28 results on '"Soresina, A"'
Search Results
2. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
3. Inborn errors of immunity with atopic phenotypes: A practical guide for allergists
4. Non-contrast MR Lymphography of lipedema of the lower extremities
5. Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality
6. Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome
7. Double-blind, placebo-controlled, randomized trial on low-dose azithromycin prophylaxis in patients with primary antibody deficiencies
8. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
9. Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies
10. Non-contrast Magnetic Resonance Lymphangiography: an emerging technique for the study of lymphedema
11. Chronic Granulomatous Disease in children: a single center experience
12. Ataxia-telangiectasia: Immunodeficiency and survival
13. Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
14. Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease
15. Bruton tyrosine kinase mediates TLR9-dependent human dendritic cell activation
16. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
17. Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity
18. A possible role for B cells in COVID-19? Lesson from patients with agammaglobulinemia
19. Immunophenotype anomalies predict the development of autoimmune cytopenia in 22q11.2 deletion syndrome
20. Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients
21. Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE
22. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome
23. Search for poliovirus long-term excretors among patients affected by agammaglobulinemia
24. Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay
25. Clinical, Immunological, and Molecular Analysis in a Large Cohort of Patients with X-Linked Agammaglobulinemia: An Italian Multicenter Study
26. Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
27. Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease
28. Sa.96. Mutational Analysis of the Pre-BCR Components in 22 Italian Patients with Autosomal Recessive Agammaglobulinemia: Novel Disease Causing Mutations in the mu Heavy Chain Gene and Novel Variants in Both the mu Heavy Chain and λ5 Genes
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