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SERPINC1 gene mutations in antithrombin deficiency

British journal of haematology, 2017-07, Vol.178 (2), p.279-285

2017

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Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin ( F2 ) gene mutation in a Dutch Caucasian family with unexplained thrombosis

Haematologica (Roma), 2020-07, Vol.105 (7), p.e370-e372

2020

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Monitoring of heparins in antithrombin-deficient patients

Thrombosis research, 2019-03, Vol.175, p.8-12

2019

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Direct Oral Anticoagulants in Antithrombin Deficiency: Initial Experience in a Single Center

Thrombosis and haemostasis, 2021-02, Vol.121 (2), p.242-245

2021

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Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples

International journal of laboratory hematology, 2021-06, Vol.43 (3), p.e101-e103

2021

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β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study

Thrombosis research, 2018-08, Vol.168, p.47-52

2018

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Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis

Blood advances, 2020-12, Vol.4 (24), p.6353-6363

2020

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Factor 11 single-nucleotide variants in women with heavy menstrual bleeding

Journal of obstetrics and gynaecology, 2017-10, Vol.37 (7), p.912-918

2017

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Familial macrothrombocytopenia due to a double mutation in cis in the alpha‐actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura

Pediatric blood & cancer, 2018-12, Vol.65 (12), p.e27418-n/a

2018

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Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study

Blood advances, 2023-04, Vol.7 (7), p.1269-1278

2023

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Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency

Thrombosis and haemostasis, 2013-06, Vol.109 (6), p.1183-1185

2013

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Understanding the functional difference between growth arrest-specific protein 6 and protein S: an evolutionary approach

Open biology, 2014-10, Vol.4 (10), p.140121

2014

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Low cut-off values increase diagnostic performance of protein S assays

Thrombosis and haemostasis, 2010-09, Vol.104 (3), p.618-625

2010

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Competitiveness of Chinese Industries - A Comparison with the EU

Review of European studies, 2012-02, Vol.4 (1)

2012

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PROS1 Heerlen polymorphism is associated with increased free plasma tissue factor pathway inhibitor levels

Thrombosis and haemostasis, 2012-03, Vol.107 (3), p.594-596

2012

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High protein S activity due to C4b‐binding protein deficiency in a 34‐year‐old Surinamese female with ischemic retinopathy

Clinical case reports, 2018-05, Vol.6 (5), p.935-938

2018

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Decreased free protein S levels and venous thrombosis in the acute setting, a case-control study

Thrombosis research, 2011-11, Vol.128 (5), p.501-502

2011

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Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: Results from a retrospective family cohort study

Thrombosis research, 2010-10, Vol.126 (4), p.e249-e254

2010

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TEMPORARY REMOVAL: Direct oral anticoagulants in antithrombin deficiency: initial experience in a single center

Thrombosis and haemostasis

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Clinical relevance of decreased free protein S levels: results from a retrospective family cohort study involving 1143 relatives

Blood, 2009-02, Vol.113 (6), p.1225-1230

2009

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Free Protein S Levels on the Risk of First Venous Thrombosis and Recurrence. Results from a Retrospective Family Cohort Study in 1143 Relatives

Blood, 2008-11, Vol.112 (11), p.1808-1808

2008

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Associations Between Free Protein S and Factor VIII Levels with Traditional Arterial Thrombotic Risk Factors and Their Risk On Arterial Thrombosis. Results From a Retrospective Family Cohort Study

Blood, 2009-11, Vol.114 (22), p.25-25

2009

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SERPINC 1 gene mutations in antithrombin deficiency

British journal of haematology, 2017-07, Vol.178 (2), p.279-285

2017

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UNERGATIVES AS COPULAR VERBS; LOCATIONAL AND EXISTENTIAL PREDICATION

Linguistic review, 1990, Vol.7 (1), p.1-80

1990

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Single-Nucleotide Variation Spectrum of the Factor XI Gene in Women with Heavy Menstrual Bleeding

Blood, 2014-12, Vol.124 (21), p.4213-4213

2014

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SERPINC1 gene mutations in antithrombin deficiency

Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin ( F2 ) gene mutation in a Dutch Caucasian family with unexplained thrombosis

Monitoring of heparins in antithrombin-deficient patients

Direct Oral Anticoagulants in Antithrombin Deficiency: Initial Experience in a Single Center

Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples

β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study

Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis

Factor 11 single-nucleotide variants in women with heavy menstrual bleeding

Familial macrothrombocytopenia due to a double mutation in cis in the alpha‐actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura

Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study

Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency

Understanding the functional difference between growth arrest-specific protein 6 and protein S: an evolutionary approach

Low cut-off values increase diagnostic performance of protein S assays

Competitiveness of Chinese Industries - A Comparison with the EU

PROS1 Heerlen polymorphism is associated with increased free plasma tissue factor pathway inhibitor levels

High protein S activity due to C4b‐binding protein deficiency in a 34‐year‐old Surinamese female with ischemic retinopathy

Decreased free protein S levels and venous thrombosis in the acute setting, a case-control study

Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: Results from a retrospective family cohort study

TEMPORARY REMOVAL: Direct oral anticoagulants in antithrombin deficiency: initial experience in a single center

Clinical relevance of decreased free protein S levels: results from a retrospective family cohort study involving 1143 relatives

Free Protein S Levels on the Risk of First Venous Thrombosis and Recurrence. Results from a Retrospective Family Cohort Study in 1143 Relatives

Associations Between Free Protein S and Factor VIII Levels with Traditional Arterial Thrombotic Risk Factors and Their Risk On Arterial Thrombosis. Results From a Retrospective Family Cohort Study

SERPINC 1 gene mutations in antithrombin deficiency

UNERGATIVES AS COPULAR VERBS; LOCATIONAL AND EXISTENTIAL PREDICATION

Single-Nucleotide Variation Spectrum of the Factor XI Gene in Women with Heavy Menstrual Bleeding

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