Results 201 to 210 of about 22,513 (247)
Some of the next articles are maybe not open access.
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
openaire +2 more sources
The Lancet
Haemophilia A and B are congenital X-linked bleeding disorders resulting from deficiencies in clotting factors VIII (haemophilia A) and IX (haemophilia B). Patients with severe deficiency, defined as having less than 1% of normal plasma factor activivity, often have spontaneous bleeding within the first few years of life.
Pratima, Chowdary +3 more
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Haemophilia A and B are congenital X-linked bleeding disorders resulting from deficiencies in clotting factors VIII (haemophilia A) and IX (haemophilia B). Patients with severe deficiency, defined as having less than 1% of normal plasma factor activivity, often have spontaneous bleeding within the first few years of life.
Pratima, Chowdary +3 more
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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
openaire +2 more sources
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
Haemophilia, 2006
Summary. The primary aim of this study was to analyse the data on 2269 haemophilic patients in the Polish National Register of Inherited Bleeding Disorders – 1953 haemophilia A patients and 316 haemophilia B patients. Haemophilia A occurred in 1512 families, haemophilia B in 240 families. In the majority of haemophilia A and B cases severe haemophilia
J, Windyga +6 more
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Summary. The primary aim of this study was to analyse the data on 2269 haemophilic patients in the Polish National Register of Inherited Bleeding Disorders – 1953 haemophilia A patients and 316 haemophilia B patients. Haemophilia A occurred in 1512 families, haemophilia B in 240 families. In the majority of haemophilia A and B cases severe haemophilia
J, Windyga +6 more
openaire +2 more sources
Haemophilia, 2006
Summary. Men with haemophilia have not only the challenges of living with HIV and/or HCV infection and premature arthritis as complications of their disorder, but they also confront the other ails of ageing. These include genitourinary problems such as prostatic hypertrophy, prostatic cancer and renal stone disease, and arterial disease for which ...
Street, Alison M. +4 more
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Summary. Men with haemophilia have not only the challenges of living with HIV and/or HCV infection and premature arthritis as complications of their disorder, but they also confront the other ails of ageing. These include genitourinary problems such as prostatic hypertrophy, prostatic cancer and renal stone disease, and arterial disease for which ...
Street, Alison M. +4 more
openaire +2 more sources
Nursing Standard, 1999
Although the majority of adults and children with haemophilia are registered at designated specialist centres, many will come into contact with nurses who are unfamiliar with the condition. This article dispels common myths and misunderstandings about the condition which contribute to less than effective management.
A, Susman-Shaw, C, Harrington
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Although the majority of adults and children with haemophilia are registered at designated specialist centres, many will come into contact with nurses who are unfamiliar with the condition. This article dispels common myths and misunderstandings about the condition which contribute to less than effective management.
A, Susman-Shaw, C, Harrington
openaire +2 more sources