Brenda Reid
Toronto, ON M5S1A1, Canada
Last Updated: 09/26/2026
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Found 10 publications
A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023.
Journal: Genes
Published: June 07, 2024
Combined immunodeficiency caused by a novel homozygous NFKB1 mutation.
Journal: The Journal of allergy and clinical immunology
Published: May 18, 2020
Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapy.
Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapy.
Journal: Clinical immunology (Orlando, Fla.)
Published: October 02, 2019
Ataxia Telangiectasia Diagnosed on Newborn Screening-Case Cohort of 5 Years' Experience.
Journal: Frontiers in immunology
Published: August 30, 2019
Time-dependent decline of T-cell receptor excision circle levels in ZAP-70 deficiency.
Journal: The journal of allergy and clinical immunology. In practice
Published: May 27, 2019
Long-Term Outcome of Adenosine Deaminase-Deficient Patients-a Single-Center Experience.
Journal: Journal of clinical immunology
Published: April 01, 2017
Hematopoietic stem cell transplantation for RelB deficiency.
Journal: The Journal of allergy and clinical immunology
Published: March 13, 2017
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11).
Journal: The Journal of allergy and clinical immunology
Published: February 20, 2017
Long-term immune reconstitution after matched unrelated hematopoietic stem cell transplantation for immunodeficiency.
Journal: The Journal of allergy and clinical immunology
Published: December 01, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026