Detalhe da pesquisa
1.
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2).
J Allergy Clin Immunol
; 145(6): 1664-1672.e10, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31945408
2.
Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activation.
J Allergy Clin Immunol
; 146(1): 192-202, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31862378
3.
DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
J Clin Immunol
; 37(8): 811-819, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29058101
4.
Detection of Sp110 by Flow Cytometry and Application to Screening Patients for Veno-occlusive Disease with Immunodeficiency.
J Clin Immunol
; 37(7): 707-714, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28825155
5.
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol
; 136(2): 402-12, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25724123
6.
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.
J Clin Immunol
; 35(2): 189-98, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25627830
7.
WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cells.
J Exp Med
; 204(2): 369-80, 2007 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-17296785
8.
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.
J Allergy Clin Immunol
; 124(6): 1289-302.e4, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20004785