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An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature.
- Published in:
- Case Reports in Immunology, 2020, p. 1, doi. 10.1155/2020/8891902
- By:
- Publication type:
- Article
Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy.
- Published in:
- Case Reports in Immunology, 2019, p. 1, doi. 10.1155/2019/1902817
- By:
- Publication type:
- Article
An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation.
- Published in:
- Case Reports in Immunology, 2018, p. 1, doi. 10.1155/2018/6897935
- By:
- Publication type:
- Article
Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish Child.
- Published in:
- Molecular Syndromology, 2023, v. 14, n. 6, p. 504, doi. 10.1159/000531408
- By:
- Publication type:
- Article
TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2018, v. 10, n. 3, p. 192
- By:
- Publication type:
- Article
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.
- Published in:
- Clinical & Experimental Medicine, 2009, v. 9, n. 4, p. 339, doi. 10.1007/s10238-009-0053-1
- By:
- Publication type:
- Article
Psychological burden of pediatric primary immunodeficiency.
- Published in:
- Pediatrics International, 2018, v. 60, n. 10, p. 911, doi. 10.1111/ped.13675
- By:
- Publication type:
- Article
Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients.
- Published in:
- International Journal of Immunopathology & Pharmacology, 2018, v. 32, p. 1, doi. 10.1177/2058738418779458
- By:
- Publication type:
- Article
Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children.
- Published in:
- 2017
- By:
- Publication type:
- Letter to the Editor
CD4<sup>+</sup>CD25<sup>+</sup>Foxp3<sup>+</sup> T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency.
- Published in:
- International Journal of Immunopathology & Pharmacology, 2016, v. 29, n. 2, p. 241, doi. 10.1177/0394632015617064
- By:
- Publication type:
- Article
Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience.
- Published in:
- Immunologic Research, 2024, v. 72, n. 2, p. 225, doi. 10.1007/s12026-023-09426-9
- By:
- Publication type:
- Article
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections.
- Published in:
- International Archives of Allergy & Immunology, 2024, v. 185, n. 4, p. 392, doi. 10.1159/000535258
- By:
- Publication type:
- Article
Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies.
- Published in:
- International Archives of Allergy & Immunology, 2024, v. 185, n. 4, p. 382, doi. 10.1159/000534900
- By:
- Publication type:
- Article
Relapsing polychondritis in a child with common variable immunodeficiency.
- Published in:
- International Journal of Dermatology, 2009, v. 48, n. 5, p. 525, doi. 10.1111/j.1365-4632.2009.03809.x
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- Publication type:
- Article
Alterations in B and NK cells highly correlate with disease severity in children with COVID-19.
- Published in:
- Turkish Journal of Medical Sciences, 2023, v. 53, n. 5, p. 1205, doi. 10.55730/1300-0144.5686
- By:
- Publication type:
- Article
Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?
- Published in:
- Pediatric Reports, 2013, v. 5, n. 3, p. 53, doi. 10.4081/pr.2013.e14
- By:
- Publication type:
- Article
Çocuklarda sık yineleyen enfeksiyonlar, nörolojik bulgular, serum ürik asit düşüklüğü ve lenfopeni: Pürin nükleozid fosforilaz eksikliği, çocukluk çağı acil hastalıklarından biri.
- Published in:
- Türk Pediatri Arşivi, 2020, v. 55, n. 3, p. 320, doi. 10.14744/TurkPediatriArs.2019.83788
- By:
- Publication type:
- Article
Birincil immün yetersizliklerde, Mycobacterium Bovis ve mikobakterilerin sıklığı.
- Published in:
- Türk Pediatri Arşivi, 2017, v. 52, n. 3, p. 138, doi. 10.5152/TurkPediatriArs.2017.5240
- By:
- Publication type:
- Article
An unusual manifestation: Papillary thyroid carcinoma in a patient with ataxia-telengiectasia.
- Published in:
- Turkish Journal of Pediatrics, 2016, v. 58, n. 4, p. 442, doi. 10.24953/turkjped.2016.04.018
- By:
- Publication type:
- Article
Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings.
- Published in:
- Turkish Journal of Pediatrics, 2010, v. 52, n. 1, p. 89
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- Publication type:
- Article
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference.
- Published in:
- Clinical Case Reports, 2021, v. 9, n. 4, p. 2023, doi. 10.1002/ccr3.3934
- By:
- Publication type:
- Article
NEMO Mutasyonlu Bir Bebekten İzole Edilen Rifampisine Dirençli Mycobacterium bovis BCG Suşu.
