sYNoPsIs Factor VIII activity and factor VIII related-or Willebrand-antigen were studied in 49 known carriers of haemophilia A and 31 normal women, and the data were analysed by four statisti-cal approaches. Sixteen per cent of normals and 18 % of carriers were misclassified, overlapping with the other group. Although the percentage of carriers detected is higher when taking into account the results of both biological and immunological factor VIII, it is lower than others recently reported, and the discrepan-cies between the results obtained are discussed. Haemophilia A is X-chromosome linked and is characterized by decreased plasma factor VIII (anti-haemophilic factor A) levels as measured by specific clotting assays. The detection of carr...
Fifty patients with haemophilia B, belonging to 29 kindreds, were investigated with a highly sensiti...
A wide range of factor VIII and IX levels is observed in heterozygous carriers of he-mophilia as wel...
The existence of two genetic variants (allotypes) of normal human factor IX is used for carrier dete...
Eight laboratories in six countries cooperated to clarify several issues concerning the phenotypes o...
Factor VIII (F.VIII) and von Willebrand factor (VWF):Ag data collected by eight laboratories on a to...
The efficacy of using promptly frozen plasma samples in the diagnosis of the carrier state for hemop...
Haemophilia B, an X-linked recessive bleeding disorder characterized by lack or deficiency of factor...
Sixty probable carriers of haemophilia from 25 families were studied by using coagulation phenotype ...
Antihaemophilic-factor-A-antibodies, which had spontaneously arisen in 2 patients, were used to deve...
CGA----TGA (Arg----Term) transitions in the factor VIII gene causing severe haemophilia A were detec...
Haemophilia A and B are X-linked disorders caused by impaired synthesis of coagulation factors VIII ...
Haemophilia is an inherited bleeding disorder characterized by a deficiency in coagulation factor VI...
In 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carri...
Haemophilia A is an X-linked, recessively inherited bleeding disorder of varying severity, which res...
SUMMARY: Deficient or defective coagulation factor VIII (FVIII) and von Willebrand factor (VWF) can ...
Fifty patients with haemophilia B, belonging to 29 kindreds, were investigated with a highly sensiti...
A wide range of factor VIII and IX levels is observed in heterozygous carriers of he-mophilia as wel...
The existence of two genetic variants (allotypes) of normal human factor IX is used for carrier dete...
Eight laboratories in six countries cooperated to clarify several issues concerning the phenotypes o...
Factor VIII (F.VIII) and von Willebrand factor (VWF):Ag data collected by eight laboratories on a to...
The efficacy of using promptly frozen plasma samples in the diagnosis of the carrier state for hemop...
Haemophilia B, an X-linked recessive bleeding disorder characterized by lack or deficiency of factor...
Sixty probable carriers of haemophilia from 25 families were studied by using coagulation phenotype ...
Antihaemophilic-factor-A-antibodies, which had spontaneously arisen in 2 patients, were used to deve...
CGA----TGA (Arg----Term) transitions in the factor VIII gene causing severe haemophilia A were detec...
Haemophilia A and B are X-linked disorders caused by impaired synthesis of coagulation factors VIII ...
Haemophilia is an inherited bleeding disorder characterized by a deficiency in coagulation factor VI...
In 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carri...
Haemophilia A is an X-linked, recessively inherited bleeding disorder of varying severity, which res...
SUMMARY: Deficient or defective coagulation factor VIII (FVIII) and von Willebrand factor (VWF) can ...
Fifty patients with haemophilia B, belonging to 29 kindreds, were investigated with a highly sensiti...
A wide range of factor VIII and IX levels is observed in heterozygous carriers of he-mophilia as wel...
The existence of two genetic variants (allotypes) of normal human factor IX is used for carrier dete...