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

2. COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report

3. Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease

5. ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling

6. A critical view on autoantibodies in lupus nephritis: Concrete knowledge based on evidence

11. Discovery of a Peptide Nucleic Acid (PNA) aptamer for cardiac troponin I: Substituting DNA with neutral PNA maintains picomolar affinity and improves performances for electronic sensing with graphene field-effect transistors (gFET)

12. Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches

15. Deficiency in coatomer complex I causes aberrant activation of STING signalling

16. Analysis of pulmonary features and treatment approaches in the COPA syndrome.

18. HSP90β controls NLRP3 autoactivation

19. Effect of anakinra on mortality in patients with COVID-19: a systematic review and patient-level meta-analysis

20. EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay

21. Interleukin-1 blockade in patients with Wiskott-Aldrich syndrome: a retrospective multinational case series

22. Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients

24. The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children

25. Therapeutic Role of HPV Vaccination on Benign HPV-induced Epithelial Proliferations in Immunocompetent and Immunocompromised Patients: Case Study and Review of the Literature.

26. Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality

27. Vasculitis and vasculopathy associated with inborn errors of immunity: an overview

29. Inborn error of WAS presenting with SARS-CoV-2-related multisystem inflammatory syndrome in children

30. Novel heterozygous TREX1 mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a case report

31. Lupus Nephritis Patterns and Response to Type I Interferon in Patients With DNASE1L3Variants: Report of Three Cases

32. Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome

33. The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan–Deficient Muscular Dystrophy

36. Proposta di un algoritmo diagnostico per il deficit di Adenosina Deaminasi-2 (DADA2).

37. Supramolecular Nucleic Acid-Based Organosilica Nanoparticles Responsive to Physical and Biological Inputs

38. Responsive Nucleic Acid-Based Organosilica Nanoparticles

40. T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency

41. Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome

43. Blood Lymphocyte Subsets and Proinflammatory Cytokine Profile in ROHHAD(NET) and non-ROHHAD(NET) Obese Individuals

44. Case Report: Multisystem inflammatory syndrome in children with associated proximal tubular injury

45. Expert Perspective: Diagnostic Approach to the Autoinflammatory Diseases.

46. Hyperactivated PI3Kδ promotes self and commensal reactivity at the expense of optimal humoral immunity

47. ARF1 prevents aberrant type I IFN induction by regulating STING activation and recycling

49. Hematopoietic stem cell transplantation for inborn errors of immunity: 30-year single-center experience

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