Results 191 to 200 of about 22,513 (247)
Quantitative and qualitative motion analysis for early detection of joint damage in haemophilia patients: study protocol for a pilot feasibility study at a German haemophilia treatment centre. [PDF]
BMJ OpenSchober S, Hansmann S.
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Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten-Year Single-Centre Experience. [PDF]
HaemophiliaMortarino M +6 more
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Accuracy of Factor VIII Assays for Measuring Damoctocog Alfa Pegol: A Comparative Analysis. [PDF]
HaemophiliaCluitmans JCA +3 more
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Nonneutralizing Antibodies in Haemophilia A Patients: To Be Ignored or Not to Be! [PDF]
HaemophiliaShetty S +8 more
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Integrating Clinical, Functional, and Patient-Reported Outcomes in Haemophilia Care: A Delphi-Based Consensus on a New Monitoring Tool. [PDF]
J Clin MedMolinari AC +18 more
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Nature Reviews Disease Primers, 2021
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease depends on the reduction of levels of FVIII or FIX, which are determined by the type of the causative mutation in the genes encoding the factors (F8 and F9 ...
Erik Berntorp +6 more
openaire +2 more sources
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease depends on the reduction of levels of FVIII or FIX, which are determined by the type of the causative mutation in the genes encoding the factors (F8 and F9 ...
Erik Berntorp +6 more
openaire +2 more sources
British Journal of Perioperative Nursing (United Kingdom), 2004
This is the third article in a series that aims to refresh readers’ knowledge of blood. This article describes haemophilia which is a congenital disorder of coagulation. Vicky Vidler describes the aetiology of Haemophilia A and B, their clinical manifestations and the treatment options available to manage these patients in the perioperative period.
Vicky Vidler, Falicia Cox
openaire +2 more sources
This is the third article in a series that aims to refresh readers’ knowledge of blood. This article describes haemophilia which is a congenital disorder of coagulation. Vicky Vidler describes the aetiology of Haemophilia A and B, their clinical manifestations and the treatment options available to manage these patients in the perioperative period.
Vicky Vidler, Falicia Cox
openaire +2 more sources
Lancet, The, 2003
The haemophilias are inherited disorders in which one of the coagulation factors is deficient. Although deficiencies of factor VIII (haemophilia A) and factor IX (haemophilia B) are well recognised, von Willebrand's disease is much more common. Rare defects can occur in any of the coagulation factors.
K John Pasi
exaly +3 more sources
The haemophilias are inherited disorders in which one of the coagulation factors is deficient. Although deficiencies of factor VIII (haemophilia A) and factor IX (haemophilia B) are well recognised, von Willebrand's disease is much more common. Rare defects can occur in any of the coagulation factors.
K John Pasi
exaly +3 more sources