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Medrxiv : the Preprint Server for Health Sciences|June 19, 2023
Rethinking immunologic risk: a retrospective cohort study of severe SARS-CoV-2 infections in individuals with congenital immunodeficienciesAlan A Nguyen, Saddiq B Habiballah, Brenna LaBere, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 19, 2021
Ten Years of Newborn Screening for Severe Combined Immunodeficiency (SCID) in MassachusettsJaime E Hale, Craig D Platt, Francisco A Bonilla, et al.
Radiology|September 25, 2019
Simple Adnexal Cysts: SRU Consensus Conference Update on Follow-up and ReportingDeborah Levine, Maitray D Patel, Elizabeth J Suh-Burgmann, et al.
The Journal of Clinical Investigation|August 25, 2022
Immune dysregulation caused by homozygous mutations in CBLBErin Janssen, Zachary Peters, Mohammed F Alosaimi, et al.
Med (New York, N.Y.)|February 28, 2025
A progranulin variant causing childhood interstitial lung disease responsive to anti-TNF-α biologic therapyJohn C Kennedy, Sara O Vargas, Martha P Fishman, et al.
The Journal of Allergy and Clinical Immunology|February 4, 2026
A clinically validated assay for rapid determination of type I and type II interferon activity in systemic inflammatory diseasesMichael T Lam, Amrita Basu, Kailey E Brodeur, et al.
The New England Journal of Medicine|December 11, 2012
Chromosomal microarray versus karyotyping for prenatal diagnosisRonald J Wapner, Christa Lese Martin, Brynn Levy, et al.
The Journal of Clinical Investigation|February 2, 2021
Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complexWayne Bainter, Craig D Platt, Seung-Yeol Park, et al.
JCI Insight|August 24, 2018
Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in miceJianqiang Bao, Carlos J Perez, Jeesun Kim, et al.
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