Results 241 to 250 of about 32,062 (289)
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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
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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
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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
International Journal of Sports Medicine, 2011
One of the most important objectives of intervention programs for persons with haemophilia (PWH) is to improve their quality of life. Regular physical activity has been recommended as an adjunct to conventional treatment, with positive results in the prevention of joint problems and bleeding, in addition to the improvement in cardiovascular function ...
J C, Souza +5 more
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One of the most important objectives of intervention programs for persons with haemophilia (PWH) is to improve their quality of life. Regular physical activity has been recommended as an adjunct to conventional treatment, with positive results in the prevention of joint problems and bleeding, in addition to the improvement in cardiovascular function ...
J C, Souza +5 more
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Optimizing factor prophylaxis for the haemophilia population: where do we stand?
Haemophilia, 2004 The hallmark of severe haemophilia, defined as a circulating level of factor (F) VIII (haemophilia A cases) or FIX (haemophilia B cases) of < 1%, is recurrent bleeding into muscles and joints (haemarthroses) from an early age of life.
Rolf C R Ljung +2 more
exaly +2 more sources
Chondrocalcinosis and haemophilia
Clinical Radiology, 1977Chondrocalcinosis has been found in a wide variety of diseases. Cartilage calcification is commonly noted in patients with haemochromatosis, but it has not been previously reported in haemophilia, although increased levels of iron are present in the joints in both these conditions.
P S, Jensen, C E, Putman
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British Journal of Haematology, 1993
In the present study DNA from 281 unrelated haemophilia A patients including 15 inhibitor patients has been analysed by Southern blotting technique. Using various restriction enzymes, cloned factor VIII cDNA probes and genomic fragments we have identified 14 mutations. Six of the mutations are novel partial factor VIII gene deletions.
R, Schwaab +4 more
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In the present study DNA from 281 unrelated haemophilia A patients including 15 inhibitor patients has been analysed by Southern blotting technique. Using various restriction enzymes, cloned factor VIII cDNA probes and genomic fragments we have identified 14 mutations. Six of the mutations are novel partial factor VIII gene deletions.
R, Schwaab +4 more
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Haemophilia, 2007
Summary. Haemophilia, an ancient disease, now has sophisticated methods for diagnosis and treatment. The genetically missing factors can now be supplied by fractionation of human‐derived (HD) plasma or with recombinant technology (r). Making therapeutic choices is complicated by past transfusion‐transmitted diseases. HD and r products now have similar
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Summary. Haemophilia, an ancient disease, now has sophisticated methods for diagnosis and treatment. The genetically missing factors can now be supplied by fractionation of human‐derived (HD) plasma or with recombinant technology (r). Making therapeutic choices is complicated by past transfusion‐transmitted diseases. HD and r products now have similar
openaire +2 more sources
Transactions of the Royal Society of Tropical Medicine and Hygiene, 1968
Abstract 8 patients with haemophilia, with 11 affected relatives, are reported in Uganda Africans. Reasons are given for believing that haemophilia may be no rarer in Africans than in other peoples.
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Abstract 8 patients with haemophilia, with 11 affected relatives, are reported in Uganda Africans. Reasons are given for believing that haemophilia may be no rarer in Africans than in other peoples.
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Haemostasis, 2009
As first step for the development of a programme of haemophilia care, the disease was diagnosed locally in 5 bleeders. These patients were all affected by severe haemophilia A. They were treated with fresh frozen plasma for bleedings. All of them were negative for antibodies to HIV.
O A, Abdulle +5 more
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As first step for the development of a programme of haemophilia care, the disease was diagnosed locally in 5 bleeders. These patients were all affected by severe haemophilia A. They were treated with fresh frozen plasma for bleedings. All of them were negative for antibodies to HIV.
O A, Abdulle +5 more
openaire +2 more sources