Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Steven A. Austin"'
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 5, Pp n/a-n/a (2021)
Abstract Background Coagadex is a high‐purity plasma‐derived factor X concentrate (pdFX) developed to treat hereditary factor X deficiency (FXD). Objective Evaluate the efficacy and safety of pdFX administered to patients with hereditary FXD. Met
Externí odkaz:
https://doaj.org/article/4e9290cfd4a24635a61529d807f095f6
Autor:
Steven K. Austin
Publikováno v:
Medicine. 49:199-204
Autor:
Miranda Norton, Kaan Kavakli, Michael Gattens, Jeanette Payne, Steven K. Austin, Michael J. Mitchell, Ri Liesner
Publikováno v:
Blood Coagulation & Fibrinolysis. 30:34-41
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The objective was to examine the genotypic and phenotypic characteristics of individuals with hereditary factor X deficiency (FXD), a rare autosomal recessive bleeding disorder caused by mutations in the F10 gene located on chromosome 1
The objective was to examine the genotypic and phenotypic characteristics of individuals with hereditary factor X deficiency (FXD), a rare autosomal recessive bleeding disorder caused by mutations in the F10 gene located on chromosome 1
Autor:
Steven Arthur Austin, Roger W. Sanders
Publikováno v:
The Proceedings of the International Conference on Creationism. 8:525-552
Autor:
Steven Arthur Austin, Roger W. Sanders
Publikováno v:
The Proceedings of the International Conference on Creationism. 8:277-286
Autor:
Ri Liesner, Kaan Kavakli, Guenter Auerswald, Steven K. Austin, Flora Peyvandi, Carolyn M. Millar, María Teresa Álvarez Román
Publikováno v:
Blood Reviews. 50:100833
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology and severity of the associated bleeding symptoms are highly heterogeneous, adding to the difficulties of diagnosis and management. Evidence-based guid
Autor:
Steven K. Austin
Publikováno v:
Medicine. 45:204-208
Autor:
Steven K. Austin, Vickie McDonald
Publikováno v:
Medicine. 45:229-232
The most common inherited disorders of coagulation are von Willebrand disease (VWD), haemophilia A and haemophilia B. Haemophilia A and B are sex-linked disorders, whereas VWD is inherited in an autosomal fashion. Definitive diagnosis is made using c
Publikováno v:
Medical Care. 53:e65-e72
Background Comorbidity adjustment is an important component of health services research and clinical prognosis. When adjusting for comorbidities in statistical models, researchers can include comorbidities individually or through the use of summary m
Autor:
Steven K. Austin
Publikováno v:
Medicine. 41:208-211