Showing results (181-190 of 243) with videos related to
Sort By:
Pageof 25
Frontiers in Immunology|December 16, 2020
Managing Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders: e-GLILDnet International Clinicians SurveyAnnick A J M van de Ven, Tiago M Alfaro, Alexandra Robinson, et al.The Journal of Allergy and Clinical Immunology|August 12, 2014
Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiencyChristopher C Dvorak, Amel Hassan, Mary A Slatter, et al.Clinical Pharmacology and Therapeutics|November 9, 2019
Proposed Therapeutic Range of Treosulfan in Reduced Toxicity Pediatric Allogeneic Hematopoietic Stem Cell Transplant Conditioning: Results From a Prospective TrialRobert Chiesa, Joseph F Standing, Robert Winter, et al.Journal of Clinical Immunology|October 12, 2022
Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN SurveyMuskan Israni, Bethany Nicholson, Nizar Mahlaoui, et al.Blood Advances|April 6, 2018
Allogeneic hematopoietic stem cell transplantation for severe, refractory juvenile idiopathic arthritisJuliana M F Silva, Fani Ladomenou, Ben Carpenter, et al.Blood Advances|June 4, 2020
New insights into risk factors for transplant-associated thrombotic microangiopathy in pediatric HSCTReem Elfeky, Giovanna Lucchini, Su-Han Lum, et al.The Journal of Clinical Investigation|November 14, 2018
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiencyBertrand Boisson, Yoshitaka Honda, Masahiko Ajiro, et al.Blood|November 1, 2011
IL-21 is the primary common γ chain-binding cytokine required for human B-cell differentiation in vivoMike Recher, Lucinda J Berglund, Danielle T Avery, et al.The Journal of Allergy and Clinical Immunology|April 29, 2014
Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spotsGiancarlo la Marca, Clementina Canessa, Elisa Giocaliere, et al.Journal of Clinical Immunology|August 28, 2024
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.Pageof 25