- Published in:
- Bulletin of Microbiology / Mikrobiyoloji Bulteni, 2015, v. 49, n. 2, p. 272, doi. 10.5578/mb.8779
- By:
- Publication type:
- Article
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic Dermatitis.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 8, p. 1882, doi. 10.1007/s10875-023-01554-z
- By:
- Publication type:
- Article
Consanguinity Rate and Delay in Diagnosis in Turkish Patients with Combined Immunodeficiencies: a Single-Center Study.
- Published in:
- Journal of Clinical Immunology, 2011, v. 31, n. 1, p. 106, doi. 10.1007/s10875-010-9472-8
- By:
- Publication type:
- Article
Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections.
- Published in:
- Asian Pacific Journal of Allergy & Immunology, 2015, v. 33, n. 4, p. 312, doi. 10.12932/AP0586.33.4.2015
- By:
- Publication type:
- Article
Clinical and Laboratory Evaluation of Periodically Monitored Turkish Children with IgG Subclass Deficiencies.
- Published in:
- Asian Pacific Journal of Allergy & Immunology, 2009, v. 27, n. 1, p. 43
- By:
- Publication type:
- Article
Juvenile psoriatic arthritis carrying familial Mediterranean fever gene mutations in a 14-year-old Turkish girl.
- Published in:
- Journal of Dermatology, 2007, v. 34, n. 5, p. 344, doi. 10.1111/j.1346-8138.2007.00285.x
- By:
- Publication type:
- Article
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management.
- Published in:
- Allergologia & Immunopathologia, 2021, v. 49, n. 1, p. 95, doi. 10.15586/aei.v49i1.24
- By:
- Publication type:
- Article
Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients.
- Published in:
- Scandinavian Journal of Immunology, 2024, v. 99, n. 2, p. 1, doi. 10.1111/sji.13338
- By:
- Publication type:
- Article
Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency.
- Published in:
- Allergy, 2022, v. 77, n. 10, p. 3108, doi. 10.1111/all.15331
- By:
- Publication type:
- Article
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-08944-x
- By:
- Publication type:
- Article
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis.
- Published in:
- Molecular Biology Reports, 2023, v. 50, n. 1, p. 1, doi. 10.1007/s11033-023-08944-x
- By:
- Publication type:
- Article
Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review.
- Published in:
- Rheumatology International, 2020, v. 40, n. 1, p. 161, doi. 10.1007/s00296-019-04366-w
- By:
- Publication type:
- Article
Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients.
- Published in:
- Journal of Pediatric Research, 2024, v. 11, n. 2, p. 110, doi. 10.4274/jpr.galenos.2024.09735
- By:
- Publication type:
- Article
The Quality of Life and Mental Health in Children with Primary Immunodeficiency.
- Published in:
- Journal of Pediatric Research, 2019, v. 6, n. 1, p. 1, doi. 10.4274/jpr.galenos.2018.83097
- By:
- Publication type:
- Article
Konjenital Nötropenili On Çocukta Klinik, Laboratuvar ve Moleküler İncelemeler Desteğinde Tedavi ve Takibe Yaklaşım.
- Published in:
- Journal of Pediatric Research, 2016, v. 3, n. 1, p. 7, doi. 10.4274/jpr.19480
- By:
- Publication type:
- Article
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study.
- Published in:
- Pediatric Allergy & Immunology, 2020, v. 31, n. 5, p. 528, doi. 10.1111/pai.13231
- By:
- Publication type:
- Article
Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency.
- Published in:
- Pediatric Allergy & Immunology, 2007, v. 18, n. 2, p. 167, doi. 10.1111/j.1399-3038.2006.00491.x
- By:
- Publication type:
- Article
New Laboratory Findings in Turkish Patients with Transient Hypogammaglobulinemia of Infancy.
- Published in:
- Iranian Journal of Allergy, Asthma & Immunology, 2010, v. 9, n. 4, p. 237
- By:
- Publication type:
- Article
Immunodeficiency in a Child with Alström Syndrome.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia.
- Published in:
- Rheumatology International, 2006, v. 27, n. 2, p. 179, doi. 10.1007/s00296-006-0191-7
- By:
- Publication type:
- Article
Immunoglobin light chain levels can be used to determine disease stage in children with juvenile idiopathic arthritis.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
A clinical and laboratory approach to the evaluation of innate immunity in pediatric CVID patients.
- Published in:
- Frontiers in Immunology, 2015, v. 6, p. 1, doi. 10.3389/fimmu.2015.00145
- By:
- Publication type:
- Article