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The Journal of Allergy and Clinical Immunology|June 6, 2016
Primary Immune Deficiency Treatment Consortium (PIDTC) updateLinda M Griffith, Morton J Cowan, Luigi D Notarangelo, et al.Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Low Exposure Busulfan Conditioning to Achieve Sufficient Multilineage Chimerism in Patients with Severe Combined ImmunodeficiencyChristopher C Dvorak, Janel Long-Boyle, Jasmeen Dara, et al.International Journal of Neonatal Screening|August 18, 2020
Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future SequencingAashish N Adhikari, Robert J Currier, Hao Tang, et al.Journal of Clinical Immunology|January 7, 2021
When Screening for Severe Combined Immunodeficiency (SCID) with T Cell Receptor Excision Circles Is Not SCID: a Case-Based ReviewDavid Buchbinder, Jolan E Walter, Manish J Butte, et al.American Journal of Hematology|August 4, 2007
Pyrimethamine treatment does not ameliorate lymphoproliferation or autoimmune disease in MRL/lpr-/- mice or in patients with autoimmune lymphoproliferative syndromeV Koneti Rao, Kennichi C Dowdell, Janet K Dale, et al.The Journal of Allergy and Clinical Immunology|October 24, 2007
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification CommitteeRaif S Geha, Luigi D Notarangelo, Jean-Laurent Casanova, et al.Journal of Clinical Immunology|January 29, 2015
Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantationDivya Punwani, Haopeng Wang, Alice Y Chan, et al.BMC Medical Genetics|July 4, 2007
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type IbLilia L Bi, George Pan, T Prescott Atkinson, et al.Blood|April 3, 2010
Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndromeKennichi C Dowdell, Julie E Niemela, Susan Price, et al.The Journal of Experimental Medicine|January 20, 2016
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Alice Y Chan, Divya Punwani, Theresa A Kadlecek, et al.Pageof 16