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The New England Journal of Medicine|December 8, 2025
Prime Editing for p47phox-Deficient Chronic Granulomatous DiseaseJennifer L Gori, Elie Haddad, Haydar Frangoul, et al.
Annals of the Rheumatic Diseases|May 21, 2014
The outcomes of juvenile idiopathic arthritis in children managed with contemporary treatments: results from the ReACCh-Out cohortJaime Guzman, Kiem Oen, Lori B Tucker, et al.
Arthritis Care & Research|April 15, 2010
Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohortKiem Oen, Ciarán M Duffy, Shirley M L Tse, et al.
Gastroenterology|February 3, 2016
Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel DiseaseQi Li, Cheng Hiang Lee, Lauren A Peters, et al.
Journal of Clinical Immunology|July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic LymphohistiocytosisAnnaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
The New England Journal of Medicine|July 31, 2014
Transplantation outcomes for severe combined immunodeficiency, 2000-2009Sung-Yun Pai, Brent R Logan, Linda M Griffith, et al.
Transplantation and Cellular Therapy|October 4, 2025
Umbilical Cord Blood Transplantation Provides an Alternative for Patients With Chronic Granulomatous Disease Lacking HLA-Matched Donors: A PIDTC ReportDanielle E Arnold, Jennifer W Leiding, Brent Logan, et al.
The Journal of Allergy and Clinical Immunology|January 30, 2024
Allogeneic hematopoietic cell transplantation is effective for p47phox chronic granulomatous disease: A Primary Immune Deficiency Treatment Consortium studyEyal Grunebaum, Danielle E Arnold, Brent Logan, et al.
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