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The Journal of Allergy and Clinical Immunology|July 12, 2015
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficienciesCindy S Ma, Natalie Wong, Geetha Rao, et al.
The Journal of Allergy and Clinical Immunology|December 31, 2019
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) scoreVictoria Katharina Tesch, Hassan Abolhassani, Bella Shadur, et al.
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.
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.
The Journal of Experimental Medicine|August 26, 2015
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndromeAlexandra Y Kreins, Michael J Ciancanelli, Satoshi Okada, 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.
Human Mutation|November 8, 2006
Schimke immunoosseous dysplasia: suggestions of genetic diversityJ Marietta Clewing, Helen Fryssira, David Goodman, et al.
The Journal of Experimental Medicine|July 6, 2011
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasisLuyan Liu, Satoshi Okada, Xiao-Fei Kong, 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.
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