Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Margherita Chessa"'
Autor:
Jamie Inshaw, Fabio Busonero, Eleonora Porcu, Maristella Pitzalis, Eleonora Cocco, Margherita Chessa, Helen M. Colhoun, Annalisa Loizedda, Marco Masala, Gonçalo R. Abecasis, Maria Giovanna Marrosu, Lidia Leoni, Carlo Sidore, Mario Lovicu, Annapaola Frongia, David Schlessinger, Sandra Lai, Nicolò Curreli, Andrea Maschio, Lenuta Balaci, Liana Ap Ferreli, Fausto Pier'Angelo Poddie, Francesca Virdis, Suna Onengut-Gumuscu, John A. Todd, Michele Marongiu, Valeria Orrù, Maria Rossella Ricciardi, Magdalena Zoledziewska, Antonello Pani, Mariano Dei, Stephen S. Rich, Francesca Deidda, Jessica Frau, Mauro Pala, Nazario Olla, Paola Ferrigno, Edoardo Fiorillo, Gabriella Sole, Alessandro P Delitala, Valentina Serra, Francesco Loi, Stuart J. McGurnaghan, Maristella Steri, Maria Grazia Pilia, Antonella Mulas, Matteo Floris, Francesco Cucca, Luisa Mereu, Catherine C. Robertson
Publikováno v:
Mult Scler
Background: Defective alleles within the PRF1 gene, encoding the pore-forming protein perforin, in combination with environmental factors, cause familial type 2 hemophagocytic lymphohistiocytosis (FHL2), a rare, severe autosomal recessive childhood d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::415d04bc08b8dfe6dc575e1015b48465
https://doi.org/10.1177/1352458520963937
https://doi.org/10.1177/1352458520963937
Autor:
Gavino Pala, Mario Maioli, Margherita Chessa, Stanislao Lostia, Elisabetta Fadda, Gianna Costa, Maria Antonietta Secci, Elisabetta Solla, Valeria Orrù, Cristina Mancosu, Adolfo Pacifico, Rossella Ricciardi, Paola Frongia, Federico Santoni, Maria Antonietta Zedda, Annalisa Nucaro, Lucia Schirru, Stefania Tranquilli, Raffaele Murru, Stefania Cuccu, Daniela Murru, Loredana Moi, Novella Landis, Maria Cristina Melis, Elisabetta Deidda, Daniela Corongiu, Magdalena Zoledziewska, Patrizia Zavattari, Marcella Rolesu, Marcella Devoto, Michael B. Whalen, Anna Franca Milia, M Lai, Maristella Pitzalis, Rosanna Lampis, Anna Maria Marinaro, Costantino Motzo, Maria Giovanna Marrosu, Daniela Contu, Francesco Cucca
Publikováno v:
BMC Med Genet, vol. 9, pp. 3
BMC Medical Genetics
BMC Medical Genetics, Vol 9, Iss 1, p 3 (2008)
BMC Medical Genetics
BMC Medical Genetics, Vol 9, Iss 1, p 3 (2008)
Background The Mediterranean island of Sardinia has a strikingly high incidence of the autoimmune disorders Type 1 Diabetes (T1D) and Multiple Sclerosis (MS). Furthermore, the two diseases tend to be co-inherited in the same individuals and in the sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50a47628e7b89a39191854434f95b34
https://serval.unil.ch/resource/serval:BIB_B731D83E9943.P001/REF.pdf
https://serval.unil.ch/resource/serval:BIB_B731D83E9943.P001/REF.pdf
Autor:
Margherita Chessa, Efisio Angius, Paolo Masile, Rosanna Lampis, Antonio Cao, F Frau, Francesco Cucca, Mario Silvetti, Paola Frongia, Dolores Macis, Mauro Congia, Stefano De Virgiliis
Publikováno v:
Human immunology. 43(4)
The contribution of genetic variation at HLA class II loci to the susceptibility to and protection from IDDM was investigated by analyzing the distribution of HLA-DRB1 ∗ 04 haplotypes in 630 Sardinian newborns and 155 Sardinian IDDM patients. The d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd67f90b402ab3a6e80a5a9487dfd1b0
https://pubmed.ncbi.nlm.nih.gov/7499178
https://pubmed.ncbi.nlm.nih.gov/7499178