Last Updated: 09/26/2026
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Found 11 publications
Correction: A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A.
Journal: Genes and immunity
Published: September 25, 2025
A Scan of Pleiotropic Immune Mediated Disease Genes Identifies Novel Determinants of Baseline FVIII Inhibitor Status in Hemophilia-A.
Journal: Research square
Published: October 27, 2023
A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A.
Journal: Genes and immunity
Published: September 19, 2023
Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function.
Journal: Blood
Published: October 21, 2020
Evaluation of Anticoagulant Monitoring in Pediatric Patients Receiving Enoxaparin for Treatment of Venous Thrombosis.
Journal: The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
Published: July 28, 2020
A Distinctive Approach to Venous Thromboembolism Treatment in a Pediatric, Hemodialysis Patient: A Case Report.
Journal: The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
Published: June 10, 2020
A Cross-Sectional Study of Women and Girls with Congenital Bleeding Disorders: The American Thrombosis and Hemostasis Network Cohort.
Journal: Journal of women's health (2002)
Published: January 07, 2020
Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B.
Journal: Molecular genetics and metabolism
Published: November 06, 2016
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.
Journal: American journal of human genetics
Published: January 14, 2014
Congenital and childhood myeloproliferative disorders with eosinophilia responsive to imatinib.
Journal: Pediatric blood & cancer
Published: December 21, 2011
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Last Updated: 09/26/2026