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Risk factors predisposing children to food allergies.
- Published in:
- Allergologia & Immunopathologia, 2023, v. 51, n. 5, p. 72, doi. 10.15586/aei.v51i5.937
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- Publication type:
- Article
Tanınız nedir?
- Published in:
- Archives of the Turkish Dermatology & Venerology / Turkderm, 2014, v. 48, n. 4, p. 263
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- Publication type:
- Article
Investigation of causative genetic defects in patients with primary immunodefciency by next generation sequencing.
- Published in:
- Annals of Medical of Research, 2021, v. 28, n. 5, p. 1038, doi. 10.5455/annalsmedres.2021.03.201
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- Publication type:
- Article
Kronik Parotit: HIV-Enfekte Çocuk Hastanın İlk Bulgusu.
- Published in:
- Medical Journal of Bakirkoy, 2016, v. 12, n. 3, p. 140, doi. 10.5350/BTDMJB201612307
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- Publication type:
- Article
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 3, p. 634, doi. 10.1007/s10875-021-01191-4
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- Publication type:
- Article
A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
- Published in:
- 2019
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- Publication type:
- Letter
Novel Mutation in <italic>CECR1</italic> Leads to Deficiency of ADA2 with Associated Neutropenia.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 3, p. 273, doi. 10.1007/s10875-018-0487-x
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- Publication type:
- Article
Proven Food-Induced Acute Urticaria and Predictive Factors for Definitive Diagnosis in Childhood.
- Published in:
- International Archives of Allergy & Immunology, 2021, v. 182, n. 7, p. 607, doi. 10.1159/000513267
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- Publication type:
- Article
A rare case of syndromic severe congenital neutropenia: JAGN1 mutation.
- Published in:
- Turkish Journal of Pediatrics, 2020, v. 62, n. 2, p. 326, doi. 10.24953/turkjped.2020.02.022
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- Publication type:
- Article
Coexistence of early onset sarcoidosis and partial interferon-γ receptor 1 deficiency.
- Published in:
- Turkish Journal of Pediatrics, 2017, v. 58, n. 5, p. 545
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- Publication type:
- Article
Systemic onset juvenile idiopathic arthritis with macrophage activation syndrome and coronary artery dilatation misdiagnosed as Kawasaki disease.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 5, p. 518
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- Publication type:
- Article
Serum Magnesium Concentration in Children with Asthma.
- Published in:
- Eurasian Journal of Pulmonology, 2014, v. 16, n. 1, p. 36, doi. 10.5152/solunum.2014.25993
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- Publication type:
- Article
A Rare Cause of Congenital Neutropenia: SRP54 Variant.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2023, v. 21, n. 2, p. 156, doi. 10.21911/aai.122
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- Publication type:
- Article
DRESS Syndrome due to Carbamazepine Use in A Drug-Addicted Adolescent.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2023, v. 21, n. 1, p. 72, doi. 10.21911/aai.004
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- Publication type:
- Article
Knowledge and Experiences of Grandmothers on Food Allergies in Children.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2020, v. 18, n. 3, p. 128, doi. 10.21911/aai.536
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- Publication type:
- Article
IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018524
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- Publication type:
- Article
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants.
- Published in:
- Scandinavian Journal of Immunology, 2022, v. 95, n. 6, p. 1, doi. 10.1111/sji.13163
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- Publication type:
- Article
ITK Deficiency: How can EBV be Treated Before Lymphoma?
- Published in:
- 2015
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- Publication type:
- case study
Dupilumab combined with a short-term narrowbandultraviolet B phototherapy in a pediatric case of severe atopic dermatitis.
- Published in:
- Turkderm - Turkish Archives of Dermatology & Venereology, 2022, v. 56, n. 1, p. 39, doi. 10.4274/turkderm.galenos.2021.67424
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- Publication type:
- Article
A Case Diagnosed with Chronic Granulomatous Disease Presenting with Dactylitis.
- Published in:
- Bagcilar Medical Bulletin / Bağcılar Tıp Bülteni, 2024, v. 9, n. 1, p. 63, doi. 10.4274/BMB.galenos.2023.2023-08-070
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- Publication type:
- Article
The Course of COVID-19 in a Patient with Congenital Neutropenia: A Case Report.
