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Keywords: Factor X deficiencyClose
Acta Haematol (2021) 144 (2): 176–181.
Published Online: 29 June 2020
... or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Factor X deficiency Genetic analysis Coagulation Compound...
Acta Haematol (2018) 140 (1): 46–50.
Published Online: 16 August 2018
... was diagnosed as suffering from nonsecretory multiple myeloma (MM) complicated by acquired factor X deficiency. A complete response (CR) of the myeloma and recovery of factor X activity (56.6%) were achieved after the administration of treatment, including chemotherapy and bortezomib. We suggest that patients...
Acta Haematol (2013) 129 (1): 40–44.
Published Online: 26 October 2012
...Russell Gollard; Syed Rahman; Ramalingam Ratnasabapathy Factor X inhibitors are rare. The few cases documented in the literature have occurred after viral prodromes, in association with cancer, or after exposure to antibiotics. Acquired factor X deficiencies are also rare and their etiology...
Acta Haematol (1975) 53 (2): 118–127.
Published Online: 04 March 2009
...A. Girolami; P. Coser; A. Brunetti; O. Prinoth A case of classical factor X deficiency is reported. The propositus is a 28-year-old male who presented easy bruising, epistaxis, hematomas, hematuria and occasional hemartrosis since early childhood. The severely prolonged prothrombin time...
Acta Haematol (1976) 56 (5): 307–313.
Published Online: 03 March 2009
...Antonio Girolami; Fabrizio Fabris; Renata Peruffo; Paolo Coser Platelet aggregation to common inductors and to Ristocetin, Thrombo-fax and Ionophore is normal in congenital factor X deficiency and in factor X Friuli coagulation disorder. Washed normal platelets resuspended in the patient’s plasma...
Acta Haematol (1985) 73 (1): 31–36.
Published Online: 25 February 2009
... Key Words. Extrinsic system Factor X abnormality Factor X deficiency Intrinsic system Abstract. A family with a new factor X defect is reported. The proposita is a 56-year-old female. She is asymptomatic and no consanguinity is present between the parents. The main features of the defect...
Acta Haematol (1994) 91 (2): 66–69.
Published Online: 18 February 2009
.... The parents were offspring of two siblings, and their children comprised a nonidentical twin. While the proband demonstrated factor X deficiency, obstructive hypertrophic cardiomyopathy, and primary hypercholesterolemia, her parents and her elder sister were considered heterozygous for factor X. In addition...