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2017, Advances in internal medicine, ISBN 9783319221076, Volume 906., v.
Book
Journal Article
International Journal of Legal Medicine, ISSN 0937-9827, 3/2017, Volume 131, Issue 2, pp. 447 - 458
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 12/2017, Volume 50, Issue 18, pp. 1020 - 1024
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.clinbiochem.2017.07.018 
RISK-FACTORS | PLASMA | VENOUS THROMBOEMBOLISM | THROMBOSIS | GENETICS | INFLAMMATION | THROMBOPHILIA | MEDICAL LABORATORY TECHNOLOGY | EPIDEMIOLOGY | FIBRINOGEN | HIGH-DENSITY-LIPOPROTEIN | Pulmonary embolism | Medical research | Thiols | Blood cholesterol | Analysis | Medicine, Experimental | Family medicine | Thromboembolism | Coronary heart disease
Journal Article
Journal Article
by Yue, YJ and Sun, Q and Xiao, L and Liu, SG and Huang, QJ and Wang, ML and Huo, M and Yang, M and Fu, YY
FRONTIERS IN GENETICS, ISSN 1664-8021, 09/2019, Volume 10
Background and Aims: Genetic variants in the gene SERPINC1 have been shown to be associated with antithrombin deficiency, which subsequently contributes to the... 
pooled systematic analysis | PUBLICATION | VARIANTS | SERPINC1 | THROMBOSIS | antithrombin anticoagulant activity | SUSCEPTIBILITY | REPLICATION | rs2227589 | VENOUS THROMBOEMBOLISM | THROMBOPHILIA | MUTATION | GENETICS & HEREDITY | ANTITHROMBIN | pulmonary embolism | PROTEIN-S | Pulmonary embolism | Genetic aspects | Genes | Genetic polymorphisms
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2017, Volume 173, Issue 9, pp. 2359 - 2365
Patients with overgrowth and complex vascular malformation syndromes, including Proteus syndrome have an increased risk of thromboembolism. Proteus syndrome is... 
thrombosis | pulmonary embolism (PE) | deep vein thrombosis (DVT) | Proteus syndrome | DEEP-VEIN THROMBOSIS | VENOUS MALFORMATIONS | KLIPPEL-TRENAUNAY-SYNDROME | PULMONARY-EMBOLISM | GENETICS & HEREDITY | VASCULAR MALFORMATIONS | THROMBOEMBOLISM | COAGULATION ABNORMALITIES | D-DIMER | ACTIVATING MUTATIONS | CLOVES SYNDROME | Lupus Coagulation Inhibitor - blood | Humans | Middle Aged | Child, Preschool | Male | Antithrombin III Deficiency - genetics | Antithrombin III Deficiency - blood | Proteus Syndrome - blood | Proto-Oncogene Proteins c-akt - genetics | Adult | Female | Thrombosis - blood | Child | Fibrin Fibrinogen Degradation Products - genetics | Protein C Deficiency - blood | Pulmonary Embolism - genetics | Thrombosis - physiopathology | Risk Factors | Pulmonary Embolism - blood | Endothelium, Vascular - metabolism | Proto-Oncogene Proteins c-akt - blood | Adolescent | Endothelium, Vascular - pathology | Proteus Syndrome - physiopathology | Thrombosis - genetics | Aged | Factor V - genetics | Proteus Syndrome - genetics | Protein S Deficiency - blood | Pulmonary Embolism - physiopathology | Thromboembolism | Development and progression | Care and treatment | AKT1 protein | Heterozygotes | Protein C | Thrombosis | Antithrombin | Embolism | Risk factors | Endothelium | Coagulation factors | Factor V | Surgery | Skin | Health risk assessment | Deep vein thrombosis (DVT) | Pulmonary embolism (PE)
Journal Article