Results 301 to 310 of about 1,584,900 (350)
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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 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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Amyloidosis with factor X deficiency
THE AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1972B, Bernhardt +3 more
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Factor II, Factor V and Factor X Deficiencies
2009Inherited deficiencies of factors II, V and X (FII, FV, FX) are rare (estimated frequencies are: FII, 1 in 2,000,000; FV, 1 in 1,000,000; and FX, 1 in 500,000). Patients who are homozygous or compound heterozygous for defects in the FII, FV or FX genes can have moderate to severe bleeding symptoms, with patients having FX deficiency more likely to ...
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Factor X Deficiency in Primary Amyloidosis
New England Journal of Medicine, 1980R P, Fogdall, D P, Fischbach
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Factor‐X deficiency in amyloidosis: A critical review
American journal of hematology/oncology, 1981P. Greipp, R. Kyle, E. Bowie
semanticscholar +1 more source
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Nature Medicine, 2021Masato Ogishi, Rui Yang, Caner Aytekin
exaly

