Detalhe da pesquisa
1.
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2.
Clin Genet
; 92(4): 380-387, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28128455
2.
B-cell subsets in patients with transient hypogammaglobulinemia of infancy, partial IgA deficiency, and selective IgM deficiency.
J Investig Allergol Clin Immunol
; 23(2): 94-100, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23654075
3.
Bacille Calmette-Guérin lymphadenitis and recurrent oral candidiasis in an infant with a new mutation leading to interleukin-12 receptor beta-1 deficiency.
J Investig Allergol Clin Immunol
; 21(5): 401-4, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21905505
4.
CD27 expression on lymphocyte and sCD27 levels in children with asthma.
Allergol Immunopathol (Madr)
; 38(6): 327-32, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20800938
5.
An intensive approach to the treatment of disseminated BCG infection in a SCID patient.
Bone Marrow Transplant
; 30(1): 45-7, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12105777
6.
An unusual clinical presentation: invasive Candida non-albicans infections in ataxia telangiectasia.
J Investig Allergol Clin Immunol
; 18(6): 488-90, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-19123448
7.
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.
Clin Genet
; 62(1): 84-8, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12123493
8.
Natural killer cell numbers and cytotoxic activity in pediatric Hodgkin disease.
Pediatr Hematol Oncol
; 17(2): 133-9, 2000 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10734655