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Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers. [PDF]
Pak J Med Sci, 2017 Khan MTM +4 more
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Prophylaxis use among males with haemophilia B in the United States. [PDF]
Haemophilia, 2017 Ullman M +5 more
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Sustained high trough factor IX activity levels with continued use of rIX-FP in adult and paediatric patients with haemophilia B. [PDF]
Haemophilia, 2019 Gill JC, Roberts J, Li Y, Castaman G.
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High resolution melting for F9 gene mutation analysis in patients with haemophilia B. [PDF]
Blood Transfus, 2019 Salviato R +3 more
europepmc +1 more source
Six-year FIX-padua gene therapy in hemophilia B
Blood AdvancesWolfgang Miesbach, Roland Herzog
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Knowledge on the Haemophilia Care Among Healthcare Providers in Tanzania: A Multicenter Cross-Sectional Study. [PDF]
J Blood MedRwezaula SS +5 more
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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
Thrombosis and Haemostasis, 1972
SummaryVariants of haemophilia B were examined by antibody-neutralization technique and by the ox brain thromboplastin time method. On the basis of the presence or absence of anomalous factor IX and of prothrombin time, four variants of haemophilia B were discerned. It is shown that the prolongation of prothrombin time, measured in our cases, cannot be
S, Elödi, E, Puskás
openaire +2 more sources
SummaryVariants of haemophilia B were examined by antibody-neutralization technique and by the ox brain thromboplastin time method. On the basis of the presence or absence of anomalous factor IX and of prothrombin time, four variants of haemophilia B were discerned. It is shown that the prolongation of prothrombin time, measured in our cases, cannot be
S, Elödi, E, Puskás
openaire +2 more sources
Thrombosis and Haemostasis, 1962
SummaryA 6 year old girl with symptoms of severe haemophilia and a haemophilia B factor B content of 2%—3% of normal is described. Investigation of the family revealed that the mother and the sister of the girl were carriers of the haemophilia B gene, while the father was normal. Chromosome studies showed a pattern of 2 X chromosomes.
J E, NILEHN, I M, NILSSON
openaire +2 more sources
SummaryA 6 year old girl with symptoms of severe haemophilia and a haemophilia B factor B content of 2%—3% of normal is described. Investigation of the family revealed that the mother and the sister of the girl were carriers of the haemophilia B gene, while the father was normal. Chromosome studies showed a pattern of 2 X chromosomes.
J E, NILEHN, I M, NILSSON
openaire +2 more sources