394 results on '"Soresina, Annarosa"'
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2. Impaired arterial dilation and increased NOX2 generated oxidative stress in subjects with ataxia-telangiectasia mutated (ATM) kinase
3. 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
4. In adult X-CGD patients, regulatory T cells are expanded while activated T cells display a NOX2-independent ROS increase
5. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
6. Immune tolerance breakdown in inborn errors of immunity: Paving the way to novel therapeutic approaches
7. The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)
8. Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network
9. MicroRNA dysregulation in ataxia telangiectasia.
10. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
11. Inborn errors of immunity with atopic phenotypes: A practical guide for allergists
12. Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality
13. Vasculitis and vasculopathy associated with inborn errors of immunity: an overview
14. The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)
15. Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet)
16. Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
17. Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies
18. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
19. Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies
20. Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function
21. Chronic Granulomatous Disease in children: a single center experience
22. Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study
23. Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
24. Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature
25. Ataxia-telangiectasia: Immunodeficiency and survival
26. Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
27. COVID-19 Pneumonia with Migratory Pattern in Agammaglobulinemic Patients: A Report of Two Cases and Review of Literature
28. Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
29. Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease
30. In vivo effects of dexamethasone on blood gene expression in ataxia telangiectasia
31. Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography
32. Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation
33. Neurovisual Assessment in Children with Ataxia Telangiectasia
34. Impaired platelet activation in patients with hereditary deficiency of p47phox
35. 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
36. Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency
37. Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Immunodeficiency in Routine Clinical Practice: The VISPO Prospective Multicenter Study
38. Pathogenesis of Autoimmune Cytopenias in Inborn Errors of Immunity Revealing Novel Therapeutic Targets
39. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
40. When a Nontuberculous Mycobacterial Infection Reveals an Error of Immunity
41. Activated phosphoinositide 3‐dinase delta syndrome (APDS): An update
42. Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings
43. Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study
44. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
45. Molecular characterization of a large cohort of patients with Chronic Granulomatous Disease and identification of novel CYBB mutations: An Italian multicenter study
46. Thymic Epithelial Cell Alterations and Defective Thymopoiesis Lead to Central and Peripheral Tolerance Perturbation in MHCII Deficiency
47. Efficacy and Safety of Subcutaneous Vivaglobin® Replacement Therapy in Previously Untreated Patients with Primary Immunodeficiency: A Prospective, Multicenter Study
48. Effectiveness of Immunoglobulin Replacement Therapy on Clinical Outcome in Patients with Primary Antibody Deficiencies: Results from a Multicenter Prospective Cohort Study
49. A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia
50. The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia
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