130 results on '"Aksu, Güzide"'
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2. Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: A multicenter study
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3. Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients.
4. Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis
5. Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients
6. Alterations in B and NK cells highly correlate with disease severity in children with COVID-19
7. Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients.
8. Analysis of IL-1β, TGF- Β, Il-5, ACE and PTPN22 Gene Polymorphisms and GEN Expression Levels in Turkish Chlidren with IgA Vasculitis
9. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
10. 1051. Cardiac Assessment in Children with MIS-C: Late Magnetic Resonance Imaging Features
11. Fc Receptor–like Proteins (FCRL): Immunomodulators of B Cell Function
12. Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation inIL-21Rgene and successful treatment with hematopoietic stem cell transplantation
13. Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency
14. A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature
15. Autoantibody Positivity in Children with Chronic Diarrhea
16. Recurrent infections, neurologic signs, low serum uricacid levels, and lymphopenia in childhood: Purinenucleoside phosphorylase deficiency, an emergencyfor infants
17. Permanent neonatal diabetes with arthrSogryposis multiplex congenita and neurogenic bladder – a new syndrome?
18. Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation.
19. Prepubertal periodontitis associated with chronic granulomatous disease
20. The Quality of Life and Mental Health in Children with Primary Immunodeficiency
21. Effect of Short-term Probiotic Yogurt Consumption on Caries Risk Factors in Infants
22. Thymic output changes in children with clinical findings signaling a probable primary immunodeficiency
23. Çocuklarda sık yineleyen enfeksiyonlar, nörolojik bulgular, serum ürik asit düşüklüğü ve lenfopeni: Pürin nükleozid fosforilaz eksikliği, çocukluk çağı acil hastalıklarından biri.
24. Primer Biliyer Kolanjit ve Otoimmün Karaciğer Hastalıklarında Çölyak Hastalığı Prevalansı
25. An unusual manifestation: Papillary thyroid carcinoma in a patient with ataxia-telengiectasia
26. A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity
27. Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia
28. The demographic datas of chronic granulomatous disease patients and the comparation of the clinical datas before and after interferon-gamma treatment in our country
29. An unusual manifestation: papillary thyroid carcinoma in a patient with ataxia-telengiectasia
30. Birincil immün yetersizliklerde, Mycobacterium Bovis ve mikobakterilerin sıklığı.
31. Akut romatizmal ateşli hastalarda lenfosit alt grupları, aksesuar moleküller,CD95-Bcl-2 ve TGFBeta1 düzeylerinin klinik evrelerle ilişkisi
32. Fc Receptor–like Proteins (FCRL): Immunomodulators of B Cell Function
33. A Rare Presentation Of Ataxia Telangiectasia: Immunodeficiency With Monoclonal IgM Gammapathy
34. SIK GÖRÜLEN DEĞİŞKEN İMMUN YETERSİZLİK: OLGULARIN KLİNİK, LABORATUVAR VE İZLEM BULGULARININ DEĞERLENDİRİLMESİ
35. Konjenital Nötropenili On Çocukta Klinik, Laboratuvar ve Moleküler İncelemeler Desteğinde Tedavi ve Takibe Yaklaşım.
36. Evaluation of the immunomodulatory properties in mice and in vitro anti-inflammatory activity of cycloartane type saponins from Astragalus species
37. Major Histocompatibility Complex (MHC) II Deficiency Needs Early Stem Cell Transplantation: A Case Report
38. Fc Receptor-like Proteins (FCRL): Immunomodulators of B Cell Function.
39. Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: Expanding the phenotypic spectrum ofRab27Amutations in humans
40. Growth and Endocrine Dysfunction in Thalassemia Major
41. Juvenil dermatomyozit-skleroderma çakışma sendromlu olgu sunumu.
42. MYCOBACTERIUM FORTUITUM-CHELONAE COMPLEX INFECTION IN A CHILD WITH COMPLETE INTERLEUKIN-12 RECEPTOR BETA 1 DEFICIENCY
43. Evaluation of Transforming Growth Factor-β1 Level in Crevicular Fluid of Cyclosporin A-Treated Patients
44. Mannose-binding lectin may affect pregnancy outcome.
45. Liver Histopathology in The Beta Thalassemic Patients
46. The Importance of IN VIVO and IN VITRO Technics With PPD For The Diagnosis of Childhood Tuberculosis
47. Umblical Cord Blood Collection Technics
48. The Safety And Effectiveness of Placental Blood For Autologous Transfusion
49. Ãlkemizde kronik granülomatöz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi öncesi ve sonrası klinik verilerinin karşılaştırılması.
50. lkemizde kronik granlomatz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi ncesi ve sonrası klinik verilerinin karşılaştırılması.
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