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Blood
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March 22, 2003
Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease
Lee A O'Brien, Paula D James, Maha Othman, et al.
Blood
|
December 28, 2006
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study
Paula D James, Colleen Notley, Carol Hegadorn, et al.
Journal of Developmental Origins of Health and Disease
|
May 20, 2022
Aberrant inflammation in rat pregnancy leads to cardiometabolic alterations in the offspring and intrauterine growth restriction in the F2 generation
Takafumi Ushida, Tiziana Cotechini, Nicole Protopapas, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Karyn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Research and Practice in Thrombosis and Haemostasis
|
March 18, 2021
Harnessing Twitter to empower scientific engagement and communication: The ISTH 2020 virtual congress experience
Maha Othman, Matthew Cormier, Geoffrey D Barnes, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 22, 2024
Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTH
Ross I Baker, Philip Choi, Nicola Curry, et al.
Haematologica
|
September 28, 2019
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study
Francesco Paciullo, Loredana Bury, Patrizia Noris, et al.
Blood
|
April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Ilenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 108) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 108 results.
Blood
|
March 22, 2003
Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease
Lee A O'Brien, Paula D James, Maha Othman, et al.
Blood
|
December 28, 2006
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study
Paula D James, Colleen Notley, Carol Hegadorn, et al.
Journal of Developmental Origins of Health and Disease
|
May 20, 2022
Aberrant inflammation in rat pregnancy leads to cardiometabolic alterations in the offspring and intrauterine growth restriction in the F2 generation
Takafumi Ushida, Tiziana Cotechini, Nicole Protopapas, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Karyn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Research and Practice in Thrombosis and Haemostasis
|
March 18, 2021
Harnessing Twitter to empower scientific engagement and communication: The ISTH 2020 virtual congress experience
Maha Othman, Matthew Cormier, Geoffrey D Barnes, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 22, 2024
Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTH
Ross I Baker, Philip Choi, Nicola Curry, et al.
Haematologica
|
September 28, 2019
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study
Francesco Paciullo, Loredana Bury, Patrizia Noris, et al.
Blood
|
April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Ilenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Page
of 11