Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lucia Schirru"'
Autor:
Patrizia Natali, Roberta Bedin, Gaetano Bernardi, Elena Corsini, Eleonora Cocco, Lucia Schirru, Ilaria Crespi, Marta Lamonaca, Arianna Sala, Cinzia Nicolò, Massimiliano Di Filippo, Alfredo Villa, Viviana Nociti, Teresa De Michele, Paola Cavalla, Paola Caropreso, Francesca Vitetta, Maria Rosaria Cucinelli, Matteo Gastaldi, Tommaso Trenti, Patrizia Sola, Diana Ferraro, on behalf of RIREMS (Rising Researchers in MS)
Publikováno v:
Biomolecules, Vol 12, Iss 5, p 677 (2022)
The kappa index (K-Index), calculated by dividing the cerebrospinal fluid (CSF)/serum kappa free light chain (KFLC) ratio by the CSF/serum albumin ratio, is gaining increasing interest as a marker of intrathecal immunoglobulin synthesis. However, dat
Externí odkaz:
https://doaj.org/article/843d1afdc24640c0b4bd21e92817eb33
Autor:
Eleonora Cocco, Alessandra Meloni, Maria Rita Murru, Daniela Corongiu, Stefania Tranquilli, Elisabetta Fadda, Raffaele Murru, Lucia Schirru, Maria Antonietta Secci, Gianna Costa, Isadora Asunis, Stefania Cuccu, Giuseppe Fenu, Lorena Lorefice, Nicola Carboni, Gioia Mura, Maria Cristina Rosatelli, Maria Giovanna Marrosu
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41678 (2012)
Vitamin D response elements (VDREs) have been found in the promoter region of the MS-associated allele HLA-DRB1*15:01, suggesting that with low vitamin D availability VDREs are incapable of inducing *15:01 expression allowing in early life autoreacti
Externí odkaz:
https://doaj.org/article/681972ee6990452aa896122b232f7594
Autor:
Patrizia Sola, Roberta Bedin, Giancarlo Coghe, Claudia Sardu, Maria Giovanna Marrosu, Diana Ferraro, Lucia Schirru, Jessica Frau, Giuseppe Fenu, Maria Antonietta Secci, Lorena Lorefice, Eleonora Cocco, Luisa M. Villar
Oligoclonal IgM (OCMB) and IgG (OCGB) bands were found to be associated with poor multiple sclerosis (MS) prognosis. We aimed to evaluate the prognostic value of OCMB/OCGB in a cohort of Sardinian MS patients. We recruited patients from the Universit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec122385b053b19d43c18c0d5d8c5118
https://hdl.handle.net/11380/1150408
https://hdl.handle.net/11380/1150408
Autor:
Lorena Lorefice, Jessica Frau, Lucia Schirru, Gianna Costa, Maria Antonietta Secci, Claudia Sardu, Maria Giovanna Marrosu, Giuseppe Fenu, Giancarlo Coghe, M.A. Barracciu, Vincenzo Sechi, Eleonora Cocco
Publikováno v:
Multiple sclerosis (Houndmills, Basingstoke, England). 25(1)
Background: The strongest genetic determinant for multiple sclerosis (MS) is located at the human leukocyte antigen (HLA) class II DRB1 and DQB1 loci. Objectives: To investigate the possible role of predisposing HLA genotypes in determining brain atr
Autor:
Lorena Lorefice, Eleonora Cocco, M.A. Barracciu, Giuseppe Fenu, Jessica Frau, F. Contu, M. Arru, Francesco Cabras, L. Loi, Vincenzo Sechi, V. Melas, Gianna Costa, Maria Antonietta Secci, Mg Marrosu, Giancarlo Coghe, Lucia Schirru, Cristina Melis
Publikováno v:
Multiple sclerosis and related disorders. 19
Background Oligoclonal bands of IgG (OB) are proposed as an early prognostic factor of the disease. Growing attention is directed towards brain volume evaluation as a possible marker of the severity of MS. Previous studies found that MS patients lack
Autor:
Lucia Schirru, Elisabetta Fadda, Giuseppe Fenu, Stefania Cuccu, Eleonora Cocco, Daniela Corongiu, Alessandra Meloni, Maria Rita Murru, Maria Giovanna Marrosu, Maria Cristina Rosatelli, Gianna Costa, Maria Antonietta Secci, Isadora Asunis, Raffaele Murru, Gioia Mura, Lorena Lorefice, Nicola Carboni, Stefania Tranquilli
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41678 (2012)
PLoS ONE
PLoS ONE
Vitamin D response elements (VDREs) have been found in the promoter region of the MS-associated allele HLA-DRB1*15:01, suggesting that with low vitamin D availability VDREs are incapable of inducing *15:01 expression allowing in early life autoreacti
Environment and sustainability are key issues for the policy maker. A policy should be first designed and realistically inserted in its proper context (regional, national, European) in order to be correctly assessed. After that, suitable models need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e40f2f3f1da5221ae0222ff48320c15
http://crenos.unica.it/crenos/node/3401
http://crenos.unica.it/crenos/node/3401
Publikováno v:
Contributions to Statistics ISBN: 9783790821390
In this paper, we disagree on the opportunity to use the double deflation method to produce an equilibrating system of account at a constant price. In fact, by relaxing such a condition, by means of the single deflation method, we obtain a measure of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b48e0aa10890f1a1227870892ebe68f7
https://doi.org/10.1007/978-3-7908-2140-6_10
https://doi.org/10.1007/978-3-7908-2140-6_10
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:
Lucia Schirru, Mg Mascia, Gabriella Spinicci, Eleonora Cocco, Gianluca Floris, Mg Marrosu, Marco Mura, Gianna Costa, Maria Valeria Cherchi
Publikováno v:
Neurology. 66(1)
The authors describe four members of a family with a novel P284S presenilin 1 mutation presenting a clinical phenotype characterized by early-onset dementia, paratetraparesis, dysarthria, dysphagia, and marked involvement of brain white matter. The d