Detalhe da pesquisa
1.
A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis.
Clin Immunol
; 223: 108645, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33301882
2.
Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis.
J Clin Immunol
; 41(1): 59-65, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33025377
3.
Single-Center Study of 72 Patients with Severe Combined Immunodeficiency: Clinical and Laboratory Features and Outcomes.
J Clin Immunol
; 41(7): 1563-1573, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34114123
4.
Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature.
J Clin Immunol
; 40(3): 466-474, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32020378
5.
PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects.
J Allergy Clin Immunol
; 143(1): 325-334.e2, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29906526
6.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev
; 264(1): 103-20, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25703555
7.
Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia.
J Clin Immunol
; 38(3): 273-277, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29564582
8.
Cyclic manner of neutropenia in a patient with HAX-1 mutation.
Pediatr Hematol Oncol
; 35(3): 181-185, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30346863
9.
Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency.
J Clin Immunol
; 40(3): 539-542, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32016651
10.
Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants.
Immunol Res
; 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38644452
11.
HLA-haploidentical transplantations for primary immunodeficiencies: a single-center experience.
Pediatr Transplant
; 16(5): 451-7, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22594916
12.
ITK Deficiency: How can EBV be Treated Before Lymphoma?
Pediatr Blood Cancer
; 62(12): 2247-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26174447
13.
Late onset hemorrhagic cystitis in a hematopoietic stem cell recipient: treatment with intravesical hyaluronic acid.
Pediatr Transplant
; 14(6): E79-82, 2010 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19344339
14.
A rare case of syndromic severe congenital neutropenia: JAGN1 mutation.
Turk J Pediatr
; 62(2): 326-331, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32419428
15.
Evaluation of allergic sensitization and gastroesophageal reflux disease in children with recurrent croup.
Pediatr Int
; 51(5): 661-5, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19419517
16.
Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency.
Case Rep Pediatr
; 2014: 614238, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24511403
17.
CD40 ligand deficiency with grade III liver fibrosis, transplanted by a treosulphan-based conditioning regimen.
Exp Clin Transplant
; 9(5): 349-52, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21967264