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 gut mycobiota tune immunity via CARD9-dependent induction of anti-fungal IgG antibodies.
Cell
; 184(4): 1017-1031.e14, 2021 02 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33548172
3.
Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Cell
; 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38776920
4.
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
5.
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
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.
Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis.
J Clin Immunol
; 43(5): 921-932, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36821021
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.
CARD9 Expression Pattern, Gene Dosage, and Immunodeficiency Phenotype Revisited.
J Clin Immunol
; 42(2): 336-349, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34791587
11.
Functional analysis of two STAT1 gain-of-function mutations in two Iranian families with autosomal dominant chronic mucocutaneous candidiasis.
Med Mycol
; 59(2): 180-188, 2021 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32526033
12.
Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections.
J Clin Immunol
; 40(2): 359-366, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31940125
13.
Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome.
J Clin Immunol
; 40(6): 807-819, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32572726
14.
Delay in the Diagnosis of APECED: A Case Report and Review of Literature from Iran.
Immunol Invest
; 49(3): 299-306, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31588815
15.
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.
Proc Natl Acad Sci U S A
; 113(51): E8277-E8285, 2016 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27930337
16.
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency.
J Clin Immunol
; 38(5): 617-627, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29995221
17.
Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rß1 deficiencies.
Pediatr Blood Cancer
; 64(6)2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27873456
18.
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.
J Allergy Clin Immunol
; 138(1): 241-248.e3, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26936803
19.
Age-dependent association between pulmonary tuberculosis and common TOX variants in the 8q12-13 linkage region.
Am J Hum Genet
; 92(3): 407-14, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23415668
20.
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type Rash.
J Clin Immunol
; 41(3): 698-700, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33404972