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Rapid Drug Desensitization and Management of Breakthrough Reactions in Pediatric Patients.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2024, v. 22, n. 2, p. 170, doi. 10.21911/aai.2024.579
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- Publication type:
- Article
Diverse Clinical and Immunological Profiles in Patients with IPEX Syndrome: a Multicenter Analysis from Turkey.
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- Journal of Clinical Immunology, 2025, v. 45, n. 1, p. 1, doi. 10.1007/s10875-024-01791-w
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- Article
Interferon Gamma in Sickness Predisposing to Mycobacterial Infectious Diseases.
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- Balkan Medical Journal, 2024, v. 41, n. 5, p. 326, doi. 10.4274/balkanmedj.galenos.2024.2024-8-18
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- Article
Food-induced anaphylaxis in early childhood and factors associated with its severity.
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- Allergy & Asthma Proceedings, 2021, v. 42, n. 5, p. e135, doi. 10.2500/aap.2021.42.210051
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- Publication type:
- Article
Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children.
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- Pediatric Nephrology, 2023, v. 38, n. 7, p. 2199, doi. 10.1007/s00467-022-05813-w
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- Publication type:
- Article
Primary catastrophic antiphospholipid syndrome in an 8 year-old-girl.
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- Marmara Medical Journal, 2016, v. 29, n. 1, p. 41, doi. 10.5472/MMJcr.2901.07
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- Article
Perioperative hypersensitivity in children: A prospective multidisciplinary study.
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- Acta Anaesthesiologica Scandinavica, 2024, v. 68, n. 3, p. 321, doi. 10.1111/aas.14354
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- Article
Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency.
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- Allergy, 2022, v. 77, n. 10, p. 3108, doi. 10.1111/all.15331
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- Publication type:
- Article
Evolution and long‐term outcomes of combined immunodeficiency due to CARMIL2 deficiency.
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- Allergy, 2022, v. 77, n. 3, p. 1004, doi. 10.1111/all.15010
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- Article
Adverse COVID‐19 outcomes in immune deficiencies: Inequality exists between subclasses.
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- Allergy, 2022, v. 77, n. 1, p. 282, doi. 10.1111/all.15025
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- Publication type:
- Article
TNFRSF13B VARIANTS ACT AS MODIFIERS TO CLINICAL PHENOTYPES IN COMMON VARIABLE IMMUNE DEFICIENCY DISORDERS.
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- Journal of Advanced Research in Health Sciences (JARHS) / Sağlık Bilimlerinde İleri Araştırmalar Dergisi (SABİAD), 2023, v. 6, n. 3, p. 210, doi. 10.26650/JARHS2023-1346155
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- Publication type:
- Article
GENETIC AND CLINICAL PROFILING OF MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE PATIENTS; SINGLECENTER EXPERIENCE.
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- Journal of Advanced Research in Health Sciences (JARHS) / Sağlık Bilimlerinde İleri Araştırmalar Dergisi (SABİAD), 2022, v. 5, n. 3, p. 140, doi. 10.26650/JARHS2022-1119899
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- Publication type:
- Article
Evaluation of pediatric patients with suspected polyethylene glycol and polysorbate allergy before mRNA SARS-CoV2 vaccination.
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- Allergologia & Immunopathologia, 2023, v. 51, n. 3, p. 174, doi. 10.15586/aei.v51i3.800
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- Publication type:
- Article
STAT1/STAT3 Gain of Function and Mechanisms of Immune Dysregulation.
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- Turkish Journal of Immunology, 2024, v. 12, p. 47, doi. 10.4274/tji.galenos.2023.52386
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- Publication type:
- Article
DOCK8 Protein Eksikliğinin Saptanmasında Akan Hücre Ölçerin Tanısal Değeri.
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- Turkish Journal of Immunology, 2019, v. 7, n. 2, p. 102, doi. 10.25002/tji.2019.1109
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- Article
Kronik Granülomatöz Hastalarında ve Bu Hastalığı Genetik Olarak Taşıyan Bireylerde Lenfosit Fonksiyonları.
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- Turkish Journal of Immunology, 2019, v. 7, n. 2, p. 93, doi. 10.25002/tji.2019.1111
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- Publication type:
- Article
Basophil activation test is reliable for inhalant allergens in pediatric patients.
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- Turkish Journal of Immunology, 2016, v. 4, p. 65
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- Publication type:
- Article
Intracellular staining of DOCK8, LRBA, SAP and XIAP proteins by flow cytometry; Marmara experience.
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- Turkish Journal of Immunology, 2016, v. 4, p. 65
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- Publication type:
- Article
Detection of genetic variations in severe combined immunodeficiency (SCID) patients by targeted amplicon sequencing.
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- Turkish Journal of Immunology, 2016, v. 4, p. 64
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- Article
The distribution of NK subsets in CVID and some primary immunodeficient patients.
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- Turkish Journal of Immunology, 2016, v. 4, p. 48
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- Publication type:
- Article
Alerji öyküsü olan çocuklarda aşılama pratikleri.
