The great advances in recent years in the treatment of haemophilia have produced far-reaching changes in the prognosis of haemophilia. This is mainly attrib-utable to the application of viral-inactivating pro-cesses to therapeutic concentrates of coagulant factors of human origin, and the availability of new recombinant products for the treatment of this disease. In addition, the new antiviral therapies for the treatment of acquired immune deficiency syn-drome and hepatitis C have enhanced life expectancy Summary. This paper provides an outline of the results obtained in a cross-sectional study conducted primarily with the aim of ascertaining orthopaedic complications in a group of young severe A and B haemophiliacs, the effects which these...
Este artículo está disponible en la página web de la revista: http://www.amjorthopedics.comHemophili...
We evaluated the long-term results of three total hip and nine total knee arthroplasties in nine hae...
Introduction: Defects in blood coagulation can be congenital or acquired. Haemophilia belongs to the...
Haemophilia A and B are hereditary haemorrhagic disorders characterised by deficiency or dysfunction...
The aim of this thesis is to evaluate and investigate the magnitude of the two major complications o...
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or deficiency o...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Data from the Italian Hemophilia Centres were collected to perform a retrospective survey of joint a...
Data from the Italian Hemophilia Centres were collected to perform a retrospective survey of joint a...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Haemophilia, outcome, quality of life, physical assessment, orthopaedic assessment 2 Haemophilia is ...
Introduction Patients having severe hemophilia (levels of deficient factor below 1%) frequently suff...
Patients with haemophilia who have developed inhibitors against factor VIII (FVIII) or factor IX pre...
Haemophilia is a rare genetic disorder, that results from various degrees of deficiency of coagulati...
Haemophilia A (FVIII deficiency), haemophilia B (FIX deficiency) and von Willebrands Disease (VWD) a...
Este artículo está disponible en la página web de la revista: http://www.amjorthopedics.comHemophili...
We evaluated the long-term results of three total hip and nine total knee arthroplasties in nine hae...
Introduction: Defects in blood coagulation can be congenital or acquired. Haemophilia belongs to the...
Haemophilia A and B are hereditary haemorrhagic disorders characterised by deficiency or dysfunction...
The aim of this thesis is to evaluate and investigate the magnitude of the two major complications o...
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or deficiency o...
In hemophilic patients, recurrent intra-articular bleeding results in hemophilic arthropathy. The fr...
Data from the Italian Hemophilia Centres were collected to perform a retrospective survey of joint a...
Data from the Italian Hemophilia Centres were collected to perform a retrospective survey of joint a...
Replacement of the congenitally deficient factor VIII or IX through plasma-derived or recombinant co...
Haemophilia, outcome, quality of life, physical assessment, orthopaedic assessment 2 Haemophilia is ...
Introduction Patients having severe hemophilia (levels of deficient factor below 1%) frequently suff...
Patients with haemophilia who have developed inhibitors against factor VIII (FVIII) or factor IX pre...
Haemophilia is a rare genetic disorder, that results from various degrees of deficiency of coagulati...
Haemophilia A (FVIII deficiency), haemophilia B (FIX deficiency) and von Willebrands Disease (VWD) a...
Este artículo está disponible en la página web de la revista: http://www.amjorthopedics.comHemophili...
We evaluated the long-term results of three total hip and nine total knee arthroplasties in nine hae...
Introduction: Defects in blood coagulation can be congenital or acquired. Haemophilia belongs to the...