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Clinical Immunology (Orlando, Fla.)|January 7, 2021
SARS-CoV-2 infection associated with hepatitis in an infant with X-linked severe combined immunodeficiencyNicolai S C van Oers, Natasha W Hanners, Paul K Sue, et al.
Clinical Case Reports|September 13, 2021
Lymphomatoid granulomatosis of the central nervous system (CNS-LYG) posing a management challengeMohsin Soleja, Jesse Manuel Jaso, Weina Chen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 9, 2004
Differential roles for CCR5 expression on donor T cells during graft-versus-host disease based on pretransplant conditioningChristian A Wysocki, Susan B Burkett, Angela Panoskaltsis-Mortari, et al.
The Journal of Allergy and Clinical Immunology|July 7, 2023
Comprehensive phenotypic analysis of diverse FOXN1 variantsAngela Moses, Pratibha Bhalla, Austin Thompson, et al.
The Journal of Clinical Investigation|January 18, 2022
Cytoplasmic RNA quality control failure engages mTORC1-mediated autoinflammatory diseaseKun Yang, Jie Han, Mayumi Asada, et al.
The Journal of Clinical Investigation|September 22, 2022
Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndromePratibha Bhalla, Qiumei Du, Ashwani Kumar, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|October 18, 2018
What's in a name? The heterogeneous clinical spectrum and prognostic factors in a cohort of adults with hemophagocytic lymphohistiocytosisBonnie C Prokesch, Srikanth Nagalla, Fatemeh Ezzati, et al.
Journal of Human Immunity|January 29, 2026
Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9<sup>+</sup> chondrocyte expansionPratibha Bhalla, Neha Ahuja, Ashwani Kumar, et al.
The Journal of Allergy and Clinical Immunology|February 7, 2013
Hypomorphic Janus kinase 3 mutations result in a spectrum of immune defects, including partial maternal T-cell engraftmentFederica Cattaneo, Mike Recher, Stefania Masneri, et al.
Blood|August 6, 2017
Novel nonsense gain-of-function <i>NFKB2</i> mutations associated with a combined immunodeficiency phenotypeHye Sun Kuehn, Julie E Niemela, Karthik Sreedhara, et al.
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