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The Journal of Experimental Medicine|December 14, 2022
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiencyRomain Lévy, Florian Gothe, Mana Momenilandi, et al.
Frontiers in Immunology|July 28, 2017
Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined ImmunodeficiencyAnderson Dik Wai Luk, Pamela P Lee, Huawei Mao, et al.
The Journal of Allergy and Clinical Immunology. in Practice|July 13, 2024
Interleukin (IL)-1/IL-6-Inhibitor-Associated Drug Reaction With Eosinophilia and Systemic Symptoms (DReSS) in Systemic Inflammatory IllnessesVivian E Saper, Lu Tian, Ruud H J Verstegen, et al.
Frontiers in Immunology|July 25, 2022
Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of ImmunityKoon-Wing Chan, Chung-Yin Wong, Daniel Leung, et al.
Cell Reports. Medicine|September 19, 2025
Global, regional, and national burden of headache disorders, 1990-2021, with forecasts to 2050: A Global Burden of Disease study 2021, Tissa Wijeratne, Jiyeon Oh, et al.
JAMA Neurology|May 23, 2025
Global, Regional, and National Burden of Nontraumatic Subarachnoid Hemorrhage: The Global Burden of Disease Study 2021, Ilari Rautalin, Victor Volovici, et al.
JAMA|July 29, 2026
Global Burden of Elevated LDL-C: Findings From the Global Burden of Disease Study 2023, Christian Razo, Nicole K DeCleene, et al.
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