about
Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variantHLA-DQB1*0201 homozygosis predisposes to severe intestinal damage in celiac diseaseHLA class II transgenic mice: models of the human CD4+ T-cell immune response.The distribution of HLA class II haplotypes reveals that the Sardinian population is genetically differentiated from the other Caucasian populations.DRB1*0401-restricted human T cell clone specific for the major proinsulin73-90 epitope expresses a down-regulatory T helper 2 phenotype.Early effects of gliadin on enterocyte intracellular signalling involved in intestinal barrier function.T cell epitopes of insulin defined in HLA-DR4 transgenic mice are derived from preproinsulin and proinsulin.Identification of immunodominant T cell epitopes of human glutamic acid decarboxylase 65 by using HLA-DR(alpha1*0101,beta1*0401) transgenic mice.Genetic variants regulating immune cell levels in health and disease.T cell responses to a human cartilage autoantigen in the context of rheumatoid arthritis-associated and nonassociated HLA-DR4 alleles.Anti-actin IgA antibodies identify celiac disease patients with a Marsh 3 intestinal damage among subjects with moderate anti-TG2 levels.Prudence is necessary in the application of the new ESPGHAN criteria for celiac disease omitting duodenal biopsy: a case report.Frequency of the thiopurine S-methyltransferase alleles in the ancient genetic population isolate of Sardinia.High meat consumption is associated with type 1 diabetes mellitus in a Sardinian case-control study.HLA class II genes in chronic hepatitis C virus-infection and associated immunological disorders.Prevalence of autoimmune thyroiditis in children with celiac disease and effect of gluten withdrawal.Lactose malabsorption: Genetic testing versus lactose hydrogen breath test.Serum lipoproteins and cancer.Genetic testing is ready to change the diagnostic scenario of lactose malabsorption.Decline of lactase activity and c/t-13910 variant in Sardinian childhood.Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia.HLA-DQB1*0305 and -DQB1*0304 alleles among Sardinians. Evolutionary and practical implications for oligotyping.Identification of a novel T-insertion polymorphism at the DMD locus.A novel HLA-DQB1 allele: evidence for gene conversion event promoted by chi-like sequence at DQB1 locus.Autoimmune polyendocrine syndrome type 1: an extensive longitudinal study in Sardinian patients.The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases.Enterocyte Actin Autoantibody Detection: A New Diagnostic Tool in Celiac Disease Diagnosis: Results of a Multicenter StudyGenotyping of the Lactase-Phlorizin Hydrolase C/T-13910Polymorphism by Means of a New Rapid Denaturing High-Performance Liquid Chromatography-Based Assay in Healthy Subjects and Colorectal Cancer PatientsHeterogeneity in the Magnitude of the Insulin Gene Effect on HLA Risk in Type 1 DiabetesRole of Predisposing and Protective HLA-DQA and HLA-DQB Alleles in Sardinian Multiple SclerosisDetermination of glutamic acid decarboxylase 65 peptides presented by the type I diabetes-associated HLA-DQ8 class II molecule identifies an immunogenic peptide motifA high frequency of the A30, B18, DR3, DRw52, DQw2 extended haplotype in Sardinian celiac disease patients: further evidence that disease susceptibility is conferred by DQ A1*0501, B1*0201The HLA DQB1*0502 allele is neutrally associated with insulin-dependent diabetes mellitus in the Sardinian populationDeferoxamine-induced growth retardation in patients with thalassemia majorDifferent HLA DR2-DQw1 haplotypes in Sardinian and northern Italian populations: implications for multiple sclerosis susceptibilityYeast-derived hepatitis B vaccine in thalassaemic patients: a preliminary reportCryoglobulinemia in transfusion-dependent thalassemia majorThe distribution of DR4 haplotypes in Sardinia suggests a primary association of type I diabetes with DRB1 and DQB1 lociEffect of iron overload on the response to recombinant interferon-alfa treatment in transfusion-dependent patients with thalassemia major and chronic hepatitis C
P50
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P50
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հետազոտող
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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Mauro Congia
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P106
P21
P31
P496
0000-0003-1688-304X