Results 241 to 250 of about 1,017,222 (288)
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Replacement therapy for congenital Factor X deficiency
Transfusion, 1985We studied a young woman with severe (< 1%) congenital factor X deficiency during a 2‐year period in order to document the levels of factor X required to provide hemostasis for vaginal bleeding, epistaxis, and hemarthroses, as well as during surgery.
R D, Knight, C F, Barr, B M, Alving
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Acquired Factor X Deficiency and Amyloidosis
American Journal of Clinical Pathology, 1977A selective acquired Factor X deficiency is an unusual occurrence. Six cases of an acquired Factor X deficiency in association with amyloidosis have been reported. This paper describes two additional cases, suggesting that this relationship may be more than coincidental.
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Treatment of Amyloidosis Associated Factor X Deficiency
Thrombosis and Haemostasis, 1976SummaryThis is the tenth patient in thirteen years to be reported with the findings of an isolated factor X deficiency associated with primary amyloidosis. A favorable response to factor IX concentrate was manifested by temporary clinical and laboratory correction of her diathesis.
J A, Spero +3 more
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Factor X Deficiency and Systemic Amyloidosis
New England Journal of Medicine, 1977The association of an isolated acquired factor X (Stuart-factor) deficiency and systemic acquired amyloidosis has been sporadically reported over the last 15 years,1 , 2 and over two thirds of the ...
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Systemic Amyloidosis Associated With Factor X Deficiency
Acta Pathologica Japonica, 1984An autopsy case of amyloidosis associated with factor X deficiency is reported. The patient showed a markedly decreased level of factor X (9% normal) and an extremely shortened half‐life of intravenously infused factor X. Amyloid deposition was present in most of the visceral organs with special involvement of the liver and spleen.
H, Shibuya +4 more
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Factor X and its deficiency states
Haemophilia, 1997Summary. Factor X is one of the vitamin‐K‐dependent serine proteases. As a result of its position at the convergence of the intrinsic and extrinsic pathways of the clotting cascade, it plays a crucial role in blood coagulation. Factor X interacts with components of both pathways of coagulation, leading to its activation and the formation of the ...
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One Missense Mutation in the Factor X Gene Causing Factor X Deficiency—Factor X Kanazawa
International Journal of Hematology, 2001We investigated the molecular basis of factor X deficiency in a Japanese patient whose factor X activity and antigen level were 45% and 50% of normal control values, respectively. All exons and intron/exon junctions of the factor X gene were studied using a strategy combining polymerase chain reaction (PCR) amplification and nonradioactive single ...
E, Morishita +8 more
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A NEW VARIANT OF FACTOR X DEFICIENCY (FACTOR X ROMA).
Thrombosis and Haemostasis, 1987A 13 years-old-girl was admitted in our Hospital for a large muscle hematoma of left psoas. At age 3 she had a severe tonsillar bleeding following angina. Afterwards she suffered from easy bruisability and recurrent epistaxis. Prothrombin time (PT) was slightly prolonged (14.7 sec, control 12 sec, INR 1.5), while a more marked prolongation in aPTT was ...
V De Stefano +3 more
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Factor X Deficiency in Primary Amyloidosis
New England Journal of Medicine, 1979MANY patients with acquired factor X deficiency associated with primary amyloidosis have a severe bleeding disorder.1 2 3 4 A Because administered factor X is rapidly removed from circulation, conc...
P R, Greipp, R A, Kyle, E J, Bowie
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[Factor X deficiency and pregnancy].
Annales francaises d'anesthesie et de reanimation, 2002Factor X deficiency is one of the rarest inherited coagulation disorders. It is an autosomal recessive inherited disease. In its homozygous form factor X deficiency has an estimated prevalence of 1: 500,000. However in its heterozygous form it has an estimated frequency of 1: 500 to 1: 2000.
K, Rezig +3 more
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