Detalhe da pesquisa
1.
Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity.
Haematologica
; 107(3): 765-769, 2022 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34854278
2.
CD160-associated CD8 T-cell functional impairment is independent of PD-1 expression.
PLoS Pathog
; 10(9): e1004380, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25255144
3.
Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Haematologica
; 97(9): 1312-9, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22491737
4.
Measurement of circulating CD21-CD27- B lymphocytes in SLE patients is associated with disease activity independently of conventional serological biomarkers.
Sci Rep
; 12(1): 9189, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35654865
5.
SLAMF Receptor Expression Identifies an Immune Signature That Characterizes Systemic Lupus Erythematosus.
Front Immunol
; 13: 843059, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35603218
6.
Restoration of NK Cell Cytotoxic Function With Elotuzumab and Daratumumab Promotes Elimination of Circulating Plasma Cells in Patients With SLE.
Front Immunol
; 12: 645478, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33828555
7.
Exhaustion of bacteria-specific CD4 T cells and microbial translocation in common variable immunodeficiency disorders.
J Exp Med
; 211(10): 2033-45, 2014 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-25225461
8.
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry.
Orphanet J Rare Dis
; 9: 183, 2014 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25491320
9.
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.
Blood
; 108(1): 346-52, 2006 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16537803