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The Journal of Clinical Investigation|September 20, 2016
FOXP3+ Tregs require WASP to restrain Th2-mediated food allergyWillem S Lexmond, Jeremy A Goettel, Jonathan J Lyons, et al.
Blood|July 19, 2017
Gene therapy for Wiskott-Aldrich syndrome in a severely affected adultEmma C Morris, Thomas Fox, Ronjon Chakraverty, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2010
Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitisLena F Schimke, Julie Sawalle-Belohradsky, Joachim Roesler, et al.
Journal of Clinical Immunology|January 5, 2019
Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair DisordersDavid Buchbinder, Fabian Hauck, Michael H Albert, et al.
Journal of Clinical Immunology|May 10, 2013
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedsideAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.
Journal of Clinical Immunology|December 12, 2017
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of ImmunityCapucine Picard, H Bobby Gaspar, Waleed Al-Herz, et al.
Journal of Clinical Immunology|October 9, 2015
The 2015 IUIS Phenotypic Classification for Primary ImmunodeficienciesAziz Bousfiha, Leïla Jeddane, Waleed Al-Herz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 5, 2012
Valproic acid confers functional pluripotency to human amniotic fluid stem cells in a transgene-free approachDafni Moschidou, Sayandip Mukherjee, Michael P Blundell, et al.
Blood|February 11, 2020
Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programsEmmanuelle Six, Agathe Guilloux, Adeline Denis, et al.
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