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Blood
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November 24, 2025
Multisite Validation of a Venous Thrombosis Risk Model in Critically Ill Children Through the CHAT Consortium
Julie Jaffray, Brian R Branchford, Maua Mosha Alleyne, et al.
Seminars in Thrombosis and Hemostasis
|
September 19, 2024
Secondary Anticoagulation Use in Patients < 21 Years Old following Primary Anticoagulant Treatment for Provoked Venous Thromboembolism: Findings from the Kids-DOTT Trial
Hope P Wilson, Maua Mosha, Alexandra Miller, et al.
Blood Advances
|
September 25, 2024
Outcomes in children with provoked venous thrombosis and antiphospholipid antibodies: findings from the Kids-DOTT trial
Marisol Betensky, Maua Mosha, Cristina Tarango, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 16, 2025
Risks of incident venous thromboembolism, recurrent thromboembolism, and use of antithrombotic therapies among children with congenital heart disease undergoing cardiac surgery: a global multicenter analysis of real-world data
Amy L Kiskaddon, Nhue L Do, Ernest K Amankwah, et al.
Thrombosis and Haemostasis
|
June 28, 2016
Bivariate evaluation of thromboembolism and bleeding in clinical trials of anticoagulants in patients with atrial fibrillation
John M Kittelson, Philippe Gabriel Steg, Jonathan L Halperin, et al.
Circulation
|
September 24, 2014
The postthrombotic syndrome: evidence-based prevention, diagnosis, and treatment strategies: a scientific statement from the American Heart Association
Susan R Kahn, Anthony J Comerota, Mary Cushman, et al.
JAMIA Open
|
September 3, 2024
Leveraging a global, federated, real-world data network to optimize investigator-initiated pediatric clinical trials: the TriNetX Pediatric Collaboratory Network
Jurran L Wilson, Marisol Betensky, Sharda Udassi, et al.
Thrombosis Research
|
February 28, 2024
Considerations for instituting pediatric pulmonary embolism response teams: A tool kit
Madhvi Rajpurkar, Rachel P Rosovsky, Suzan Williams, et al.
Journal of Medical Genetics
|
March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol, S Lebon, P Bénit, et al.
Journal of Thrombosis and Haemostasis : JTH
|
April 26, 2023
Evaluation of venous thromboembolism risk factors reveals subtype heterogenicity in children with central venous catheters: a multicenter study from the Children's Hospital Acquired Thrombosis consortium
Julie Jaffray, Maua Mosha, Brian Branchford, et al.
Page
of 38
Search research articles
Search
Showing results (311-320 of 380) with videos related to
Sort By:
Page
of 38
Blood
|
November 24, 2025
Multisite Validation of a Venous Thrombosis Risk Model in Critically Ill Children Through the CHAT Consortium
Julie Jaffray, Brian R Branchford, Maua Mosha Alleyne, et al.
Seminars in Thrombosis and Hemostasis
|
September 19, 2024
Secondary Anticoagulation Use in Patients < 21 Years Old following Primary Anticoagulant Treatment for Provoked Venous Thromboembolism: Findings from the Kids-DOTT Trial
Hope P Wilson, Maua Mosha, Alexandra Miller, et al.
Blood Advances
|
September 25, 2024
Outcomes in children with provoked venous thrombosis and antiphospholipid antibodies: findings from the Kids-DOTT trial
Marisol Betensky, Maua Mosha, Cristina Tarango, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 16, 2025
Risks of incident venous thromboembolism, recurrent thromboembolism, and use of antithrombotic therapies among children with congenital heart disease undergoing cardiac surgery: a global multicenter analysis of real-world data
Amy L Kiskaddon, Nhue L Do, Ernest K Amankwah, et al.
Thrombosis and Haemostasis
|
June 28, 2016
Bivariate evaluation of thromboembolism and bleeding in clinical trials of anticoagulants in patients with atrial fibrillation
John M Kittelson, Philippe Gabriel Steg, Jonathan L Halperin, et al.
Circulation
|
September 24, 2014
The postthrombotic syndrome: evidence-based prevention, diagnosis, and treatment strategies: a scientific statement from the American Heart Association
Susan R Kahn, Anthony J Comerota, Mary Cushman, et al.
JAMIA Open
|
September 3, 2024
Leveraging a global, federated, real-world data network to optimize investigator-initiated pediatric clinical trials: the TriNetX Pediatric Collaboratory Network
Jurran L Wilson, Marisol Betensky, Sharda Udassi, et al.
Thrombosis Research
|
February 28, 2024
Considerations for instituting pediatric pulmonary embolism response teams: A tool kit
Madhvi Rajpurkar, Rachel P Rosovsky, Suzan Williams, et al.
Journal of Medical Genetics
|
March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency
M Chol, S Lebon, P Bénit, et al.
Journal of Thrombosis and Haemostasis : JTH
|
April 26, 2023
Evaluation of venous thromboembolism risk factors reveals subtype heterogenicity in children with central venous catheters: a multicenter study from the Children's Hospital Acquired Thrombosis consortium
Julie Jaffray, Maua Mosha, Brian Branchford, et al.
Page
of 38