38 research outputs found

    Analysis of single nucleotide polymorphisms in the FAS and CTLA-4 genes of peripheral T-cell lymphomas

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    Angioimmunoblastic T-cell lymphoma (AILT) represents a subset of T-cell lymphomas but resembles an autoimmune disease in many of its clinical aspects. Despite the phenotype of effector T-cells and high expression of FAS and CTLA-4 receptor molecules, tumor cells fail to undergo apoptosis. We investigated single nucleotide polymorphisms (SNPs) of the FAS and CTLA-4 genes in 94 peripheral T-cell lymphomas. Although allelic frequencies of some FAS SNPs were enriched in AILT cases, none of these occurred at a different frequency compared to healthy individuals. Therefore, SNPs in these genes are not associated with the apoptotic defect and autoimmune phenomena in AILT

    Penicillamine-related neurological syndrome in a child affected by Wilson disease with hepatic presentation

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    Treatment of pediatric hepatitis C: results and perspectives

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    Side effects of ALPHA-interferon therapy and impact on health-related quality of life in children with chronic viral hepatitis

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    Lack of intrafamilial transmission of hepatitits C virus in family memebers of children with chronic hepatitis C infection

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    Is alpha-interferon usefull in children with nonB, non C chronic hepatitis ?

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    Lymphoblastoid alpha-interferon therapy in chronic hepatitis-C

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    Cryptogenic chronic hepatitis in childwood is unrelated to hepatitis G virus

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    Fas/Apo1 mutations and autoimmune lymphoproliferative syndrome in a patient with type two autoimmene hepatitis

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