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UnknownManagement change following NGS diagnosis of inborn errors of immunity: The Australasian experience.
Not available
S-EPMC13629484 | biostudies-literature
UnknownHuman PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3Kδ syndrome 2.
Not available
S-EPMC10037341 | biostudies-literature
UnknownGenetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.
Not available
S-EPMC5187691 | biostudies-literature
UnknownRecessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.
Not available
S-EPMC9206114 | biostudies-literature
UnknownAutoantibodies against type I IFNs in patients with critical influenza pneumonia.
Not available
S-EPMC9485705 | biostudies-literature
UnknownRespiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
Not available
S-EPMC9178406 | biostudies-literature
UnknownRare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Not available
S-EPMC10074346 | biostudies-literature
UnknownX-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.
Not available
S-EPMC8532080 | biostudies-literature
UnknownInborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Not available
S-EPMC7857407 | biostudies-literature
UnknownThe risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies.
Not available
S-EPMC9173764 | biostudies-literature
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