Detalhe da pesquisa
1.
Post-transplant monitoring of NK cell counts as a simple approach to predict the occurrence of opportunistic infection in liver transplant recipients.
Transpl Infect Dis
; 18(4): 552-65, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27260953
2.
Multicenter study for the evaluation of the antibody response against salmonella typhi Vi vaccination (EMPATHY) for the diagnosis of Anti-polysaccharide antibody production deficiency in patients with primary immunodeficiency.
Clin Immunol
; 169: 80-84, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236002
3.
Generation, establishment and characterization of a pluripotent stem cell line (CVTTHi001-A) from primary fibroblasts isolated from a patient with activated PI3 kinase delta syndrome (APDS2).
Stem Cell Res
; 49: 102082, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33221676
4.
Longitudinal analysis of immune function in the first 3 years of life in thymectomized neonates during cardiac surgery.
Clin Exp Immunol
; 154(3): 375-83, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18811694
5.
Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation.
Hum Mutat
; 17(2): 152-3, 2001 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11180601
6.
Herpes virus saimiri transformation of T cells in CD3 gamma immunodeficiency: phenotypic and functional characterization.
J Immunol Methods
; 198(2): 177-86, 1996 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-8946013
7.
New species-specific alleles at the primate MHC-G locus.
Hum Immunol
; 41(1): 52-5, 1994 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-7836065
8.
[Prenatal diagnosis and novel mutation in X-linked chronic granulomatous disease]. / Diagnóstico prenatal y nueva mutación en enfermedad granulomatosa crónica ligada al cromosoma X.
An Pediatr (Barc)
; 74(4): 261-5, 2011 Apr.
Artigo
em Espanhol
| MEDLINE | ID: mdl-21296630
9.
[Familial splenomegaly as a first clinical sign of autoimmune lymphoproliferative syndrome]. / Esplenomegalia familiar como manifestación clínica del síndrome linfoprolifetativo autoinmune.
An Pediatr (Barc)
; 72(4): 278-81, 2010 Apr.
Artigo
em Espanhol
| MEDLINE | ID: mdl-20227933
10.
Partial immune reconstitution after bone marrow transplantation in a boy with recombination activating gene 1 defect.
Bone Marrow Transplant
; 33(8): 877-8, 2004 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-14990985
11.
Retinol (vitamin A) is a cofactor in CD3-induced human T-lymphocyte activation.
Immunology
; 90(3): 388-96, 1997 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9155646
12.
Three new HLA-G alleles and their linkage disequilibria with HLA-A.
Immunogenetics
; 38(5): 323-31, 1993.
Artigo
em Inglês
| MEDLINE | ID: mdl-8102125
13.
Both morphological and molecular characters support speciation of South American siskins by sexual selection.
Cell Mol Life Sci
; 58(14): 2117-28, 2001 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11814061
14.
The evolution of the MHC-G gene does not support a functional role for the complete protein.
Immunol Rev
; 183: 65-75, 2001 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11782247
15.
The Old World sparrows (genus Passer) phylogeography and their relative abundance of nuclear mtDNA pseudogenes.
J Mol Evol
; 53(2): 144-54, 2001 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11479685
16.
Phylogeography of crossbills, bullfinches, grosbeaks, and rosefinches.
Cell Mol Life Sci
; 58(8): 1159-66, 2001 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-11529508
17.
Immunodeficiency associated with anorexia nervosa is secondary and improves after refeeding.
Immunology
; 94(4): 543-51, 1998 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-9767443
18.
A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: a possible CD2/lymphocyte function-associated antigen-1 functional association in humans.
Immunology
; 99(3): 440-50, 2000 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10712675
19.
Role of Nijmegen breakage syndrome protein in specific T-lymphocyte activation pathways.
Clin Diagn Lab Immunol
; 8(4): 757-61, 2001 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-11427422
20.
A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency.
Clin Diagn Lab Immunol
; 8(1): 133-7, 2001 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11139207