Detalhe da pesquisa
1.
IL-4 receptor alpha blockade dampens allergic inflammation and upregulates IL-17A expression to promote Saureus clearance in antigen sensitized mouse skin.
J Allergy Clin Immunol
; 152(4): 907-915, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315811
2.
Efficacy and economics of targeted panel versus whole-exome sequencing in 878 patients with suspected primary immunodeficiency.
J Allergy Clin Immunol
; 147(2): 723-726, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32888943
3.
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2).
J Allergy Clin Immunol
; 145(6): 1664-1672.e10, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31945408
4.
T-cell mitochondrial dysfunction and lymphopenia in DOCK2-deficient patients.
J Allergy Clin Immunol
; 144(1): 306-309.e2, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30826364
5.
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.
J Allergy Clin Immunol
; 143(4): 1649-1653.e3, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30654050
6.
Rethinking newborn screening for severe combined immunodeficiency: Lessons from an international partnership for patients with primary immunodeficiencies in Pakistan.
Clin Immunol
; 202: 29-32, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30858051
7.
Immune dysregulation caused by homozygous mutations in CBLB.
J Clin Invest
; 132(20)2022 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36006710
8.
Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complex.
J Clin Invest
; 131(3)2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33529166
9.
Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2.
Turk J Pediatr
; 61(3): 413-417, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31916720