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The Journal of Allergy and Clinical Immunology. in Practice|May 25, 2021
A Toolkit and Framework for Optimal Laboratory Evaluation of Individuals with Suspected Primary ImmunodeficiencyVijaya Knight, Jennifer R Heimall, Hey Chong, et al.Blood|February 18, 2017
Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cellsHeinrich Schlums, Moonjung Jung, Hongya Han, et al.Blood|February 17, 2017
Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptomsBianca Tesi, Josef Davidsson, Matthias Voss, et al.Blood|September 21, 2011
Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13DMarie Meeths, Samuel C C Chiang, Stephanie M Wood, et al.Annals of Hematology|November 23, 2024
Clinical spectrum of primary hemophagocytic lymphohistiocytosis: experience of reference centers in Central and Southeast AnatoliaŞefika Akyol, Ebru Yılmaz, Hüseyin Tokgöz, et al.Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.The Journal of Allergy and Clinical Immunology|April 12, 2025
Lipopolysaccharide-responsive and beige-like anchor protein (LRBA) functional deficiency caused by biallelic LRBA missense variants characterized by Evans syndrome or colitisSamuel C C Chiang, Li Yang, Erika Owsley, et al.Blood|July 3, 2024
Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosisSamuel C C Chiang, Laura E Covill, Bianca Tesi, et al.The Journal of Experimental Medicine|May 9, 2024
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defectTamara Kögl, Hsin-Fang Chang, Julian Staniek, et al.Physical Review Letters|October 27, 2011
Search for CP violation in τ±→K(S)0π±ντ decays at BelleM Bischofberger, H Hayashii, K Adamczyk, et al.Pageof 11