Detalhe da pesquisa
1.
Actin polymerisation after FCγR stimulation of human fibroblasts is BCL10 independent.
Clin Immunol
; 163: 120-2, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26774590
2.
Genetic errors of the human caspase recruitment domain-B-cell lymphoma 10-mucosa-associated lymphoid tissue lymphoma-translocation gene 1 (CBM) complex: Molecular, immunologic, and clinical heterogeneity.
J Allergy Clin Immunol
; 136(5): 1139-49, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26277595
3.
New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy.
J Allergy Clin Immunol
; 141(5): 1924-1927.e18, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29408330
4.
Clinical Features Before Hematopoietic Stem Cell Transplantation or Enzyme Replacement Therapy of Children With Combined Immunodeficiency.
Pediatr Infect Dis J
; 35(7): 794-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27078120
5.
Chronic granulomatous disease caused by maternal uniparental isodisomy of chromosome 16.
J Allergy Clin Immunol Pract
; 5(4): 1146-1148, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28341171
6.
A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.
J Allergy Clin Immunol
; 116(3): 690-7, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16159644
7.
Kinase activity and XLA phenotypic variability.
J Allergy Clin Immunol
; 115(1): 205-6, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15637572