Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Lampasona, V."'
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Protein tyrosine phosphatase-like IA-2 is a major autoantigen in insulin-dependent diabetes. It has been identified as both a specificity of cytoplasmic islet cell Abs and one of the precursors of the 40- and 37-kDa tryptic fragment islet autoantigen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebfdf3c77b6cc9948f77a62c113a8f9e
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030587162&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0030587162&partnerID=MN8TOARS
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
The majority of patients with insulin-dependent diabetes (IDDM) have Abs to 40- and/or 37-kDa tryptic fragments (37/40K-Abs) deriving from an unidentified islet cell membrane protein distinct from glutamate decarboxylase (GAD). Recently, autoantibodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cec61c0dd21d5e182040ec6c5f7d1031
http://europepmc.org/abstract/med/7594559
http://europepmc.org/abstract/med/7594559
Autor:
Pier Alberto Testoni, Rosalia Curto, Federica Barzaghi, Olaf Neth, Maria Grazia Roncarolo, Alessandro Aiuti, Francesca Tucci, Claudia Sartirana, Laura Passerini, Rosa Bacchetta, Vito Lampasona, Graziano Barera, Daniele Zama, Maria Pia Cicalese, Elena Bazzigaluppi, Manfred Hoenig, Ansgar Schulz, Alberto Mariani, Sven Olek, Luca Albarello, Ivana Rabbone, Emanuele Bosi, Markus G. Seidel
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Background] Immune-dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is a lethal disease caused by mutations in a transcription factor critical for the function of thymus-derived regulatory T (Treg) cells (ie, FOXP3), resultin
Mild SARS-CoV-2 Infection After Gene Therapy in a Child With Wiskott-Aldrich Syndrome: A Case Report
Autor:
Sabina Cenciarelli, Valeria Calbi, Federica Barzaghi, Maria Ester Bernardo, Chiara Oltolini, Maddalena Migliavacca, Vera Gallo, Francesca Tucci, Federico Fraschetta, Elena Albertazzi, Elena Sophia Fratini, Giulia Consiglieri, Stefania Giannelli, Francesca Dionisio, Claudia Sartirana, Sara Racca, Chiara Camesasca, Giovanni Peretto, Rita Daverio, Antonio Esposito, Francesco De Cobelli, Paolo Silvani, Marco Rabusin, Andrea Cara, Daria Trabattoni, Stefania Dispinseri, Gabriella Scarlatti, Lorenzo Piemonti, Vito Lampasona, Maria Pia Cicalese, Alessandro Aiuti, Francesca Ferrua
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology, Vol 11 (2020)
In this work we present the case of SARS-CoV-2 infection in a 1.5-year-old boy affected by severe Wiskott-Aldrich Syndrome with previous history of autoinflammatory disease, occurring 5 months after treatment with gene therapy. Before SARS-CoV-2 infe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::872f4a244681d5b6fb19e7f9251d53d5
Autor:
Howard W. Davidson, Ilaria Marzinotto, Cristina Brigatti, Ludovica Dottori, Gianluca Esposito, Elena Bazzigaluppi, Edith Lahner, Vito Lampasona, F. Baldaro, Lorenzo Piemonti, Emanuele Dilaghi
Publikováno v:
Journal of Translational Autoimmunity, Vol 4, Iss, Pp 100131-(2021)
Journal of Translational Autoimmunity
Journal of Translational Autoimmunity
Background Corpus atrophic gastritis (CAG) may lead to intrinsic factor (IF) deficiency and vitamin B12 malabsorption. Intrinsic factor autoantibodies (IFA) are considered markers of pernicious anemia, but their clinical utility in CAG has not been e
Autor:
Marina Ferrarini, Riccardo Biavasco, Lorenzo Dagna, Andreas von Deimling, Maria Giulia Cangi, Claudio Doglioni, Alvise Berti, B. Guglielmi, Maria Grazia Sabbadini, Corrado Campochiaro, Vito Lampasona, Greta Grassini, Giulio Cavalli, Elena DalCin
Objectives Erdheim-Chester disease (ECD) is a rare form of histiocytosis characterised by uncontrolled chronic inflammation. The oncogenic BRAF V600E mutation has been reported in biopsies in 19 out of 37 patients with ECD from the largest published
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8943ab4336313ba9aa8fcc0b890b90b8
Autor:
Vito Lampasona, Gian Franco Bottazzo, Bruno Giometto, Cristina Belloni, Ezio Bonifacio, Marika Vianello, Emanuele Bosi, Sandra Piquer, Elena Bazzigaluppi
Publikováno v:
Clinical immunology (Orlando, Fla.). 117(1)
Glutamic acid decarboxylase (GAD) is an autoantigen in stiff man syndrome (SMS) and type 1 diabetes (TIDM). Different GAD autoantibody characteristics in these disorders have suggested distinct underlying mechanisms of autoimmunity. Here, it is shown
Autor:
Anna Venerando, Elena Bazzigaluppi, Ezio Bonifacio, Graziano Barera, Emanuele Bosi, Cesare Bianchi, Giuseppe Chiumello, Vito Lampasona
Tissue transglutaminase C has recently been identified as one of the auto-antigens of endomysial antibodies found in coeliac disease. In this study we have cloned the human autoantigen and developed immunoassays measuring antibodies to transglutamina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9316f934fc4cac9f09b542ac2d9da875
Considerable evidence exists that the genes coding for the HLA class II DQ molecules in the MHC region are major contributors to genetic susceptibility in insulin-dependent diabetes. Located centromeric to the DQ loci are the genes encoding DMA and D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e7bc9a40e53e666b3ab2270517f8344