- Published in:
- Türk Pediatri Arşivi, 2020, v. 55, n. 3, p. 244, doi. 10.14744/TurkPediatriArs.2020.96636
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- Publication type:
- Article
Birincil immün yetersizlikli hastalarda otoimmünite çeşitliliği, klinik özellikleri ve tedavi seçenekleri.
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- Türk Pediatri Arşivi, 2016, v. 51, n. 4, p. 186, doi. 10.5152/TurkPediatriArs.2016.3928
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- Publication type:
- Article
Birincil immün yetmezliklerde deri altı immünglobulin kullanımı.
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- Türk Pediatri Arşivi, 2016, v. 51, n. 1, p. 8, doi. 10.5152/TurkPediatriArs.2016.3058
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- Publication type:
- Article
Profile of the patients who present to immunology outpatient clinics because of frequent infections.
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- Türk Pediatri Arşivi, 2014, v. 49, n. 3, p. 210, doi. 10.5152/tpa.2014.1810
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- Article
Comparison oí oral microflora in seiective IgA deficiency and X linked agammaglobulinemia cases with control group.
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- 2013
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- Publication type:
- Journal Article
Selektif IgA eksikliği ve X’e bağlı agammaglobülinemi olgularında ağız mikroflorasının sağlam grupla karşılaştırılması.
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- Türk Pediatri Arşivi, 2013, v. 48, n. 3, p. 204, doi. 10.4274/tpa.438
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- Article
The phenotype-genotype relationship in severe congenital neutropenia patients.
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- 2012
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- Publication type:
- Journal Article
Doğuştan ağır nötropenide fenotip-genotip ilişkisi.
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- Türk Pediatri Arşivi, 2012, v. 47, n. 4, p. 272, doi. 10.4274/tpa.822
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- Publication type:
- Article
Mutational landscape of severe combined immunodeficiency patients from Turkey.
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- International Journal of Immunogenetics, 2020, v. 47, n. 6, p. 529, doi. 10.1111/iji.12496
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- Publication type:
- Article
A rare cause of severe superficial herpetic skin infection in a 13-month-old female patient: Autosomal recessive HIES.
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- 2018
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- Publication type:
- Case Study
Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections.
- Published in:
- Clinical & Experimental Neuroimmunology, 2016, v. 7, n. 1, p. 79, doi. 10.1111/cen3.12254
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- Article
Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty.
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- Hormone Research in Paediatrics, 2020, v. 93, n. 1, p. 66, doi. 10.1159/000505329
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- Publication type:
- Article
IFN-γR1 (CD119) ve IL-12Rβ1 (CD212) Eksikliğinin Akan Hücre Ölçer ile Analizi.
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- Bulletin of Microbiology / Mikrobiyoloji Bulteni, 2023, v. 57, n. 1, p. 83, doi. 10.5578/mb.20239907
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- Article
Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 5, p. 1036, doi. 10.1007/s10875-022-01262-0
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- Article
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.
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- 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
Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency.
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- Journal of Clinical Immunology, 2022, v. 42, n. 3, p. 582, doi. 10.1007/s10875-021-01176-3
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- Publication type:
- Article
Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency.
- Published in:
- 2021
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- Publication type:
- Letter
Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 1, p. 59, doi. 10.1007/s10875-020-00878-4
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- Publication type:
- Article
Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect.
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- Journal of Clinical Immunology, 2020, v. 40, n. 6, p. 883, doi. 10.1007/s10875-020-00816-4
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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
Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 1, p. 37, doi. 10.1007/s10875-018-0575-y
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- Publication type:
- Article
Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1.
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- Journal of Clinical Immunology, 2016, v. 36, n. 7, p. 641, doi. 10.1007/s10875-016-0312-3
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- Publication type:
- Article
Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.
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- Journal of Clinical Immunology, 2015, v. 35, n. 6, p. 523, doi. 10.1007/s10875-015-0178-9
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- Publication type:
- Article
Chronic Rhinosinusitis in Patients with Primary Immunodeficiency.
- Published in:
- International Archives of Allergy & Immunology, 2023, v. 184, n. 3, p. 302, doi. 10.1159/000527265
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- Publication type:
- Article
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease.
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- International Archives of Allergy & Immunology, 2020, v. 181, n. 7, p. 540, doi. 10.1159/000507366
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- Publication type:
- Article
Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency.
- Published in:
- International Archives of Allergy & Immunology, 2020, v. 181, n. 3, p. 228, doi. 10.1159/000504598
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- Publication type:
- Article
Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies.
- Published in:
- International Archives of Allergy & Immunology, 2019, v. 178, n. 1, p. 1, doi. 10.1159/000492824
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- Publication type:
- Article
Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?
- Published in:
- International Archives of Allergy & Immunology, 2017, v. 174, n. 1, p. 52, doi. 10.1159/000480082
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- Publication type:
- Article
Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: a single center experience.
- Published in:
- Turkish Journal of Pediatrics, 2020, v. 62, n. 3, p. 379, doi. 10.24953/turkjped.2020.03.004
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- Publication type:
- Article
Tanısı Oldukça Gecikmiş Bir İmmün Yetmezlik Olgusu: Good's Sendromu.
- Published in:
- Respiratory Case Reports, 2017, v. 6, n. 1, p. 36, doi. 10.5505/respircase.2017.48243
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- Article