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Journal of Thrombosis and Haemostasis : JTH
|
June 22, 2024
Venous thromboembolic disease genetics: from variants to function
Mary Underwood, Christopher Bidlack, Karl C Desch
Thrombosis Research
|
September 26, 2016
Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretion
Mary Underwood, Flora Peyvandi, Isabella Garagiola, et al.
Pediatric Blood & Cancer
|
October 12, 2013
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children
Ayse Metin, Sule Unal, Fatma Gümrük, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
September 6, 2015
ADAMTS13 Secretion and Residual Activity among Patients with Congenital Thrombotic Thrombocytopenic Purpura with and without Renal Impairment
Erica Rurali, Federica Banterla, Roberta Donadelli, et al.
Journal of Thrombosis and Haemostasis : JTH
|
February 19, 2025
Identification of multiple novel procoagulant plasma ligands for stabilin-2
Mary Underwood, Felipe Da Veiga Leprevost, Venkatesha Basrur, et al.
Neurology. Genetics
|
January 15, 2025
Neonatal Encephalopathy: Novel Phenotypes and Genotypes Identified by Genome Sequencing
Anastasia Ambrose, Vanda McNiven, Diane Wilson, et al.
Blood
|
May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
Karl C Desch, Ayse B Ozel, Matt Halvorsen, et al.
Blood
|
May 27, 2014
Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes
Marie Scully, Mari Thomas, Mary Underwood, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Journal of Thrombosis and Haemostasis : JTH
|
June 22, 2024
Venous thromboembolic disease genetics: from variants to function
Mary Underwood, Christopher Bidlack, Karl C Desch
Thrombosis Research
|
September 26, 2016
Degradation of two novel congenital TTP ADAMTS13 mutants by the cell proteasome prevents ADAMTS13 secretion
Mary Underwood, Flora Peyvandi, Isabella Garagiola, et al.
Pediatric Blood & Cancer
|
October 12, 2013
Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children
Ayse Metin, Sule Unal, Fatma Gümrük, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
September 6, 2015
ADAMTS13 Secretion and Residual Activity among Patients with Congenital Thrombotic Thrombocytopenic Purpura with and without Renal Impairment
Erica Rurali, Federica Banterla, Roberta Donadelli, et al.
Journal of Thrombosis and Haemostasis : JTH
|
February 19, 2025
Identification of multiple novel procoagulant plasma ligands for stabilin-2
Mary Underwood, Felipe Da Veiga Leprevost, Venkatesha Basrur, et al.
Neurology. Genetics
|
January 15, 2025
Neonatal Encephalopathy: Novel Phenotypes and Genotypes Identified by Genome Sequencing
Anastasia Ambrose, Vanda McNiven, Diane Wilson, et al.
Blood
|
May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
Karl C Desch, Ayse B Ozel, Matt Halvorsen, et al.
Blood
|
May 27, 2014
Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes
Marie Scully, Mari Thomas, Mary Underwood, et al.
Page
of 1