Detalhe da pesquisa
1.
Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity.
Blood
; 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38579284
2.
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
3.
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
4.
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
5.
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic Dermatitis.
J Clin Immunol
; 43(8): 1882-1890, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37507632
6.
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
7.
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
8.
Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations.
Indian J Clin Biochem
; 38(4): 475-484, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37746537
9.
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.
Clin Immunol
; 244: 109131, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36179983
10.
Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulation.
J Autoimmun
; 132: 102891, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36113303
11.
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
12.
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
13.
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
14.
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
15.
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
16.
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.
J Allergy Clin Immunol
; 145(5): 1452-1463, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31887391
17.
Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.
Blood
; 141(26): 3226-3230, 2023 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36745868
18.
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
19.
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
20.
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