Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12857/123915
Title: Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)
Authors: Girolami, Antonio 
Cosi, Elisabetta 
Santarossa, Claudia 
Ferrari, Silvia 
Girolami, Bruno 
Lombardi, Anna Maria 
Keywords: FX deficiency;atherosclerosis;bleeding;heterozygotes;venous thrombosis
Keywords Plus: FACTOR-VII DEFICIENCY;STUART CLOTTING DEFECT;HEMORRHAGIC STATE;MOLECULAR DEFECT;MUTATION;PADUA;GENE;ABNORMALITY;HEREDITARY;PHENOTYPE
Mesh headings: Factor X;Factor X Deficiency;Hemorrhage;Heterozygote;Mutation
Secondary Mesh headings: Female;Follow-Up Studies;History, 20th Century;History, 21st Century;Humans;Male;Prevalence
Issue Date: Dec-2016
Publisher: WILEY-BLACKWELL
Journal: European journal of haematology 
Abstract: 
The main objective of the study was to evaluate the incidence of bleeding manifestations in heterozygotes for FX deficiency vs. unaffected family members. Secondary objective was to compare the prevalence of arterial or venous diseases found in the two groups.
URI: http://hdl.handle.net/20.500.12857/123915
ISSN: 09024441
DOI: 10.1111/ejh.12767
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