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1. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.

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

3. The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

4. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

5. Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

6. From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio

9. Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

11. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

12. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

14. Author Correction: A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection (Nature Immunology, (2022), 23, 2, (159-164), 10.1038/s41590-021-01030-z)

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

16. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

17. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

19. SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

21. SARS-CoV-2-related MIS-C:A key to the viral and genetic causes of Kawasaki disease?

23. The genetic structure of the Turkish population reveals high levels of variation and admixture

26. Human CRY1 variants associate with attention deficit/hyperactivity disorder

28. Human CRY1 variants associate with attention deficit/hyperactivity disorder

36. Endothelial progenitor cells display clonal restriction in multiple myeloma

37. Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.

38. A retrospective comparison of allogeneic peripheral blood stem cell and bone marrow transplantation results from a single center: A focus on the incidence of graft-vs.-host disease and relapse

39. A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

40. Mitochondrial serine protease HTRA2 p.G3999S in a kindred with essential tremor and Parkinson disease

45. Identification of a novel missense mutation in RAD51 in a large family with congenital mirror movements

46. Causal mutation discovery using next generation sequencing data: development and application of a pipeline to reduce false positive calls and to map regions of shared homozygosity and IBD

50. Recessive LAMC3 mutations cause malformations of occipital cortical development

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