Detalhe da pesquisa
1.
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections.
Int Arch Allergy Immunol
; 185(4): 392-401, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38154455
2.
Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies.
Int Arch Allergy Immunol
; 185(4): 382-391, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38246144
3.
Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency.
J Allergy Clin Immunol
; 152(6): 1634-1645, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595759
4.
Analysis of IL-1ß, TGF-ß, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis.
Mol Biol Rep
; 51(1): 15, 2023 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38085361
5.
Cardiac Assessment in Children with MIS-C: Late Magnetic Resonance Imaging Features.
Pediatr Cardiol
; 44(1): 44-53, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35916926
6.
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature.
Asian Pac J Allergy Immunol
; 41(4): 372-378, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33638623
7.
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants.
Scand J Immunol
; 95(6): e13163, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35303369
8.
Immunologic changes during desensitization with cow's milk: How it differs from natural tolerance or nonallergic state?
Ann Allergy Asthma Immunol
; 129(6): 751-757.e3, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35914664
9.
A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia.
J Pediatr Hematol Oncol
; 43(6): e780-e784, 2021 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33843817
10.
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management.
Allergol Immunopathol (Madr)
; 49(1): 95-100, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33528935
11.
Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation.
Pediatr Hematol Oncol
; 38(8): 745-752, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33966600
12.
Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation.
J Clin Immunol
; 40(4): 646, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32367426
13.
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients.
Allergy
; 75(4): 921-932, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31596517
14.
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study.
Pediatr Allergy Immunol
; 31(5): 528-536, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32060950
15.
Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review.
Rheumatol Int
; 40(1): 161-168, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31273456
16.
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages.
Scand J Immunol
; 89(2): e12737, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30506560
17.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev
; 264(1): 103-20, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25703555
18.
Anti-ß2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders.
Indian J Clin Biochem
; 34(1): 95-100, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30728679
19.
In vitro T lymphocyte proliferation by carboxyfluorescein diacetate succinimidyl ester method is helpful in diagnosing and managing primary immunodeficiencies.
J Clin Lab Anal
; 32(1)2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28383134
20.
Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant.
J Allergy Clin Immunol
; 147(2): 775-778.e8, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32858082