What's the difference between haemophilia and hemophilia?
Haemophilia
Definition:
Example Sentences:
Hemophilia
Definition:
(n.) See Hematophilia.
Example Sentences:
(1) It proved successful in various hemorrhagic disorders mild forms of hemophilia A.
(2) Hemophilia type A or B is due to deficiency in factor VIII C or IX C, but whatever the type and whether the affection is severe or attenuated the risk of hemorrhage after surgery is identical.
(3) Women who were the mothers of individuals with isolated cases of hemophilia appeared to be carriers in at least 85% of cases, suggesting that the frequency of cases due to fresh mutations is low.
(4) At that time the factor IX users also had milder immune aberrations than the hemophilia A group.
(5) This confirms the effectively of high-dose immunoglobulin therapy for hemophilia, due to acquired factor VIII antibodies, also in patients with severe SLE.
(6) The associated of hemophilia and transposition, observed also by others, is extremely unlikely by chance and suggests genetic errors of endothelial cell function.
(7) Twelve patients with classic hemophilia were studied.
(8) In the U.S. and Europe, AIDS correlates to 95% with risk factors, such as about 8 years of promiscuous male homosexuality, intravenous drug use, or hemophilia.
(9) Consequently, to intensify the procoagulant activity without changes in fibrinolysis (for example hemophilia) it is necessary to use the vasopressin injection in combination with atropine.
(10) These results provide the rationale for using skeletal myoblasts as an efficient gene delivery vehicle in the somatic gene therapy for hemophilia B.
(11) Assessment of factor IX antigen and factor IX coagulant activity has confirmed the genetic heterogeneity of hemophilia B and has shown that some affected patients have normal amounts of factor IX-like protein.
(12) Concanavalin A (Con-A)-induced suppression of T cell proliferation was studied in 48 patients with severe hemophilia.
(13) Hence, first-trimester prenatal diagnosis of hemophilia A is feasible for the great majority of fetuses at risk through combined use of all the available intragenic and extragenic probes, providing key family members are available.
(14) Bleeding episodes in patients with hemophilia A with anti-factor VII antibodies are frequently difficult to treat.
(15) Furthermore, the authors report on the complications and treatment in special cases; i. e., patients with horseshoe kidneys, solitary kidneys, spinal cord lesions, radiolucent calculi, hemophilia, and staghorn stones.
(16) Major areas of knowledge deficiency included knowledge about how one contracts hemophilia and the purpose of treatment.
(17) Twenty-six unrelated hemophilia A and 70 unrelated normal chromosomes in 184 subjects were studied to determine the frequencies of intragenic and intergenic restriction fragment length polymorphisms associated with the factor VIII:C gene.
(18) A 28-year-old white male with classic hemophilia A sustained a 30.5% total body surface area burn.
(19) The 95 per cent confidence interval for the probability of a recombination between St14 and hemophilia A is 0 to 6.5 per cent.
(20) Specifically, although aware of the importance of using condoms, sexually active adolescents with hemophilia were not practicing safe sex.