about
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeImmune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO geneIntergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome.Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiencyWiskott-Aldrich syndrome protein-mediated actin dynamics control type-I interferon production in plasmacytoid dendritic cells.Accumulation of peripheral autoreactive B cells in the absence of functional human regulatory T cells.A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.In vivo tracking of T cells in humans unveils decade-long survival and activity of genetically modified T memory stem cells.Longitudinal Evaluation of Immune Reconstitution and B-cell Function After Hematopoietic Cell Transplantation for Primary Immunodeficiency.The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function.Role of reduced intensity conditioning in T-cell and B-cell immune reconstitution after HLA-identical bone marrow transplantation in ADA-SCID.Clinical features and follow-up in patients with 22q11.2 deletion syndrome.Etiology, clinical outcome, and laboratory features in children with neutropenia: analysis of 104 cases.Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia.Delayed early antiretroviral treatment is associated with an HIV-specific long-term cellular response in HIV-1 vertically infected infants.HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders.Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency.Prognostic value of the stromal cell-derived factor 1 3'A mutation in pediatric human immunodeficiency virus type 1 infection.Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients.Combined immunodeficiency due to JAK3 mutation in a child presenting with skin granuloma.Successful simplification of protease inhibitor-based HAART with triple nucleoside regimens in children vertically infected with HIV.Bruton's tyrosine kinase defect in dendritic cells from X-linked agammaglobulinaemia patients does not influence their differentiation, maturation and antigen-presenting cell function.Evaluation of the relevance of humoral immunodeficiencies in a pediatric population affected by recurrent infections.Schimke immunoosseous dysplasia: suggestions of genetic diversity.IgE Immunoadsorption Knocks Down the Risk of Food-Related Anaphylaxis.Evidence of clonotypic pattern of T-cell repertoire in synovial fluid of children with juvenile rheumatoid arthritis at the onset of the disease.A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyConsanguinity and polygenic diseases: a model for antibody deficienciesStructural defects and variations in the HIV-1 nef gene from rapid, slow and non-progressor childrenSwitching from protease inhibitor-based-HAART to a protease inhibitor-sparing regimen is associated with improved specific HIV-immune responses in HIV-infected childrenSerum leptin and CD4+ T lymphocytes in HIV+ children during highly active antiretroviral therapyRestriction in T-Cell Receptor Repertoire in a Patient Affected by Trichothiodystrophy and CD4+LymphopeniaSerratia marcescens Osteomyelitis in a Newborn with Chronic Granulomatous DiseaseEarly-onset monocyte–B–natural killer–dendritic cells’ deficiency successfully treated with hematopoietic stem cell transplantationHumoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)Rapid T-cell Receptor CD4+ Repertoire Reconstitution and Immune Recovery in Unrelated Umbilical Cord Blood Transplanted Pediatric Leukemia PatientsPost-Natal Ontogenesis of the T-Cell Receptor CD4 and CD8 Vβ Repertoire and Immune Function in Children with DiGeorge SyndromeStructural defects and variations in the HIV-1 nef gene from rapid, slow and non-progressor childrenEffect of HLA compatibility, pregnancies, blood transfusions, and taboo mismatches in living unrelated kidney transplantation
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Caterina Cancrini
@ast
Caterina Cancrini
@en
Caterina Cancrini
@es
Caterina Cancrini
@nl
type
label
Caterina Cancrini
@ast
Caterina Cancrini
@en
Caterina Cancrini
@es
Caterina Cancrini
@nl
prefLabel
Caterina Cancrini
@ast
Caterina Cancrini
@en
Caterina Cancrini
@es
Caterina Cancrini
@nl
P106
P1153
6602683164
P1280
P21
P31
P496
0000-0001-8410-9617