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Journal Article
1991, 1991 ed. --, ISBN 0849342317, 1 v. (various pagings)
Book
Chinese Journal of Medical Genetics, ISSN 1003-9406, 04/2016, Volume 33, Issue 2, pp. 160 - 163
Journal Article
Annales de Biologie Clinique, ISSN 0003-3898, 07/2016, Volume 74, Issue 4, pp. 405 - 412
Journal Article
1994, 1994 ed., ISBN 9780849389986, 423
Book
Journal of Atherosclerosis and Thrombosis, ISSN 1340-3478, 2015
Aim: We report the study of a familial rare disease with recurrent venous thromboembolic events that remained undiagnosed for many years using standard... 
Coagulation | Fibrinogen | Genetics | Thrombosis | Dysfibrinogenemia
Journal Article
by Luo, ML and Wei, AQ and Xiang, LQ and Yan, J and Liao, L and Deng, XL and Deng, DH and Cheng, P and Lin, FQ
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, ISSN 0929-5305, 10/2018, Volume 46, Issue 3, pp. 409 - 419
We found a heterozygous dysfibrinogenemia caused by a substitution of A alpha Arg16Cys. The proband suffered multiple cerebral infarctions. Routine coagulation... 
MANAGEMENT | POLYMERIZATION | CLINICAL-FEATURES | Thrombosis | FIBRINOPEPTIDE | Dysfibrinogenemia | FIBRINOLYSIS | CONGENITAL DYSFIBRINOGENEMIA | Fibrinogen | THROMBOPHILIA | THROMBOTIC DISEASE | PERIPHERAL VASCULAR DISEASE | MUTATIONS | HEMATOLOGY | MOLECULAR-MECHANISMS
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 12/2018, Volume 35, Issue 6, pp. 812 - 814
To study the clinical phenotype and gene mutation analysis of a hereditary abnormal fibrinogenemia family and explore its molecular pathogenesis. The STA-R... 
Polymerase chain reaction | Mutation | Fug gene | Hereditary dysfibrinogenemia
Journal Article
European Journal of Haematology, ISSN 0902-4441, 10/2019, Volume 103, Issue 4, pp. 379 - 384
Objectives Inherited dysfibrinogenemia is a rare disorder, for which clinical studies related to the risk of bleeding or thrombosis and the type of causative... 
thrombophilia | dysfibrinogenemia | inherited bleeding disorders | fibrinogen | gene mutation | Pregnancy | Ischemia | Fibrinogen | Mutation | Thromboembolism | Health risk assessment | Thrombosis | Bleeding
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 04/2014, Volume 31, Issue 2, pp. 134 - 139
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 11/2018, Volume 118, Issue 11, pp. 1867 - 1874
Abstract Background  Numerous mutations in FGA , FGB or FGG lead to congenital fibrinogen disorders (CFDs), but their epidemiology is not well characterized.... 
Coagulation and Fibrinolysis | afibrinogenemia | hypofibrinogenemia | mutation | dysfibrinogenemia | congenital | hypodysfibrinogenaemia | BLEEDING DISORDERS | STORAGE | DIAGNOSIS | MANAGEMENT | DEFICIENCIES | THROMBOPHILIA | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | hypodysfibrino-genaemia
Journal Article
Journal of Clinical Pathology, ISSN 0021-9746, 02/2019, Volume 72, Issue 2, pp. 177 - 180
Most fibrinogen replacement strategies focus on quantitative deficiencies. A thrombin time (TT) mixing study helped to assess qualitative defects caused by... 
dysfibrinogenemia | fibrinogen | thrombin time | cryoprecipitate | PATHOLOGY | Studies | Antigens | Carbohydrates | Liver diseases | Laboratories | Patients | Thrombosis | Binding sites
Journal Article
Acta Bioquimica Clinica Latinoamericana, ISSN 0325-2957, 06/2016, Volume 50, Issue 2, pp. 215 - 221
Journal Article
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