Filter your results
- 2
- 2
- 4
- 4
- 2
- 1
- 1
- 4
- 4
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 4
- 3
- 3
- 3
- 3
- 3
- 3
- 3
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
|
|
sorted by
|
|
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory SyndromeJournal of Clinical Immunology, 2022, 42 (3), pp.471-483. ⟨10.1007/s10875-022-01215-7⟩
Journal articles
hal-03691612v1
|
||
|
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotesJournal of Experimental Medicine, 2022, 219 (6), pp.e20220028. ⟨10.1084/jem.20220028⟩
Journal articles
pasteur-03681917v1
|
||
|
Dominant-negative mutations in human IL6ST underlie hyper-IgE syndromeJournal of Experimental Medicine, 2020, 217 (6), ⟨10.1084/jem.20191804⟩
Journal articles
hal-02549533v1
|
||
|
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19Science Immunology, 2021, 6 (62), ⟨10.1126/sciimmunol.abl4348⟩
Journal articles
hal-03367639v1
|