Works matching IS 13518216 AND DT 2010 AND VI 16 AND IP 4
Results: 25
A review of long-term prophylaxis in the rare inherited coagulation factor deficiencies.
- Published in:
- Haemophilia, 2010, v. 16, n. 4, p. 569, doi. 10.1111/j.1365-2516.2009.02118.x
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- Publication type:
- Article
Bernard Soulier syndrome in pregnancy: a systematic review.
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- Haemophilia, 2010, v. 16, n. 4, p. 584, doi. 10.1111/j.1365-2516.2009.02137.x
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- Publication type:
- Article
How we treat: Haematuria in adults with haemophilia.
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- Haemophilia, 2010, v. 16, n. 4, p. 683, doi. 10.1111/j.1365-2516.2009.02171.x
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- Article
Laboratory identification of factor VIII inhibitors in the real world: the experience from Australasia.
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- Haemophilia, 2010, v. 16, n. 4, p. 662, doi. 10.1111/j.1365-2516.2009.02173.x
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- Publication type:
- Article
Knowledge of disease and adherence in adult patients with haemophilia.
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- Haemophilia, 2010, v. 16, n. 4, p. 592, doi. 10.1111/j.1365-2516.2009.02189.x
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- Publication type:
- Article
Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancy.
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- Haemophilia, 2010, v. 16, n. 4, p. 671, doi. 10.1111/j.1365-2516.2009.02190.x
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- Publication type:
- Article
Limited blood sampling for pharmacokinetic dose tailoring of FVIII in the prophylactic treatment of haemophilia A.
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- Haemophilia, 2010, v. 16, n. 4, p. 597, doi. 10.1111/j.1365-2516.2009.02191.x
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- Publication type:
- Article
Radioisotope synoviorthesis with Holmium-166-chitosan complex in haemophilic arthropathy.
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- Haemophilia, 2010, v. 16, n. 4, p. 640, doi. 10.1111/j.1365-2516.2009.02192.x
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- Publication type:
- Article
Balance dysfunction in adults with haemophilia.
- Published in:
- Haemophilia, 2010, v. 16, n. 4, p. 606, doi. 10.1111/j.1365-2516.2010.02200.x
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- Article
Pseudoaneurysm in association with a knee endoprothesis operation in an inhibitor-positive haemophilia A patient – treatment with local thrombin.
- Published in:
- 2010
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- Publication type:
- Letter
Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE<sup>®</sup> in patients with von Willebrand’s disease: a prospective multi-centre study.
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- Haemophilia, 2010, v. 16, n. 4, p. 615, doi. 10.1111/j.1365-2516.2010.02206.x
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- Publication type:
- Article
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency.
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- Haemophilia, 2010, v. 16, n. 4, p. 675, doi. 10.1111/j.1365-2516.2010.02207.x
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- Publication type:
- Article
Recombinant activated factor VII safety and efficacy in the treatment of cranial haemorrhage in patients with congenital haemophilia with inhibitors: an analysis of the Hemophilia and Thrombosis Research Society Registry (2004–2008).
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- Haemophilia, 2010, v. 16, n. 4, p. 625, doi. 10.1111/j.1365-2516.2010.02208.x
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- Publication type:
- Article
Haemothorax in children with congenital coagulopathy.
- Published in:
- 2010
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- Publication type:
- Letter
The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A.
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- Haemophilia, 2010, v. 16, n. 4, p. 632, doi. 10.1111/j.1365-2516.2010.02211.x
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- Publication type:
- Article
Acute myocardial infarction in a Chinese patient with haemophilia A and risk factors for coronary artery disease: a case report with autopsy.
- Published in:
- 2010
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- Publication type:
- Letter
Molecular basis of factor X deficiency cases from India.
- Published in:
- 2010
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- Publication type:
- Letter
Assessing baseline joint hypermobility as a risk factor for arthropathy development in moderate and severe haemophilia.
- Published in:
- 2010
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- Publication type:
- Letter
Psychosocial correlates of physical activity in adolescents with haemophilia.
- Published in:
- Haemophilia, 2010, v. 16, n. 4, p. 656, doi. 10.1111/j.1365-2516.2010.02217.x
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- Publication type:
- Article
Thrombin time and fibrinogen as initial screening tests for people with inherited bleeding disorders.
- Published in:
- 2010
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- Publication type:
- Letter
Haemophilic arthropathy of the ankle treated by total ankle replacement: a case series.
- Published in:
- Haemophilia, 2010, v. 16, n. 4, p. 647, doi. 10.1111/j.1365-2516.2010.02221.x
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- Publication type:
- Article
Factor VIII/von Willebrand factor concentrate for treatment of life threatening epistaxis in Glanzmann’s thrombasthenia.
- Published in:
- 2010
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- Publication type:
- Letter
Peri-interventional control of haemostasis in a patient with combined coagulation factor V- and factor VIII-deficiency and anaphylaxis to fresh frozen plasma – a rare indication for recombinant factor VIIa.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Treatment of mantle cell lymphoma with autologous stem-cell transplantation in a patient with severe congenital haemophilia-A and chronic (B and C virus) hepatitis.
- Published in:
- 2010
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- Publication type:
- Letter
Control of variceal bleeding in a patient with severe haemophilia A and factor VIII inhibitors using a transjugular intrahepatic portosystemic shunt.
- Published in:
- 2010
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- Publication type:
- Letter