Detalhe da pesquisa
1.
Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Cell;
187(2): 390-408.e23, 2024 01 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38157855
2.
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.
Cell;
186(3): 621-645.e33, 2023 02 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36736301
3.
Role of IL-27 in Epstein-Barr virus infection revealed by IL-27RA deficiency.
Nature;
628(8008): 620-629, 2024 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38509369
4.
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
Nature;
623(7988): 803-813, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37938781
5.
Human autoantibodies neutralizing type I IFNs: From 1981 to 2023.
Immunol Rev;
322(1): 98-112, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38193358
6.
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies.
Proc Natl Acad Sci U S A;
119(21): e2200413119, 2022 05 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35576468
7.
Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency.
J Clin Immunol;
44(3): 62, 2024 Feb 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38363432
8.
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.
Proc Natl Acad Sci U S A;
118(15)2021 04 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33876776
9.
Autoantibodies Neutralizing Type I IFNs in the Bronchoalveolar Lavage of at Least 10% of Patients During Life-Threatening COVID-19 Pneumonia.
J Clin Immunol;
43(6): 1093-1103, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37209324
10.
JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.
N Engl J Med;
382(3): 256-265, 2020 01 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31940699
11.
Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency.
J Immunol;
207(1): 133-152, 2021 07 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34183371
12.
Chronic Granulomatous Disease-Like Presentation of a Child with Autosomal Recessive PKCδ Deficiency.
J Clin Immunol;
42(6): 1244-1253, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35585372
13.
Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency.
J Clin Immunol;
42(5): 975-985, 2022 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35338423
14.
Lower disease activity but higher risk of severe COVID-19 and herpes zoster in patients with systemic lupus erythematosus with pre-existing autoantibodies neutralising IFN-α.
Ann Rheum Dis;
81(12): 1695-1703, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35973806
15.
Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance.
J Clin Immunol;
41(3): 639-657, 2021 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33417088
16.
JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study.
Rheumatology (Oxford);
60(12): 5801-5808, 2021 12 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33576769
17.
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.
Int Immunol;
32(10): 663-671, 2020 09 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32603428
18.
Impaired IL-12- and IL-23-Mediated Immunity Due to IL-12Rß1 Deficiency in Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease.
J Clin Immunol;
38(7): 787-793, 2018 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30255293
19.
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.
J Clin Immunol;
38(3): 278-282, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29589181
20.
Late-Onset EBV Susceptibility and Refractory Pure Red Cell Aplasia Revealing DADA2.
J Clin Immunol;
40(6): 948-953, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32643137