516.2010.02452.x
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- Article
Arterial pseudoaneurysms in haemophilia: conservative treatment with observation and factor replacement.
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- Haemophilia, 2011, v. 17, n. 3, p. 550, doi. 10.1111/j.1365-2516.2010.02434.x
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- Article
Acquired factor XIII inhibitor: clinical features, treatment, fibrin structure and epitope determination.
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- Haemophilia, 2011, v. 17, n. 3, p. 393, doi. 10.1111/j.1365-2516.2010.02459.x
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- Article
Management of acute haemarthrosis in haemophilia A without inhibitors: literature review, European survey and recommendations.
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- Haemophilia, 2011, v. 17, n. 3, p. 383, doi. 10.1111/j.1365-2516.2010.02449.x
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- Article
Abstracts of the HTRS/NASCOLA Scientific Symposium, April 15-17, 2010 Northwestern Memorial Hospital, Chicago, Illinois, Poster Presentations - Categories: Young Investigators, Senior Investigators, Information of Interest.
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- Haemophilia, 2011, v. 17, n. 3, p. 558, doi. 10.1111/j.1365-2516.2011.02550.x
- Publication type:
- Article
Successful treatment of an injury bleeding on a patient suffering from mild von Willebrand's disease and predisposition to allergic diseases, with recombinant factor VIIA.
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- Haemophilia, 2011, v. 17, n. 3, p. 545, doi. 10.1111/j.1365-2516.2010.02410.x
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- Article
A consensus statement on clinical trials of bypassing agent prophylaxis in inhibitor patients.
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- Haemophilia, 2011, v. 17, n. 3, p. 516, doi. 10.1111/j.1365-2516.2010.02440.x
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- Article
Standardization of thromboelastography: a report from the TEG-ROTEM working group.
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- Haemophilia, 2011, v. 17, n. 3, p. 532, doi. 10.1111/j.1365-2516.2010.02451.x
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- Article
Body structure versus body function in haemophilia: the case of haemophilic ankle arthropathy.
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- Haemophilia, 2011, v. 17, n. 3, p. 508, doi. 10.1111/j.1365-2516.2010.02433.x
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- Article
Prevalence of the factor 8 gene intron 1 inversion in Chinese haemophiliacs and its application to carrier detection and prenatal diagnosis in haemophilia A families.
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- Haemophilia, 2011, v. 17, n. 3, p. 541, doi. 10.1111/j.1365-2516.2010.02444.x
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- Article
'Just an unfortunate coincidence': children's understanding of haemophilia genetics and inheritance.
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- Haemophilia, 2011, v. 17, n. 3, p. 470, doi. 10.1111/j.1365-2516.2010.02448.x
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- Article
A study of reported factor IX use around the world.
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- Haemophilia, 2011, v. 17, n. 3, p. 446, doi. 10.1111/j.1365-2516.2010.02461.x
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- Article
Immune tolerance induction in 31 children with haemophilia A: is ITI less successful in African Americans?
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- Haemophilia, 2011, v. 17, n. 3, p. 483, doi. 10.1111/j.1365-2516.2010.02429.x
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- Article
Trends in bleeding patterns during prophylaxis for severe haemophilia: observations from a series of prospective clinical trials.
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- Haemophilia, 2011, v. 17, n. 3, p. 433, doi. 10.1111/j.1365-2516.2010.02450.x
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- Article
Six-month clinical observation on safety and efficacy of a full-length recombinant factor VIII for on-demand treatment of Chinese patients with haemophilia A.
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- Haemophilia, 2011, v. 17, n. 3, p. 538, doi. 10.1111/j.1365-2516.2010.02432.x
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- Article
Oral health in adult patients with congenital coagulation disorders - a case control study.
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- Haemophilia, 2011, v. 17, n. 3, p. 527, doi. 10.1111/j.1365-2516.2010.02443.x
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- Article
Surgical treatment of arteriovenous fistula and brachial artery aneurysm in a patient with mild haemophilia A.
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- Haemophilia, 2011, v. 17, n. 3, p. 548, doi. 10.1111/j.1365-2516.2010.02425.x
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- Article
A retrospective study to describe the incidence of moderate to severe allergic reactions to factor IX in subjects with haemophilia B.
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- Haemophilia, 2011, v. 17, n. 3, p. 494, doi. 10.1111/j.1365-2516.2011.02436.x
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- Article
Identification of novel and recurrent mutations in Tunisian haemophilia B patients.
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- Haemophilia, 2011, v. 17, n. 3, p. 544, doi. 10.1111/j.1365-2516.2010.02442.x
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- Article
Persistent factor VIII inhibitors and orthopaedic complications in children with severe haemophilia A.
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- Haemophilia, 2011, v. 17, n. 3, p. 490, doi. 10.1111/j.1365-2516.2010.02447.x
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- Article
Dengue virus infection in haemophilic patients: aggravation of bleeding risk.
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- Haemophilia, 2011, v. 17, n. 3, p. 553, doi. 10.1111/j.1365-2516.2010.02413.x
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- Article
Range of motion measurements: reference values and a database for comparison studies.
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- Haemophilia, 2011, v. 17, n. 3, p. 500, doi. 10.1111/j.1365-2516.2010.02399.x
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- Article
An ultrapure plasma-derived monoclonal antibody-purified factor IX concentrate (Nonafact.
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- Haemophilia, 2011, v. 17, n. 3, p. 439, doi. 10.1111/j.1365-2516.2010.02453.x
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- Article
The relative burden of haemophilia A and the impact of target joint development on health-related quality of life: results from the ADVATE Post-Authorization Safety Surveillance (PASS) study.
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- Haemophilia, 2011, v. 17, n. 3, p. 412, doi. 10.1111/j.1365-2516.2010.02435.x
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- Article
Abstracts of the HTRS/NASCOLA Scientific Symposium, April 15-17, 2010, Chicago, IL - Category: 2010 Travel Award Winners.
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- Haemophilia, 2011, v. 17, n. 3, p. 556, doi. 10.1111/j.1365-2516.2011.02549.x
- Publication type:
- Article
Clinical assessment of Optivate.
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- Haemophilia, 2011, v. 17, n. 3, p. 456, doi. 10.1111/j.1365-2516.2010.02446.x
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- Publication type:
- Article