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

2. Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet)

3. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia.

4. Antibody Deficiency in Patients with Biallelic KARS1 Mutations

6. Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job’s syndrome

7. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

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

9. Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations

10. The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)

11. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis

12. Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network

13. MicroRNA dysregulation in ataxia telangiectasia.

14. Clinical Manifestations of 22q11.2 Deletion Syndrome

15. Case report: EBV-related eye orbits and sinuses lymphohistiocytic infiltration responsive to rituximab in a patient with X lymphoproliferative syndrome type 1

17. DiGeorge Syndrome

21. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

22. A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency.

26. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors

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

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

31. Rare solid tumors in a patient with Wiskott–Aldrich syndrome after hematopoietic stem cell transplantation: case report and review of literature

34. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

37. Expandig Lentiviral Vectors cargo capacity with protein trans-splicing

38. Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease

39. Clinical and immunological phenotypes of selective IgM deficiency in children: Results from a multicenter study.

41. Targeted treatment of autoimmune cytopenias in primary immunodeficiencies

42. Long term longitudinal follow up of AD-HIES cohort: impact of early diagnosis and enrolment to IPINet centres on natural history of Job's Syndrome

43. Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency

45. Epigenetic Alterations in Inborn Errors of Immunity

46. Activated phosphoinositide 3‐dinase delta syndrome (APDS): An update

48. Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity

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