Results 21 to 30 of about 23,458 (249)
Clinical Case Reports, 2022 Factor VII and XI deficiencies are rare bleeding disorders typically associated with mild or provoked bleeding. This case report describes a patient with factor VII and XI deficiencies with an unprovoked episode of lower extremity hematoma causing ...
Joseph P. Marshalek +3 more
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Coronary artery stenting in a patient with factor XI deficiency
Cardiology Plus, 2019 Factor XI deficiency is a rare coagulopathy which has a higher risk of bleeding following trauma or an operation. Stable coronary artery disease patients complicated by factor XI deficiency draw extraordinary caution when coronary artery stents are ...
Mingqiang Fu +4 more
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Haemophilia, 2008 Summary. Although factor XI (FXI) deficiency has a particularly high incidence in Ashkenazi Jews, it is now frequently diagnosed in other ethnic groups. This review gives an overview of the basic pathophysiology, clinical manifestations, and management of FXI deficiency.
K, Gomez, P, Bolton-Maggs
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Perioperative care of an adolescent with factor XI deficiency during posterior spinal fusion. [PDF]
Pediatric Anesthesia and Critical Care Journal (PACCJ)Factor XI (FXI) deficiency (Rosenthal disease or hemo- philia C) is a uncommon autosomal recessive bleeding disorder. Clinical signs and symptoms of factor XI de- ficiency are generally limited; however, significant bleeding may occur following trauma or
G. Parizek +3 more
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Jornal Vascular Brasileiro, 2012 A deficiência do fator XI, também conhecida como hemofilia C, é uma doença hematológica hereditária rara, que se manifesta clinicamente com hemorragia persistente após cirurgias, traumas, menorragias e extrações dentárias.
Sergio Quilici Belczak +6 more
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Review Dental Treatment of Patients with Congenital Bleeding Disorders
Česká Stomatologie a Praktické Zubní Lékařství, 2014 Objectives: The commonest congenital bleeding disorders in childhood are hemophilia, von Willebrand disease and deficiency of factor XI. Disease is characterized by a deficient of coagulability. It is a gonosomal recessive condition.
J. Papež, K. Chleborád, T. Dostálová
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Factor XI activity and factor XI antigen in homozygous and heterozygous factor XI deficiency [PDF]
Blood, 1976 A relatively potent antiserum against highly purified, unactivated human factor XI antigen was raised in a rabbit. This antiserum, after concentration, neutralized 50% of the factor XI clotting activity of a standard normal plasma at an antiserum dilution of 1/900.
A, Rimon +3 more
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İstanbul Üniversitesi Veteriner Fakültesi Dergisi, 2016 Factor XI (FXI) is a protein that plays a key role in plasma coagulation. Factor XI Deficiency (FXID) is an autosomal recessive disease caused by an insertion into exon 12 of FXI gene.
Kozet AVANUS, Ahmet ALTINEL
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Acta Médica Portuguesa, 2007 Factor XI deficiency is a rare bleeding disorder in general population, sometimes it can only become clinically evident when patients develop abnormal bleeding after elective surgery. The authors report a clinical case of a 59 year-old woman who after 10
Pedro Conde, Ana Alegria, Andrade Moniz
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Genetics and Molecular Biology, 2007 We investigated the occurrence of Factor XI (FXI) deficiency syndrome in the following Indian dairy animals: Bos taurus Holstein-Friesian and Jersey cattle, Bos indicus Indian cattle breeds, B. taurus x B. indicus crossbreds and the river buffalo Bubalus
Rajesh K. Patel +4 more
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