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1. Technical challenges of intracellular flow cytometry-based assays as a functional complement to diagnosis of signaling defects of inborn errors of immunity: PI3K pathway as a case of study

2. Determining value in the treatment of activated PI3Kδ syndrome in Spain: a multicriteria decision analysis from the perspective of key stakeholders

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3. Predicting anti-TNF treatment response in rheumatoid arthritis: An artificial intelligence-driven model using cytokine profile and routine clinical practice parameters

4. Detection of specific RBD+ IgG+ memory B cells by flow cytometry in healthcare workers and patients with inborn errors of immunity after BNT162b2 m RNA COVID-19 vaccination

5. Familial CD45RA– T cells to treat severe refractory infections in immunocompromised patients

6. Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses

7. Humoral and cellular immune responses to Pfizer-BioNTech BNT162b2 SARS-CoV-2 vaccine in adolescents with liver transplantation: Single center experience

8. Epigenetic profiling linked to multisystem inflammatory syndrome in children (MIS-C): A multicenter, retrospective study

9. Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools

10. Effectiveness of immunosuppression minimisation, conversion or withdrawal strategies in paediatric solid organ and haematopoietic stem cell transplantation: a protocol of a systematic review and meta-analysis

11. A mutation in the promoter region of BTK causes atypical XLA

12. Impaired CpG Demethylation in Common Variable Immunodeficiency Associates With B Cell Phenotype and Proliferation Rate

13. Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond

14. Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

15. Hypomorphic variant in TRNT1 induces a milder autoinflammatory disease with congenital cataracts and impaired sexual development

16. Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed participants (CombiVacS): a multicentre, open-label, randomised, controlled, phase 2 trial

17. COVID-19 and Pembrolizumab-Induced Secondary Hemophagocytic Lymphohistiocytosis: a Case Report

18. Differential effects of the second SARS-CoV-2 mRNA vaccine dose on T cell immunity in naïve and COVID-19 recovered individuals

19. Cytokine Profile in Children with Severe Multisystem Inflammatory Syndrome Related to the Coronavirus Disease 2019

20. Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools

21. Marked changes in innate immunity associated with a mild course of COVID-19 in identical twins with athymia and absent circulating T cells

22. Chilblain-like lesions and COVID-19 infection: A prospective observational study at Spains ground zero

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

24. Colitis expands the phenotype of PAAND patients: new case report and review of the literature

25. A mutation in the promoter region of BTK causes atypical XLA

26. SARS-Cov-2 cysteine-like protease (Mpro) is immunogenic and can be detected in serum and saliva of COVID-19-seropositive individuals

27. Identification of the first cases of complete CD16A deficiency: Association with persistent EBV infection

28. SARS-CoV-2 Cysteine-like Protease Antibodies Can Be Detected in Serum and Saliva of COVID-19–Seropositive Individuals

29. Epigenetic Deregulation in Human Primary Immunodeficiencies

30. Selection and validation of antibody clones against IgG and IgA subclasses in switched memory B-cells and plasma cells

31. Impaired control of multiple viral infections in a family with complete IRF9 deficiency

32. Defects in memory B-cell and plasma cell subsets expressing different immunoglobulin-subclasses in patients with CVID and immunoglobulin subclass deficiencies

33. The EuroFlow PID orientation tube for flow cytometric diagnostic screening of primary immunodeficiencies of the lymphoid system

34. Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases

35. EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System

36. IFITM3 and severe influenza virus infection. No evidence of genetic association

37. Impaired CpG Demethylation in Common Variable Immunodeficiency Associates With B Cell Phenotype and Proliferation Rate

38. The role of respiratory viruses in children with humoral immunodeficiency on immunoglobulin replacement therapy

39. Unexpected High Incidence of Human Herpesvirus-6 Encephalitis after Naive T Cell-Depleted Graft of Haploidentical Stem Cell Transplantation in Pediatric Patients

40. Mutations in XLF/NHEJ1/Cernunnos gene results in downregulation of telomerase genes expression and telomere shortening

41. Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunity

42. Naive T-Cell Depleted Allografts-Graft Engineered Hematopoietic Stem Cell Transplant in Pediatric Patients

43. Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LG

44. Hematopoietic stem cell transplantation for CD3δ deficiency

45. A leaky mutation in CD3D differentially affects αβ and γδ T cells and leads to a Tαβ–Tγδ+B+NK+ human SCID

46. Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

47. NOD2polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

48. New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy

49. Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model

50. A novel mutation in NFKBIA/IKBA results in a degradation-resistant N-truncated protein and is associated with ectodermal dysplasia with immunodeficiency