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Journal of Clinical Immunology|June 21, 2022
A Novel CEBPE Variant Causes Severe Infections and Profound NeutropeniaAaqib Zaffar Banday, Anit Kaur, Tadayuki Akagi, et al.Journal of Clinical Immunology|June 21, 2022
Severe Combined Immunodeficiency (SCID) Screening in Arizona: Lessons Learned from the First 2 YearsNatalie A Booth, Catherine M Freeman, Benjamin L Wright, et al.Journal of Clinical Immunology|June 3, 2021
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 DeficiencyJohannes Raedler, Thomas Magg, Meino Rohlfs, et al.Journal of Clinical Immunology|January 4, 2021
IKAROS-Associated Diseases in 2020: Genotypes, Phenotypes, and Outcomes in Primary Immune Deficiency/Inborn Errors of ImmunityHye Sun Kuehn, Cristiane J Nunes-Santos, Sergio D RosenzweigJournal of Clinical Immunology|September 1, 1987
Increased presence of common systemic lupus erythematosus (SLE) anti-DNA idiotypes (16/6 Id, 32/15 Id) is induced by procainamideY Shoenfeld, Y Vilner, T Reshef, et al.Journal of Clinical Immunology|June 8, 2017
The Use of Salmonella Typhim Vaccine to Diagnose Antibody DeficiencyMary T Bausch-Jurken, James W Verbsky, Katherine A Gonzaga, et al.Journal of Clinical Immunology|October 19, 2021
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG PatientsCristina Cifaldi, Beatrice Rivalta, Donato Amodio, et al.Journal of Clinical Immunology|March 1, 1986
Clinical and laboratory features of patients with an inherited deficiency of neutrophil membrane complement receptor type 3 (CR3) and the related membrane antigens LFA-1 and p150,95G D RossJournal of Clinical Immunology|October 7, 2021
Long-Term Experience of Subcutaneous Immunoglobulin Therapy in Pediatric Primary Immunodeficient Patients with Low and Normal Body WeightYahya Gul, Hasan Kapakli, Sukru Nail Guner, et al.Journal of Clinical Immunology|October 17, 2021
Hyper-IgE Syndrome due to an Elusive Novel Intronic Homozygous Variant in DOCK8Stuart G Tangye, Paul E Gray, Bethany A Pillay, et al.Pageof 349