about
Type 1 Diabetes in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome (APECED): A "Rare" Manifestation in a "Rare" DiseaseImportin beta: a novel autoantigen in human autoimmunity identified by screening random peptide libraries on phage.Unravelling autoimmune pathogenesis by screening random peptide libraries with human sera.Identification of a common autoantigenic epitope of protein disulfide isomerase, golgin-160 and voltage-gated potassium channel in type 1 diabetes.Altered B cell homeostasis and toll-like receptor 9-driven response in type 1 diabetes carriers of the C1858T PTPN22 allelic variant: implications in the disease pathogenesisExpression of PD-1 Molecule on Regulatory T Lymphocytes in Patients with Insulin-Dependent Diabetes Mellitus.Selection of phage-displayed peptides mimicking type 1 diabetes-specific epitopes.The Impact of Specific Viruses on Clinical Outcome in Children Presenting with Acute Heart Failure.Identification of a novel type 1 diabetes-specific epitope by screening phage libraries with sera from pre-diabetic patients.Role of caspase-8 in thymus function.Endocrine autoimmunity in Turner syndromeUnravelling the role of infectious agents in the pathogenesis of human autoimmunity: the hypothesis of the retroviral involvement revisited.Recents patents for isolating, delivering and tracking adult stem cells in regenerative medicine.Recent insights into the role and molecular mechanisms of the autoimmune regulator (AIRE) gene in autoimmunity.The potential of multimer technologies in type 1 diabetes prediction strategies.Experimental strategies in autoimmunity: antagonists of cytokines and their receptors, nanocarriers, inhibitors of immunoproteasome, leukocyte migration and protein kinases.A pathogenetic approach to autoimmune skin disease therapy: psoriasis and biological drugs, unresolved issues, and future directions.Manipulating thymic apoptosis for future therapy of autoimmune diseases.Identifying thyroid stem/progenitor cells: advances and limitations.The putative role of endoplasmic reticulum aminopeptidases in autoimmunity: insights from genomic-wide association studies.Proteasome inhibitors: a new perspective for treating autoimmune diseases.The putative role of the C1858T polymorphism of protein tyrosine phosphatase PTPN22 gene in autoimmunity.Recent insights on the putative role of autophagy in autoimmune diseases.Recent advances in mesenchymal stem cell immunomodulation: the role of microvesicles.Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of seven additional sicilian patients and overview of the overall series from sicily.Pharmacological modulation of caspase-8 in thymus-related medical conditions.Do mutations of RAG genes have a role in human autoimmunity? The Notarangelo's hypothesis revisited.Gene/environment interactions in the pathogenesis of autoimmunity: new insights on the role of Toll-like receptors.Thyrospheres From Normal or Malignant Thyroid Tissue Have Different Biological, Functional, and Genetic Features.Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells.Isolation and characterization of omental adipose progenitor cells in children: a potential tool to unravel the pathogenesis of metabolic syndrome.Insights into the Diagnostic Potential of Extracellular Vesicles and Their miRNA Signature from Liquid Biopsy as Early Biomarkers of Diabetic Micro/Macrovascular Complications.Family history and ethnicity influencing clinical presentation of type 1 diabetes in childhood.Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.The Continuous Glucose Monitoring System (CGMS) in type 1 diabetic children is the way to reduce hypoglycemic risk.A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).Analysis of the autoimmune regulator gene in patients with autoimmune non-APECED polyendocrinopathies.Central precocious puberty and growth hormone deficiency in a boy with Prader-Willi syndrome.An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).Identification of GAD65 AA 114-122 reactive 'memory-like' NK cells in newly diagnosed Type 1 diabetic patients by HLA-class I pentamers.
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description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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type
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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Alessandra Fierabracci
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P106
P21
P31
P496
0000-0003-3078-9754