Detalhe da pesquisa
1.
The effects of video-assisted breastfeeding education given to primiparous pregnant women on breastfeeding self-efficacy: randomized control study.
BMC Pregnancy Childbirth
; 24(1): 142, 2024 Feb 17.
Artigo
Inglês
| MEDLINE | ID: mdl-38368316
2.
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
Inglês
| MEDLINE | ID: mdl-37595759
3.
Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1.
Clin Immunol
; 253: 109691, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37433423
4.
Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III.
J Clin Immunol
; 43(6): 1250-1258, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37014583
5.
Increased radiosensitivity and impaired DNA repair in patients with STAT3-LOF and ZNF341 deficiency, potentially contributing to malignant transformations.
Clin Exp Immunol
; 209(1): 83-89, 2022 07 22.
Artigo
Inglês
| MEDLINE | ID: mdl-35511492
6.
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency.
Blood
; 136(23): 2638-2655, 2020 12 03.
Artigo
Inglês
| MEDLINE | ID: mdl-32603431
7.
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
Inglês
| MEDLINE | ID: mdl-35491430
8.
Clinical Profile and Outcomes of Primary Immunodeficiency and Malignancy in Childhood at a Tertiary Oncology Center in Developing Country.
Pediatr Hematol Oncol
; 39(7): 600-612, 2022 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-35282762
9.
Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency.
J Clin Immunol
; 41(6): 1272-1290, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33929673
10.
Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis.
J Clin Immunol
; 41(8): 1804-1838, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34390440
11.
A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.
Hum Mol Genet
; 27(22): 3919-3935, 2018 11 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31222290
12.
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients.
Allergy
; 75(4): 921-932, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31596517
13.
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study.
Pediatr Allergy Immunol
; 31(5): 528-536, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32060950
14.
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Pediatr Blood Cancer
; 66(10): e27923, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31321910
15.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev
; 264(1): 103-20, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25703555
16.
Comparison of reference systems in the assessment of age-related serum immunoglobulin levels in pediatric patients
Turk J Med Sci
; 49(1): 147-152, 2019 Feb 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30764591
17.
Clinical characteristics of COVID-19 in children and young adolescents with inborn errors of immunity.
Pediatr Allergy Immunol
; 33(1): e13661, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34510555
18.
A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.
Hum Mol Genet
; 28(3): 524, 2019 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30329057
19.
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
J Allergy Clin Immunol
; 136(2): 402-12, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-25724123
20.
DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.
J Clin Immunol
; 35(2): 189-98, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25627830