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The Journal of Allergy and Clinical Immunology|March 1, 2015
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiencyKarin R Engelhardt, Michael E Gertz, Sevgi Keles, et al.Frontiers in Immunology|October 19, 2017
Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.The Journal of Allergy and Clinical Immunology. in Practice|October 20, 2022
The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of ImmunitySafa Baris, Hassan Abolhassani, Michel J Massaad, et al.Frontiers in Immunology|August 4, 2017
Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56<sup>bright</sup> NKG2A<sup>+++</sup> Cells, and Yet Display Increased Degranulation and Higher Perforin ContentKerry Dobbs, Giovanna Tabellini, Enrica Calzoni, et al.The Journal of Allergy and Clinical Immunology|August 18, 2023
Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiencyNigar Taghizade, Royala Babayeva, Altan Kara, et al.The Journal of Allergy and Clinical Immunology|September 17, 2017
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiencyHassan Abolhassani, Janet Chou, Wayne Bainter, et al.Science Immunology|June 17, 2018
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activityVivien Béziat, Juan Li, Jian-Xin Lin, et al.Journal of Clinical Immunology|January 29, 2015
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patientsSusanne E Aydin, Sara Sebnem Kilic, Caner Aytekin, et al.Frontiers in Genetics|August 27, 2025
Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registryZahra Chavoshzadeh, Shahrzad Fallah, Vahide Zeinali, et al.The Journal of Experimental Medicine|March 25, 2020
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeVivien Béziat, Simon J Tavernier, Yin-Huai Chen, et al.Pageof 10