UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 35

Sortiert nach

Family Name Adoption in the Dutch Colonies at the Abolition of Slavery in the Context of National Family Name Legislation: A Reflection on Contemporary Name Change

Genealogy (Basel), 2023-12, Vol.7 (4), p.96

Brouwer, Leendert

2023

Link zum Volltext

Verfügbarkeit prüfen

High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin

Thrombosis and haemostasis, 2009-01, Vol.101 (1), p.93

2009

Link zum Volltext

Verfügbarkeit prüfen

High Absolute Risks and Predictors of Venous and Arterial Thromboembolic Events in Patients With Nephrotic Syndrome : Results From a Large Retrospective Cohort Study

Circulation (New York, N.Y.), 2008-01, Vol.117 (2), p.224-230

2008

Link zum Volltext

Verfügbarkeit prüfen

Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives

Blood, 2009-05, Vol.113 (21), p.5314-5322

2009

Link zum Volltext

Verfügbarkeit prüfen

Smart devices to measure and monitor QT intervals

Frontiers in cardiovascular medicine, 2023-11, Vol.10, p.1172666-1172666

2023

Link zum Volltext

Verfügbarkeit prüfen

Hereditary Deficiency of Protein C or Protein S Confers Increased Risk of Arterial Thromboembolic Events at a Young Age : Results From a Large Family Cohort Study

Circulation (New York, N.Y.), 2008-10, Vol.118 (16), p.1659-1667

2008

Link zum Volltext

Verfügbarkeit prüfen

The pathogenesis of venous thromboembolism: evidence for multiple interrelated causes

Annals of internal medicine, 2006-12, Vol.145 (11), p.807

2006

Link zum Volltext

Verfügbarkeit prüfen

Interaction of Hereditary Thrombophilia and Traditional Cardiovascular Risk Factors on the Risk of Arterial Thromboembolism: Pooled Analysis of Four Family Cohort Studies

Circulation. Cardiovascular genetics, 2016-02, Vol.9 (1), p.79

2016

Link zum Volltext

Verfügbarkeit prüfen

The contribution of inherited and acquired thrombophilic defects, alone or combined with antiphospholipid antibodies, to venous and arterial thromboembolism in patients with systemic lupus erythematosus

Blood, 2004-07, Vol.104 (1), p.143-148

2004

Link zum Volltext

Verfügbarkeit prüfen

Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test‐based classification

British journal of haematology, 2005-03, Vol.128 (5), p.703-710

2005

Link zum Volltext

Verfügbarkeit prüfen

Development and validation of a health-related quality-of-life questionnaire in patients with yellow jacket allergy

Journal of allergy and clinical immunology, 2002-01, Vol.109 (1), p.162-170

2002

Link zum Volltext

Verfügbarkeit prüfen

The risk of venous and arterial thrombosis in hyperhomocysteinemic subjects may be a result of elevated factor VIII levels

Haematologica (Roma), 2007-12, Vol.92 (12), p.1703-1706

2007

Link zum Volltext

Verfügbarkeit prüfen

The Clinical Impact of Different Coagulometers on Patient Outcomes

Advances in therapy, 2014-06, Vol.31 (6), p.639-656

2014

Link zum Volltext

Verfügbarkeit prüfen

Contribution of multiple thrombophilic and transient risk factors in the development of cerebral venous thrombosis

Thrombosis research, 2007, Vol.121 (3), p.301-307

2007

Link zum Volltext

Verfügbarkeit prüfen

Reduction of high fetal loss rate by anticoagulant treatment during pregnancy in antithrombin, protein C or protein S deficient women

British journal of haematology, 2007-02, Vol.136 (4), p.656-661

2007

Link zum Volltext

Verfügbarkeit prüfen

Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency

Haematologica (Roma), 2006-08, Vol.91 (8), p.1151

2006

Link zum Volltext

Verfügbarkeit prüfen

High risk of pregnancy‐related venous thromboembolism in women with multiple thrombophilic defects

British journal of haematology, 2007-07, Vol.138 (1), p.110-116

2007

Link zum Volltext

Verfügbarkeit prüfen

The Family Name as Socio-Cultural Feature and Genetic Metaphor: From Concepts to Methods

Human biology, 2012-04, Vol.84 (2), p.169-214

2012

Link zum Volltext

Verfügbarkeit prüfen

Deploying a rapid point-of-care polymerase chain reaction test for SARS-CoV-2 in a clinical research unit to ensure healthy volunteer safety

