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PLoS ONE, ISSN 1932-6203, 10/2017, Volume 12, Issue 10, p. e0185785
Background Hereditary thrombophilia (HT) is a genetic predisposition to thrombosis. Asian mutation spectrum of HT is different from Western ones. We... 
POPULATION | FACTOR-V-LEIDEN | RISK-FACTORS | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | PULMONARY-EMBOLISM | MUTATION | DEEP-VEIN THROMBOSIS | ANTITHROMBIN-III | PROTEIN-C | CARRIERS | Protein C Deficiency - complications | Conjunctivitis - genetics | Protein C Deficiency - physiopathology | Humans | Middle Aged | Plasminogen - genetics | Male | Antithrombin III Deficiency - genetics | Antithrombin III - genetics | Skin Diseases, Genetic - genetics | Thrombophilia - etiology | Protein S Deficiency - genetics | Thrombophilia - diagnosis | Antithrombin III Deficiency - physiopathology | Skin Diseases, Genetic - diagnosis | Adult | Female | Retrospective Studies | Antithrombin III Deficiency - complications | Protein S Deficiency - physiopathology | Skin Diseases, Genetic - complications | Antithrombin III Deficiency - diagnosis | Republic of Korea | Venous Thromboembolism - diagnosis | Thrombophilia - genetics | Gene Expression | Protein S Deficiency - complications | Protein S - genetics | Thrombophilia - physiopathology | Sequence Analysis, DNA | Venous Thromboembolism - etiology | Venous Thromboembolism - genetics | Skin Diseases, Genetic - physiopathology | Venous Thromboembolism - physiopathology | Conjunctivitis - physiopathology | Protein C Deficiency - diagnosis | Aged | Protein C Deficiency - genetics | Conjunctivitis - complications | Protein C - genetics | Protein S Deficiency - diagnosis | Conjunctivitis - diagnosis | Plasminogen - deficiency | Type 2 diabetes | Protein C | Genetic aspects | Research | Nucleotide sequencing | Health aspects | DNA sequencing | Hypertension | Anticoagulants | Stroke | Laboratories | Embolisms | Protein deficiency | Antithrombin | Patients | Thrombosis | Gene sequencing | Proteins | Medicine | Thrombophilia | Protein S | Genetics | Diabetes | Mutation | Thromboembolism | Cardiology | Health risk assessment | Deoxyribonucleic acid--DNA | Veins & arteries | Deoxyribonucleic acid | DNA
Journal Article
Kidney International, ISSN 0085-2538, 10/2015, Volume 88, Issue 4, pp. 796 - 803
Journal Article
Pediatric Research, ISSN 0031-3998, 01/2016, Volume 79, Issue 1, pp. 81 - 86
BACKGROUND: The early diagnosis of inherited thrombophilia in children is challenging because of the rarity and hemostatic maturation. METHODS: We explored... 
S DEFICIENCY | PROTEIN-C-DEFICIENCY | VENOUS THROMBOEMBOLISM | LABORATORY CHARACTERISTICS | PLASMA-LEVELS | THROMBOSIS | INHERITED THROMBOPHILIA | PEDIATRICS | COHORT | GENOME-WIDE ASSOCIATION | CHILDREN | Activated Protein C Resistance - epidemiology | Japan - epidemiology | Protein S - analysis | Humans | Child, Preschool | Infant | Male | Antithrombin III Deficiency - genetics | Thromboembolism - epidemiology | Antithrombin III Deficiency - blood | Thrombophilia - epidemiology | Promoter Regions, Genetic - genetics | Antithrombin III - genetics | Protein S Deficiency - genetics | Thrombophilia - diagnosis | Protein C Deficiency - epidemiology | DNA Mutational Analysis | Activated Protein C Resistance - blood | Female | Cerebrovascular Disorders - epidemiology | Activated Protein C Resistance - genetics | Child | Antithrombin III Deficiency - diagnosis | Protein C Deficiency - blood | Thrombophilia - genetics | Protein S - genetics | Antithrombin III Deficiency - epidemiology | Antithrombin III - analysis | Genotype | Protein C - analysis | Thromboembolism - etiology | Cerebrovascular Disorders - etiology | Activated Protein C Resistance - diagnosis | Thrombophilia - blood | Adolescent | Age of Onset | Protein C Deficiency - diagnosis | Protein S Deficiency - epidemiology | Prothrombin - genetics | Factor V - genetics | Protein C Deficiency - genetics | Protein S Deficiency - blood | Protein C - genetics | Protein S Deficiency - diagnosis
Journal Article
Shock (Augusta, Ga.), ISSN 1073-2322, 2009, Volume 31, Issue 3, pp. 280 - 284
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, p. e0152159
Journal Article
Journal Article