172 results on '"Tezcan, Ilhan"'
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2. Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway
3. COVID-19 Salgını Sırasında Doğuştan Bağışıklık Yetersizliği Olan Ergenlerde Psikososyal İşlevsellik
4. GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway
5. A large single‐center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey
6. Heterogeneity in RAG 1/2 Deficiency: 35 Cases From A Single Center
7. DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection
8. Cutaneous Findings in Inborn Errors of Immunity: An Immunologist`s Perspective
9. Hyper IgM Syndrome with a Novel Mutation in the AICDA Gene: Easy to Diagnose
10. Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III
11. Mutation in BTK Gene Causing an Atypical Presentation of XLA
12. A Patient Presenting with Chronic Mucocutaneous Candidiasis: A Novel IL12RB1 Mutation
13. Evaluation of periodontal status and cytokine response in children with familial Mediterranean fever or systemic juvenile idiopathic arthritis
14. Dental caries and associated salivary biomarkers in patients with cystic fibrosis
15. A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects
16. High Inborn Errors of Immunity Risk in Patients with Granuloma
17. Antimycobacterial prophylaxis regarding Bacillus Calmette-Guérin -associated complications in children with primary immunodeficiency
18. Childhood-onset Takayasu arteritis and immunodeficiency: case-based review
19. Recurrent Oral Aphtha, Diarrhea, Pneumonia, And Respiratory Distress Since Infancy: STAT1 GOF defect
20. First allogeneic hematopoietic stem cell transplantation in RASGRP1 deficiency: long-term follow-up
21. GIMAP6 regulates autophagy, immune competence, and inflammation in mice and humans
22. Evaluation of Health Status and Quality of Life in Patients Using Intravenous and Subcutaneous Forms of Immunoglobulin Replacement
23. Newborn Screening for SCID: The very first prospective pilot study from Turkey
24. Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients
25. Evaluation of the peripheral blood T and B cell subsets and IRF‐7 variants in adult patients with severe influenza virus infection
26. Cytokine profile in serum and gingival crevicular fluid of children with inflammatory bowel disease: A case‐control study
27. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)
28. Nutritional status of children with primary immunodeficiency: A single center experience
29. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature
30. Respiratory system findings in pediatric patients with primary immunodeficiency
31. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)
32. TMC8 mutation in a Turkish family with epidermodysplasia verruciformis including laryngeal papilloma and recurrent skin carcinoma
33. Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey
34. Differential diagnosis of primary immunodeficiency in patients with BCGitis and BCGosis: A single‐centre study
35. COVID-19 in Patients with Primary Immunodeficiency
36. Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
37. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X–linked Thrombocytopenia–A single center study
38. A Novel IL17RA Mutation In A Male Child With Chronic Mucocutaneous Candidiasis
39. Expression of HLA class I and class II genes in patients with multiple skin warts
40. Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency
41. Selective IgM deficiency: Follow‐up and outcome
42. Clinical and Laboratory Findings in Patients with Leukocyte Adhesion Deficiency Type I: A Multicenter Study in Turkey
43. The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease
44. Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience
45. COVID 19 in Patients With Primary Immunodeficiency
46. Long Term Follow-Up of the Patients with Severe Combined Immunodeficiency After Hematopoietic Stem Cell Transplantation: A Single-Center Study
47. A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess
48. Hematopoietic stem cell transplantation complicated with ebv associated hemophagocytic lymphohistiocytosis in a patient with dock2 deficiency
49. A RARE INVOLVEMENT OF CENTRAL NERVOUS SYSTEM INVOLVEMENT DUE TO CTLA-4 GENE DEFECT
50. Flow Cytometric Analysis of T Cell Vβ Repertoire in Common Variable Immunodeficiency Patients with TACI Mutations
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