Detalhe da pesquisa
1.
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency.
Eur J Immunol
; 52(7): 1171-1189, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35562849
2.
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients.
J Clin Immunol
; 42(1): 130-145, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34664192
3.
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies.
J Immunol
; 205(11): 2979-2987, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33115853
4.
Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia.
Clin Immunol
; 230: 108802, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34298181
5.
NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential.
Clin Immunol
; 210: 108309, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31751612
6.
Regulation of Kit Expression in Early Mouse Embryos and ES Cells.
Stem Cells
; 37(3): 332-344, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566254
7.
Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells.
Int J Mol Sci
; 21(22)2020 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33203071
8.
Increased proportions of γδ T lymphocytes in atypical SCID associate with disease manifestations.
Clin Immunol
; 201: 30-34, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30776520
9.
Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child With Intermittent Neutropenia.
J Pediatr Hematol Oncol
; 41(4): e266-e269, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30044346
10.
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children.
Eur J Pediatr
; 178(1): 51-60, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30269248
11.
Impaired X-CGD T cell compartment is gp91phox-NADPH oxidase independent.
Clin Immunol
; 193: 52-59, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29410324
12.
A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.
J Allergy Clin Immunol
; 139(4): 1302-1310.e4, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27658761
13.
The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment.
Clin Immunol
; 178: 20-28, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26732860
14.
Agammaglobulinemia associated to nasal polyposis due to a hypomorphic RAG1 mutation in a 12 years old boy.
Clin Immunol
; 173: 121-123, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27713031
15.
Defective B-cell proliferation and maintenance of long-term memory in patients with chronic granulomatous disease.
J Allergy Clin Immunol
; 135(3): 753-61.e2, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25175493
16.
Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency.
J Clin Immunol
; 35(4): 373-83, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25875698
17.
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood.
J Clin Med
; 12(13)2023 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37445241
18.
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.
J Exp Med
; 220(5)2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36884218
19.
Severe Toxoplasma gondii infection in a member of a NFKB2-deficient family with T and B cell dysfunction.
Clin Immunol
; 183: 273-277, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28919517
20.
Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection.
J Clin Immunol
; 37(1): 32-35, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27770395