Detalhe da pesquisa
1.
Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria.
Cell;
183(7): 1826-1847.e31, 2020 12 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33296702
2.
Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency.
Nat Immunol;
19(9): 973-985, 2018 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30127434
3.
[Cystic fibrosis in Morroco : what do words mean without action ?] / Mucoviscidose au Maroc : que valent les mots sans les actes ?
Rev Med Liege;
79(3): 175-180, 2024 Mar.
Artigo
em Francês
| MEDLINE
| ID: mdl-38487912
4.
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
J Clin Immunol;
42(7): 1508-1520, 2022 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36198931
5.
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol;
42(7): 1473-1507, 2022 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35748970
6.
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee.
J Clin Immunol;
41(3): 666-679, 2021 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33598806
7.
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity.
J Clin Immunol;
41(6): 1339-1351, 2021 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34052995
8.
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol;
40(1): 65, 2020 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32086639
9.
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
J Clin Immunol;
40(1): 66-81, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32048120
10.
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol;
40(1): 24-64, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31953710
11.
Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families.
J Clin Immunol;
40(1): 96-104, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31696364
12.
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency.
Blood;
132(22): 2362-2374, 2018 11 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30254128
13.
IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis.
J Allergy Clin Immunol;
143(6): 2215-2226.e7, 2019 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30578871
14.
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.
Proc Natl Acad Sci U S A;
113(24): 6713-8, 2016 06 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27247391
15.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev;
264(1): 103-20, 2015 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25703555
16.
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
J Clin Immunol;
38(1): 129-143, 2018 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29226301
17.
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity.
J Clin Immunol;
38(1): 96-128, 2018 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29226302
18.
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
Blood;
127(25): 3154-64, 2016 06 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27114460
19.
Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants.
J Allergy Clin Immunol;
140(1): 232-241, 2017 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28011069
20.
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies.
J Allergy Clin Immunol;
136(4): 993-1006.e1, 2015 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26162572