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- Bagcilar Medical Bulletin / Bağcılar Tıp Bülteni, 2023, v. 8, n. 1, p. 94, doi. 10.4274/BMB.galenos.2022.2022-07-066
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- Publication type:
- Article
Bruton's Tyrosine Kinase Gene Mutations in Turkish Patients with X-Linked Agammaglobulinemia from a Single Center: Novel Mutations in βTK Gene.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2013, v. 33, n. 4, p. 1042, doi. 10.5336/medsci.2012-32189
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- Publication type:
- Article
The Effect of Phototherapy on the Lymphocyte Subsets in Newborn.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2011, v. 31, n. 5, p. 1245, doi. 10.5336/medsci.2011-23229
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- Publication type:
- Article
The Effect of Phototherapy on the Lymphocyte Subsets in Newborn.
- Published in:
- Turkiye Klinikleri Journal of Medical Sciences, 2011, v. 31, n. 4, p. 1245, doi. 10.5336/medsci.2011-23229
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- Publication type:
- Article
A Rare Clinical Finding in Ataxia Telangiectasia: Granulomatous Skin Lesion.
- Published in:
- Turkish Archives of Pediatrics, 2024, v. 59, n. 3, p. 325, doi. 10.5152/TurkArchPediatr.2024.23283
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- Publication type:
- Article
Primary immunodeficiencies: HSCT experiences of a single center in Turkey.
- Published in:
- Pediatric Transplantation, 2021, v. 25, n. 7, p. 1, doi. 10.1111/petr.14063
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- Publication type:
- Article
Regression of Cardiac Rhabdomyomas in a Neonate after Everolimus Treatment.
- Published in:
- Case Reports in Pediatrics, 2016, p. 1, doi. 10.1155/2016/8712962
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- Publication type:
- Article
Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Familial Mediterranean Fever: Diagnosing as Early as 3 Months of Age.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
A novel homozygous frameshift CCNO variant presenting with primary ciliary dyskinesia and selective IgM deficiency.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 11, p. 3333, doi. 10.1002/ppul.26607
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- Publication type:
- Article
Comparison of Diagnostic Efficacy of Lancet, Multi-Head Applicator, and Specific Immunoglobulin E in Allergy Testing.
- Published in:
- Journal of the Child / Çocuk Dergisi, 2023, v. 23, n. 3, p. 53, doi. 10.26650/jchild.2023.1341124
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- Publication type:
- Article
Primer İmmun Yetersizliklerin Tanısında Farkındalığı Arttıracak Klinik Özelliklerin Değerlendirilmesi.
- Published in:
- Journal of the Child / Çocuk Dergisi, 2017, v. 17, n. 2, p. 67, doi. 10.5222/j.child.2017.067
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- Publication type:
- Article
Single Mutation Different Clinical Findings: IGLL1 Defect.
- Published in:
- 2024
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- Publication type:
- Case Study
HAX-1 deficiency: Characteristics of five cases including an asymptomatic patient.
- Published in:
- Asian Pacific Journal of Allergy & Immunology, 2016, v. 34, n. 1, p. 73, doi. 10.12932/ap0618.34.1.2016
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- Publication type:
- Article
Lovebird-induced Aspergillus Infection in a Child with Chronic Granulomatous Disease.
- Published in:
- Cam ve Sakura Medical Journal, 2022, v. 2, n. 2, p. 75, doi. 10.4274/csmedj.galenos.2022.2022-1-1
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- Publication type:
- Article
COCUK SAĞLIĞININ DUZENLİ İZLEMİ VE PRİMER İMMUN YETMEZLİK HASTALARININ ERKEN TANINABİLİRLİĞİ.
- Published in:
- Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2018, v. 81, n. 4, p. 145, doi. 10.26650/IUITFD.348181
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- Publication type:
- Article
Life quality, depression, and anxiety levels in parents of children with primary immunodeficiency.
- Published in:
- Pediatric Allergy & Immunology, 2024, v. 35, n. 1, p. 1, doi. 10.1111/pai.14068
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- Publication type:
- Article
Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 7, p. 1, doi. 10.1007/s10875-024-01759-w
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- Publication type:
- Article
A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 3, p. 1, doi. 10.1007/s10875-024-01675-z
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- Publication type:
- Article
Neurologic Status of Patients with Purine Nucleoside Phosphorylase Deficiency Before and After Hematopoetic Stem Cell Transplantation.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 8, p. 2062, doi. 10.1007/s10875-023-01585-6
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- Publication type:
- Article
Kawasaki disease presenting as meningitis in a two months old infant.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Paediatric Tuberculosis at a Referral Hospital in Istanbul: Analysis of 250 Cases.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/6896279
- By:
- Publication type:
- Article
Iliopsoas abscess in the neonate with immunodeficiency.
- Published in:
- Pediatrics International, 2012, v. 54, n. 3, p. 439, doi. 10.1111/j.1442-200X.2012.03623.x
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- Publication type:
- Article