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2. Increased bronchiolitis burden and severity after the pandemic: a national multicentric study

4. A Nationwide Study of GATA2 Deficiency in Italy Reveals Novel Symptoms and Genotype–phenotype Association

7. Impact of COVID-19 infection on lung function and nutritional status amongst individuals with cystic fibrosis: A global cohort study

8. A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome

10. 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

11. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

12. Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo

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

16. Non tutti gli ascessi sono infetti

17. Clinical course and risk factors for severe COVID-19 among Italian patients with cystic fibrosis: a study within the Italian Cystic Fibrosis Society

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

19. SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response

21. Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations

23. Off-label use of combined antiretroviral therapy, analysis of data collected by the Italian Register for HIV-1 infection in paediatrics in a large cohort of children

24. MicroRNA dysregulation in ataxia telangiectasia.

25. Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for the Treatment of Participants With WHIM Syndrome: Investigational Assessment of Lymphocyte Subpopulations in Peripheral Blood

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

27. A COUNTRYWIDE STUDY OF GATA2 DEFICIENCY IN ITALY REVEALS NOVEL SYMPTOMS AND GENOTYPE-PHENOTYPE CORRELATION

28. Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation

30. The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)

31. Impact of a diagnostic therapeutic educational pathway program for asthma management in preschool children

32. Genetic Variants Assessing Crohn’s Disease Pattern in Pediatric Inflammatory Bowel Disease Patients by a Clinical Exome Survey

33. Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

35. Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies

37. Early anakinra treatment improves cardiac outcome of multisystem inflammatory syndrome in children, regardless of disease severity.

38. Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function

43. Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study

45. Longitudinal Characterization of Immune Response in a Cohort of Children Hospitalized with Multisystem Inflammatory Syndrome

46. European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance

49. COVID-19 Pneumonia with Migratory Pattern in Agammaglobulinemic Patients: A Report of Two Cases and Review of Literature

50. CARD11 dominant negative mutation leads to altered human Natural Killer cell homeostasis

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