Detalhe da pesquisa
1.
DNA replication-associated inborn errors of immunity.
J Allergy Clin Immunol
; 151(2): 345-360, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36395985
2.
Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
J Allergy Clin Immunol
; 152(1): 266-277, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36841265
3.
CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency.
J Clin Immunol
; 43(6): 1393-1402, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156988
4.
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease.
J Clin Immunol
; 42(8): 1638-1652, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35829840
5.
Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.
Cell Mol Immunol
; 20(1): 11-25, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36302985
6.
Insights From Early Clinical Trials Assessing Response to mRNA SARS-CoV-2 Vaccination in Immunocompromised Patients.
Front Immunol
; 13: 827242, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35309332
7.
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.
Front Immunol
; 13: 973543, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36203612
8.
Monogenic Adult-Onset Inborn Errors of Immunity.
Front Immunol
; 12: 753978, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34867986
9.
Unstable regulatory T cells, enriched for naïve and Nrp1neg cells, are purged after fate challenge.
Sci Immunol
; 6(61)2021 07 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34301799
10.
Increased IL-10-producing regulatory T cells are characteristic of severe cases of COVID-19.
Clin Transl Immunology
; 9(11): e1204, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33209300
11.
Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.
Cell Mol Immunol
; 20(1): 114, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36471115