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1. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

2. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

3. Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

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

6. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

10. Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature

11. Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis

12. Neurodevelopmental outcome of preterm very low birth weight infants admitted to an Italian tertiary center over an 11-year period

15. Exposure to Gastric Acid Inhibitors Increases the Risk of Infection in Preterm Very Low Birth Weight Infants but Concomitant Administration of Lactoferrin Counteracts This Effect

16. Host genomics of the HIV-1 reservoir size and its decay rate during suppressive antiretroviral treatment

17. Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts

18. COVID‐19 associated severe mucocutaneous blistering eruptions: A case series

19. Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients

20. Fulminant echovirus 11 hepatitis in male non-identical twins in northern Italy, April 2023

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

23. Determinants of HIV-1 reservoir size and long-term dynamics during suppressive ART

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

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

28. La visibilità della Chiesa. Schmitt e Agostino.

29. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

30. Genomic alterations in human umbilical cord–derived mesenchymal stromal cells call for stringent quality control before any possible therapeutic approach

31. In vitro affinity for nicotine of soft contact lenses of different materials

32. How to: Diagnose inborn errors of intrinsic and innate immunity to viral, bacterial, mycobacterial, and fungal infections

36. Isolated congenital asplenia: An overlooked cause of thrombocytosis

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

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

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

41. Autoantibodies Against Type I IFNs in Patients with Ph-Negative Myeloproliferative Neoplasms

42. Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature

46. A Pilot Study on Covid and Autism: Prevalence, Clinical Presentation and Vaccine Side Effects

47. Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature

48. Immunological lessons from genome-wide association studies of infections

49. Autoantibodies neutralizing type I IFNs underlie severe tick-borne encephalitis in ∼10% of patients

50. Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study

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