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2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

3. The musculoskeletal system manifestations in children with familial Mediterranean fever

4. The origin of SARS-CoV-2 in Istanbul: Sequencing findings from the epicenter of the pandemic in Turkey

5. IFN-γR1 (CD119) ve IL-12Rβ1 (CD212) Eksikliğinin Akan Hücre Ölçer ile Analizi

7. Familial early-onset obesity in Turkish children: variants and polymorphisms in the melanocortin-4 receptor (MC4R) gene

8. Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

9. Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

10. Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C , and CALM1

11. Investigation of association between ABO blood groups and COVID-19 clinical severity

13. Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

14. Clinical evaluation of torpedo maculopathy in an infant population with additional genetic testing for NEXMIF mutation

15. Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

16. MİKOBAKTERİYEL HASTALIKLARA MENDEL DUYARLILIĞI HASTALARININ GENETİK VE KLİNİK PROFİLİ; TEK MERKEZ DENEYİMİ

17. Johanson–Blizzard's Syndrome with a Novel UBR1 Mutation

18. Genetic panel screening in patients with clinically unclassified systemic autoinflammatory diseases

19. The origin of SARS-CoV-2 in Istanbul: Sequencing findings from the epicenter of the pandemic in Turkey

20. Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

21. A boy with a novel homozygous ZAP70 mutation presenting with a dermatological phenotype and postnatal decrease in CD8 + T cells

22. Author response for 'A boy with a novel homozygous ZAP70 mutation presenting with a dermatological phenotype and postnatal decrease in CD8 + T cells'

23. Steroid hormone profiles and molecular diagnostic tools in pediatric patients with non-CAH primary adrenal insufficiency

24. Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency

25. Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

26. Impaired IL-23-dependent induction of IFN-gamma underlies mycobacterial disease in patients with inherited TYK2 deficiency

28. A Patient With Novel Icos Mutation Presented With Progressive Loss Of B Cells

29. Genomic Diversity of the SARS-CoV-2 in Turkey and the Impact of Virus Genome Mutations on Clinical Outcomes

30. Parents of ataxia-telangiectasia patients display a distinct cellular immune phenotype mimickingATM-mutated patients

31. Comparison of the clinical diagnostic criteria and the results of the next-generation sequence gene panel in patients with monogenic systemic autoinflammatory diseases

32. Does sampling saliva increase detection of SARS-CoV-2 by RT-PCR? Comparing saliva with oro-nasopharyngeal swabs

33. Author response for 'Parents of ataxia‐telangiectasia patients display a distinct cellular immune phenotype mimicking ATM mutated patients'

34. COVID-19 PCR Test Performance for Samples Stored at Ambient Temperature

35. COVID-19 PCR test performance on samples stored at ambient temperature

36. Responding to COVID-19 in Istanbul: Perspective from genomic laboratory

37. The Musculoskeletal System Manifestations in Children with Familial Mediterranean Fever

38. ADA2 Deficiency: Case Series of Five Patients with Varying Phenotypes

39. Does sampling saliva increase detection of SARS-CoV-2 by RT-PCR? Comparing saliva with oro-nasopharyngeal swabs

40. Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall–Stickler syndrome spectrum

41. A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation

42. Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2

44. Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability

45. Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

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