Bioanalysis, 2021-12, Vol.13 (24), p.1799

2021

Link zum Volltext

Verfügbarkeit prüfen

Bibliography of A. [C.M.] Ton Goeman

Taal en tongval, 2006-01, Vol.19, p.13-23

Brouwer, Leendert

2006

Link zum Volltext

Verfügbarkeit prüfen

Oral contraceptives and the absolute risk of venous thromboembolism in women with single or multiple thrombophilic defects: results from a retrospective family cohort study

Archives of internal medicine (1960), 2007-02, Vol.167 (3), p.282

2007

Link zum Volltext

Verfügbarkeit prüfen

The Family Name as Socio-Cultural Feature and Genetic Metaphor: From Concepts to Methods

Human biology, 2012-04, Vol.84 (2), p.169-214

2012

Link zum Volltext

Verfügbarkeit prüfen

Hereditary Deficiencies of Protein C or Protein S Confer Increased Risk of Arterial Thromboembolic Events at Young Age. Results from a Large Family Cohort Study

Blood, 2008-11, Vol.112 (11), p.422-422

2008

Link zum Volltext

Verfügbarkeit prüfen

Risk of Venous Thromboembolism Is Not Increased by Elevated TAFI Levels

Blood, 2006-11, Vol.108 (11), p.1484-1484

2006

Link zum Volltext

Verfügbarkeit prüfen

Methionine-Loading and Random Homocysteine Tests Have No Added Value in Risk Assessment for Venous and Arterial Thrombosis

Blood, 2006-11, Vol.108 (11), p.1486-1486

2006

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 35

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(33)
Mit Volltextzugriff
(28)

Publikationsform

Artikel
(34)
Berichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(23)
Life Sciences & Biomedicine
(23)
Science & Technology
(23)
Adult
(15)
Female
(15)
Biological And Medical Sciences
(14)
Medical Sciences
(14)
Middle Aged
(14)
Male
(12)
Hematology
(10)
Blood And Lymphatic Vessels
(9)
Cardiology. Vascular System
(9)
Diseases Of The Peripheral Vessels. Diseases Of The Vena Cava. Miscellaneous
(9)
Retrospective Studies
(9)
Risk Factors
(9)
Hematologic And Hematopoietic Diseases
(8)
Incidence
(8)
Aged
(7)
Platelet Diseases And Coagulopathies
(7)
Cohort Studies
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Family Name Adoption in the Dutch Colonies at the Abolition of Slavery in the Context of National Family Name Legislation: A Reflection on Contemporary Name Change

High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin

High Absolute Risks and Predictors of Venous and Arterial Thromboembolic Events in Patients With Nephrotic Syndrome : Results From a Large Retrospective Cohort Study

Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives

Smart devices to measure and monitor QT intervals

Hereditary Deficiency of Protein C or Protein S Confers Increased Risk of Arterial Thromboembolic Events at a Young Age : Results From a Large Family Cohort Study

The pathogenesis of venous thromboembolism: evidence for multiple interrelated causes

Interaction of Hereditary Thrombophilia and Traditional Cardiovascular Risk Factors on the Risk of Arterial Thromboembolism: Pooled Analysis of Four Family Cohort Studies

The contribution of inherited and acquired thrombophilic defects, alone or combined with antiphospholipid antibodies, to venous and arterial thromboembolism in patients with systemic lupus erythematosus

Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test‐based classification

Development and validation of a health-related quality-of-life questionnaire in patients with yellow jacket allergy

The risk of venous and arterial thrombosis in hyperhomocysteinemic subjects may be a result of elevated factor VIII levels

The Clinical Impact of Different Coagulometers on Patient Outcomes

Contribution of multiple thrombophilic and transient risk factors in the development of cerebral venous thrombosis

Reduction of high fetal loss rate by anticoagulant treatment during pregnancy in antithrombin, protein C or protein S deficient women

Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency

High risk of pregnancy‐related venous thromboembolism in women with multiple thrombophilic defects

The Family Name as Socio-Cultural Feature and Genetic Metaphor: From Concepts to Methods

Deploying a rapid point-of-care polymerase chain reaction test for SARS-CoV-2 in a clinical research unit to ensure healthy volunteer safety

Bibliography of A. [C.M.] Ton Goeman

Oral contraceptives and the absolute risk of venous thromboembolism in women with single or multiple thrombophilic defects: results from a retrospective family cohort study

The Family Name as Socio-Cultural Feature and Genetic Metaphor: From Concepts to Methods

Hereditary Deficiencies of Protein C or Protein S Confer Increased Risk of Arterial Thromboembolic Events at Young Age. Results from a Large Family Cohort Study

Risk of Venous Thromboembolism Is Not Increased by Elevated TAFI Levels

Methionine-Loading and Random Homocysteine Tests Have No Added Value in Risk Assessment for Venous and Arterial Thrombosis

Suchergebnisse filtern