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Periprocedural management of type 2N von Willebrand disease with efanesoctocog alfa

Journal of thrombosis and haemostasis, 2023-12, Vol.21 (12), p.3508-3510

2023

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Readability of Spine-Related Patient Education Materials From Leading Orthopedic Academic Centers

Spine (Philadelphia, Pa. 1976), 2016-05, Vol.41 (9), p.E561-E565

2016

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PTPMT1 Inhibition Lowers Glucose through Succinate Dehydrogenase Phosphorylation

Cell reports (Cambridge), 2015-02, Vol.10 (5), p.694-701

2015

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Natural Language Processing of Serum Protein Electrophoresis Reports in the Veterans Affairs Health Care System

JCO clinical cancer informatics, 2020-08 (4), p.749-756

2020

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Chemical and metabolomic screens identify novel biomarkers and antidotes for cyanide exposure

The FASEB journal, 2013-05, Vol.27 (5), p.1928-1938

2013

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Induced and Sustained Hypernatremia for the Prevention and Treatment of Cerebral Edema Following Brain Injury

Neurocritical care, 2013-10, Vol.19 (2), p.222-231

2013

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Predictors of relapse and efficacy of rituximab in immune thrombotic thrombocytopenic purpura

Blood advances, 2019-05, Vol.3 (9), p.1512-1518

2019

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Overall Survival of Warfarin Compared to LMWH/Doacs in Cancer-Associated Venous Thromboembolism: VA Cohort Study

Blood, 2023-11, Vol.142 (Supplement 1), p.138-138

2023

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Clinical Consequences of Rare Germline Variation in Genes Associated with Coagulation across 451,958 Individuals

Blood, 2023-11, Vol.142 (Supplement 1), p.3972-3972

2023

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Coagulation Factor XII ( F12 ) Haploinsufficiency Is Protective Against Venous Thromboembolism in 415,921 Individuals

Blood, 2023-11, Vol.142 (Supplement 1), p.805-805

2023

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Rare Germline Loss-of-Function Variants in HSP47 ( SERPINH1 ) Are Associated with an Intermediate Osteogenesis Imperfecta Phenotype Characterized By Atopic Inflammation and Increased Risk of Thrombosis

Blood, 2023-11, Vol.142 (Supplement 1), p.3934-3934

2023

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Meta-Analysis of National-Level Genotyping Datasets to Determine the Risk of Thrombosis in Double Heterozygous Carriers of Factor V Leiden and the Prothrombin G20210A Mutation across 876,417 Individuals

Blood, 2023-11, Vol.142 (Supplement 1), p.806-806

2023

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Protein Z ( PROZ ) Loss of Function Is Associated with Increased Risk of Ischemic Stroke in 416,767 UK Biobank Participants

Blood, 2023-11, Vol.142 (Supplement 1), p.2611-2611

2023

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Circulating tumor DNA predicts venous thromboembolism in patients with cancers

Journal of thrombosis and haemostasis, 2024-09

2024

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Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank

Blood, 2024-03

2024

Volltextzugriff (PDF)

Predictors of Relapse and Efficacy of Rituximab in Autoimmune Thrombotic Thrombocytopenic Purpura (TTP): A Multi-Institutional Registry-Based Analysis

Blood, 2018-11, Vol.132 (Supplement 1), p.375-375

2018

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Cationic zinc is required for factor XII recruitment and activation by stimulated platelets and for thrombus formation in vivo

Journal of thrombosis and haemostasis, 2020-09, Vol.18 (9), p.2318-2328

2020

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Deaths and complications associated with the management of acute immune thrombotic thrombocytopenic purpura

Transfusion (Philadelphia, Pa.), 2020-04, Vol.60 (4), p.841-846

2020

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Rare Inherited Defects of the Complement System in Purpura Fulminans

Blood, 2020-11, Vol.136 (Supplement 1), p.35-36

2020

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Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program

Journal of human genetics, 2023-08, Vol.68 (8), p.565-570

2023

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PTPMT1 Inhibition Lowers Glucose Through Phosphorylation of SDH

Cell reports (Cambridge), 2015-02, Vol.10 (5), p.694-701

2015

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Periprocedural management of type 2N von Willebrand disease with efanesoctocog alfa

Journal of thrombosis and haemostasis : JTH, 2023, Vol.21 (12), p.3508-3510

2023

Volltextzugriff (PDF)

ECOSTRESS: NASA's Next Generation Mission to Measure Evapotranspiration From the International Space Station

Water resources research, 2020-04, Vol.56 (4), p.n/a

2020

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Periprocedural management of type 2N von Willebrand disease with efanesoctocog alfa

Readability of Spine-Related Patient Education Materials From Leading Orthopedic Academic Centers

PTPMT1 Inhibition Lowers Glucose through Succinate Dehydrogenase Phosphorylation

Natural Language Processing of Serum Protein Electrophoresis Reports in the Veterans Affairs Health Care System

Chemical and metabolomic screens identify novel biomarkers and antidotes for cyanide exposure

Induced and Sustained Hypernatremia for the Prevention and Treatment of Cerebral Edema Following Brain Injury

Predictors of relapse and efficacy of rituximab in immune thrombotic thrombocytopenic purpura

Overall Survival of Warfarin Compared to LMWH/Doacs in Cancer-Associated Venous Thromboembolism: VA Cohort Study

Clinical Consequences of Rare Germline Variation in Genes Associated with Coagulation across 451,958 Individuals

Coagulation Factor XII ( F12 ) Haploinsufficiency Is Protective Against Venous Thromboembolism in 415,921 Individuals

Rare Germline Loss-of-Function Variants in HSP47 ( SERPINH1 ) Are Associated with an Intermediate Osteogenesis Imperfecta Phenotype Characterized By Atopic Inflammation and Increased Risk of Thrombosis

Meta-Analysis of National-Level Genotyping Datasets to Determine the Risk of Thrombosis in Double Heterozygous Carriers of Factor V Leiden and the Prothrombin G20210A Mutation across 876,417 Individuals

Protein Z ( PROZ ) Loss of Function Is Associated with Increased Risk of Ischemic Stroke in 416,767 UK Biobank Participants

Circulating tumor DNA predicts venous thromboembolism in patients with cancers

Thrombosis Risk in Double Heterozygous Carriers of Factor V Leiden and Prothrombin G20210A in FinnGen and the UK Biobank

Predictors of Relapse and Efficacy of Rituximab in Autoimmune Thrombotic Thrombocytopenic Purpura (TTP): A Multi-Institutional Registry-Based Analysis

Cationic zinc is required for factor XII recruitment and activation by stimulated platelets and for thrombus formation in vivo

Low-frequency inherited complement receptor variants are associated with purpura fulminans

Deaths and complications associated with the management of acute immune thrombotic thrombocytopenic purpura

Rare Inherited Defects of the Complement System in Purpura Fulminans

Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program

PTPMT1 Inhibition Lowers Glucose Through Phosphorylation of SDH

Periprocedural management of type 2N von Willebrand disease with efanesoctocog alfa

ECOSTRESS: NASA's Next Generation Mission to Measure Evapotranspiration From the International Space Station

Finding individualised treatment in obese needing enoxaparin (FIT ONE): a multicentre study of therapeutic enoxaparin and the role of anti-factor Xa monitoring

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