Detalhe da pesquisa
1.
Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome.
Cent Eur J Immunol
; 48(3): 228-236, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37901871
2.
Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency.
Allergy
; 77(10): 3108-3123, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35491430
3.
Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function.
Blood
; 131(21): 2335-2344, 2018 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-29653965
4.
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients.
Allergy
; 75(4): 921-932, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31596517
5.
A Case of Ataxia-telangiectasia Presented With Hemophagocytic Syndrome.
J Pediatr Hematol Oncol
; 40(8): e547-e549, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29620677
6.
Hemophagocytic bone marrow aplasia with plasma cells in a RAG2-deficient SCID case after a nonconditioned transplantation from a fully matched sibling.
J Pediatr Hematol Oncol
; 35(8): e335-7, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23389499
7.
Validity of using pallor to detect children with mild anemia.
Pediatr Int
; 50(2): 232-4, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18353066