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Journal of Clinical Immunology|October 7, 2020
Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates GranulopoiesisEsra Yucel, Ibrahim Serhat Karakus, Ana Krolo, et al.Immunologic Research|April 21, 2024
Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variantsAyca Aykut, Asude Durmaz, Neslihan Karaca, et al.Journal of Clinical Immunology|June 11, 2021
Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and OutcomesOzlem Bayram, Sule Haskologlu, Deniz Bayrakoğlu, et al.Clinical Immunology (Orlando, Fla.)|December 10, 2020
A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitisNurhan Kasap, Velat Celik, Sakine Isik, et al.The Journal of Allergy and Clinical Immunology|June 16, 2018
PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defectsAurélie Berland, Jérémie Rosain, Sophie Kaltenbach, et al.Immunological Reviews|February 24, 2015
Inherited and acquired immunodeficiencies underlying tuberculosis in childhoodStéphanie Boisson-Dupuis, Jacinta Bustamante, Jamila El-Baghdadi, et al.Blood|July 1, 2020
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiencySujal Ghosh, Sevgi Köstel Bal, Emily S J Edwards, et al.Pageof 2