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pro vyhledávání: '"S. de Virgiliis"'
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Autor:
Giangennaro Coppola, A. Pascotto, Loredana Boccone, E Ciccimarra, S De Virgiliis, Pietro Vajro
Publikováno v:
Neuropediatrics. 33:180-185
We describe 3 children (2 siblings aged 10 and 3 years, and 1 sporadic case aged 13 years) with cerebellar vermis defect associated with oligophrenia, congenital ataxia, and hepatic fibrocirrhosis. Differently from what is reported in COACH syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e71e21f30caca93a7bf20c8aa16ef03
https://doi.org/10.1055/s-2002-34492
https://doi.org/10.1055/s-2002-34492
Publikováno v:
Tissue Antigens. 58:402-406
Celiac disease (CD) is a multifactorial disorder of the small intestine caused by a permanent dietary intolerance to gluten. The combined presence of the HLA class II DQA1 * 0501 and DQB1 * 0201 alleles represents the majorgenetic component for disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::199b6f3e9cddc8aca3f15400d0bec979
https://doi.org/10.1034/j.1399-0039.2001.580609.x
https://doi.org/10.1034/j.1399-0039.2001.580609.x
Autor:
S. De Virgiliis, Rosanna Lampis, Laura Cornelia Clotilde Morelli, Mauro Congia, Francesco Cucca
Publikováno v:
Tissue Antigens. 56:515-521
In this study we have established the frequencies of the DRB1-DQA1-DQB1 haplotypes in a large cohort of Sardinian new-borns and found that the most frequent haplotypes were detected at frequencies unique to the Sardinians. Other haplotypes, common in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63305af9301bd0f99d8f49a1b08a63f6
https://doi.org/10.1034/j.1399-0039.2000.560605.x
https://doi.org/10.1034/j.1399-0039.2000.560605.x
Autor:
Maria Grazia Clemente, F Frau, M P Musu, S. De Virgiliis, Gino Roberto Corazza, Gabriella Sole, G. Brusco
Publikováno v:
Gut. 47:520-526
BACKGROUND—The cytoskeleton actin network of intestinal microvilli has been found to be rapidly impaired after gluten challenge in coeliac disease (CD). The aim of this study was to investigate the presence of an immune reaction towards cytoskeleto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd4e86e8d1cce7c7234b8f95ac3b257c
https://doi.org/10.1136/gut.47.4.520
https://doi.org/10.1136/gut.47.4.520
Autor:
F Frau, Maria Grazia Clemente, Me Lai, Mauro Congia, A.P. Mazzoleni, C Dessi, Antonio Cao, Rosanna Lampis, S. De Virgiliis, Francesco Cucca
Publikováno v:
Hepatology. 24:1338-1341
To investigate the factors that may confer susceptibility or protection to hepatitis C virus (HCV) infection and to HCV-associated immunological disorders, we designed two studies on 420 Sardinian transfusion-dependent thalassemia patients followed i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ba4c62687e86f8d95df374817d2556
https://doi.org/10.1002/hep.510240603
https://doi.org/10.1002/hep.510240603
Autor:
G. Faa, Antonio Cao, G. Cornacchia, Franco Lilliu, Maria Grazia Clemente, Mauro Congia, A.P. Mazzoleni, G. Diana, A. Melis, S. De Virgiliis, F Frau, M.R. Frau, C Dessi, Rosanna Lampis, Me Lai
Publikováno v:
The Journal of Pediatrics. 125:123-128
The purpose of this study was to determine whether interferon-alfa (IFN-alpha) therapy benefits patients with transfusion-dependent thalassemia and chronic active hepatitis C, and whether their iron burden modifies the response to this therapy. We co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4eeaf30fe962a50858f82463ea79c3b
https://doi.org/10.1016/s0022-3476(94)70138-5
https://doi.org/10.1016/s0022-3476(94)70138-5
Autor:
Enrico Schirru, M. Scarpa, Rita-Désirée Jores, Mauro Congia, Rossano Rossino, F. Oppia, P. Usai-Satta, M. Doloretta Macis, Francesco Cucca, S. De Virgiliis, V. Corona, F. Loriga
Publikováno v:
European journal of clinical nutrition. 61(10)
Objective: Recently, the C/T-13910 polymorphism on chromosome 2q21 in North-European populations has been found completely associated with lactase activity and its genetic typing proposed as first-stage screening test for adult hypolactasia. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d401a01a2fbbfddd84820fdaed69eba
https://pubmed.ncbi.nlm.nih.gov/17311063
https://pubmed.ncbi.nlm.nih.gov/17311063
Autor:
P Strisciuglio, Lucia Cicotto, M P Musu, Mauro Congia, Mg Clemente, Gino Roberto Corazza, Tarcisio Not, Umberto Volta, G. Gasbarrini, S. De Virgiliis, Gabriella Sole, Giuseppe Maggiore, Carolina Ciacci, Riccardo Troncone, Alessio Fasano, Elena Neri
This study describes a new method to detect autoantibodies against actin filaments (AAA) as a serological marker of intestinal villous atrophy (IVA) in celiac disease (CD), and reports the results of an Italian double-blind multicenter study.IgA-AAA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d2f8a417a18ff23be378fab6663df00
http://hdl.handle.net/11568/87171
http://hdl.handle.net/11568/87171
Autor:
M P Musu, J S Kang, Mauro Congia, S. De Virgiliis, M R Di Pierro, Maria Grazia Clemente, Alessio Fasano, R Macatagney, Sandro Drago
Background and aims: Despite the progress made in understanding the immunological aspects of the pathogenesis of coeliac disease (CD), the early steps that allow gliadin to cross the intestinal barrier are still largely unknown. The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02265e891a7cc36a7a23d8b312e16521
https://europepmc.org/articles/PMC1774976/
https://europepmc.org/articles/PMC1774976/