The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain-Reference-Cited by-同舟云学术

The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain

Published:2009-06 Issue:3 Volume:14 Page:177-181
ISSN:1607-8454
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Girolami Antonio¹,Allemand Emanuele¹,Scandellari Raffaella¹,Lombardi Anna Maria¹,Girolami Bruno¹

Affiliation:

1. University of Padua Medical School Department of Medical and Surgical Sciences, North Eastern Italy Association for the Study of Coagulation Disorders, Padua, Italy

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1179/102453309X426173

Reference27 articles.

1. A ‘New’ Coagulation Defect

2. Stuart Clotting Defect. I. Segregation of an Hereditary Hemorrhagic State from the Heterogeneous Group Heretofore Called “Stable Factor” (SPCA, Proconvertin, Factor VII) Deficiency

3. Über einen neuartigen kongenitalen Gerinnungsdefekt (Mangel an Stuart-Faktor)

4. Heterogeneity of hereditary and acquired factor X deficiencies by combined immunochemical and functional analyses

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1. A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency;Journal of Pediatric Hematology/Oncology;2021-04-26

2. Factor X Deficiency Due to a Compound Heterozygosis Between a New Mutation (Gla72Asp) in Exon 2 and an Already Known one (Gly154Arg) in Exon 5: Factor X Mar Del Plata1);Cardiovascular & Hematological Disorders-Drug Targets;2019-07-05

3. A rare presentation of homozygous factor X deficiency in a pregnant patient: A case report and review of the literature;Haemophilia;2018-12-03

4. Neonatal onset of congenital factor X deficiency;Blood Coagulation & Fibrinolysis;2015-09

5. Complex History of the Discovery and Characterization of Congenital Factor X Deficiency;Seminars in Thrombosis and Hemostasis;2015-04-14