200 results on '"Brigida, Immacolata"'
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2. Antimicrobial Synergistic Effects of Linezolid and Vancomycin with a Small Synthesized 2-Mercaptobenzothiazole Derivative: A Challenge for MRSA Solving
3. Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study
4. Effect of Methyl-β-Cyclodextrin on the antimicrobial activity of a new series of poorly water-soluble benzothiazoles
5. B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients
6. T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
7. Antimicrobial Synergistic Effects of Linezolid and Vancomycin with a Small Synthesized 2-Mercaptobenzothiazole Derivative: A Challenge for MRSA Solving
8. The case of an APDS patient: Defects in maturation and function and decreased in vitro anti-mycobacterial activity in the myeloid compartment
9. Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency
10. Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child With Intermittent Neutropenia
11. B-cell reconstitution after lentiviral vector–mediated gene therapy in patients with Wiskott-Aldrich syndrome
12. Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection
13. Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency
14. Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity
15. T-cell suicide gene therapy prompts thymic renewal in adults after hematopoietic stem cell transplantation
16. HIV-1 envelope-dependent restriction of CXCR4-using viruses in child but not adult untransformed CD4+ T-lymphocyte lines
17. Alterations in the adenosine metabolism and CD39/CD73 adenosinergic machinery cause loss of Treg cell function and autoimmunity in ADA-deficient SCID
18. Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency
19. In vivo T-cell dynamics during immune reconstitution after hematopoietic stem cell gene therapy in adenosine deaminase severe combined immune deficiency
20. Lentiviral-Mediated Gene Therapy for the Treatment of Adenosine Deaminase 2 Deficiency
21. Defective B cell tolerance in adenosine deaminase deficiency is corrected by gene therapy
22. Integration profile of retroviral vector in gene therapy treated patients is cell‐specific according to gene expression and chromatin conformation of target cell
23. Hematopoietic stem cell gene therapy for adenosine deaminase deficient-SCID
24. Gene therapy for immunodeficiency due to adenosine deaminase deficiency
25. Follicular helper T cell signature of replicative exhaustion, apoptosis and senescence in common variable immunodeficiency
26. C1-3 Immune reconstitution after gene therapy for adenosine deaminase severe combined immunodeficiency (ADA-SCID)
27. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency
28. Effect of Methyl-β-Cyclodextrin on the antimicrobial activity of a new series of poorly water-soluble benzothiazoles
29. A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency
30. Purine metabolism, immune reconstitution, and abdominal adipose tumor after gene therapy for adenosine deaminase deficiency
31. A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
32. FRI0540 A NOVEL AUTOINFLAMMATORY DISEASE CHARACTERIZED BY NEONATAL-ONSET CYTOPENIA WITH AUTOINFLAMMATION, RASH, AND HEMOPHAGOCYTOSIS (NOCARH) DUE TO ABERRANT CDC42 FUNCTION
33. Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
34. Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
35. First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia
36. ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation
37. Apixaban: Effective and Safe in Preventing Thromboembolic Events in Patients with Atrial Fibrillation and Renal Failure
38. A novel genomic inversion in Wiskott-Aldrich–associated autoinflammation
39. First Occurrence of Plasmablastic Lymphoma in Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Disease Patient and Review of the Literature
40. Biological Evaluation of Hyperforin and Its Hydrogenated Analogue on Bacterial Growth and Biofilm Production
41. Apixaban: Effective and Safe in Preventing Thromboembolic Events in Patients with Atrial Fibrillation and Renal Failure
42. Biological and functional characterization of bone marrow-derived mesenchymal stromal cells from patients affected by primary immunodeficiency
43. Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection
44. ACTIVATING N-RAS SOMATIC MUTATION CAUSES AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME
45. NEXT GENERATION SEQUENCING FOR THE IDENTIFICATION OF MAGT1 DELETIONAL EVENT ASSOCIATED WITH KAPOSI SARCOMA
46. Altered B cell development and fuctions in Adenosine Deaminase deficient patients
47. Next-Generation Sequencing Reveals A JAGN1Mutation in a Syndromic Child With Intermittent Neutropenia
48. In vitro synergy testing of anidulafungin with fluconazole, tioconazole, 5-flucytosine and amphotericin B against some Candida spp
49. T-cell defects in patients with ARPC1Bgermline mutations account for combined immunodeficiency
50. Biological Evaluation of Hyperforin and Its Hydrogenated Analogue on Bacterial Growth and Biofilm Production
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