Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
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
6.
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
7.
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
8.
Psychological burden of pediatric primary immunodeficiency.
Pediatr Int
; 60(10): 911-917, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30103264
9.
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
10.
Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections.
Asian Pac J Allergy Immunol
; 33(4): 312-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26708396
11.
Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience.
Immunol Res
; 72(2): 225-233, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37840117
12.
The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study.
J Clin Immunol
; 33(1): 74-83, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22983506
13.
Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.
Eur J Pediatr
; 170(8): 1039-47, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21274562
14.
Erratum: X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up.
Am J Clin Exp Immunol
; 10(2): 63-64, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34584779
15.
Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants.
Turk Pediatri Ars
; 55(3): 320-327, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33061764
16.
Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.
Asian Pac J Allergy Immunol
; 27(1): 43-8, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19548629
17.
Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency.
J Allergy Clin Immunol Pract
; 7(8): 2790-2800.e15, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31238161
18.
An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation.
Case Reports Immunol
; 2018: 6897935, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30405923
19.
TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency.
Avicenna J Med Biotechnol
; 10(3): 192-195, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30090215
20.
Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients.
Int J Immunopathol Pharmacol
; 32: 2058738418779458, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29978731