نتائج البحث - Sandra D’Alfonso
- يعرض 1 - 20 نتائج من 51
- اذهب إلى الاصفحة التالية
-
1
-
2
Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering حسب Santosh Anand, Eleonora Mangano, Nadia Barizzone, Roberta Bordoni, Melissa Sorosina, Ferdinando Clarelli, Lucia Corrado, Filippo Martinelli Boneschi, Sandra D’Alfonso, Gianluca De Bellis
منشور في 2016Artigo -
3
HLA alleles modulate EBV viral load in multiple sclerosis حسب Simone Agostini, Roberta Mancuso, Franca Rosa Guerini, Sandra D’Alfonso, Cristina Agliardi, Ambra Hernis, Milena Zanzottera, Nadia Barizzone, Maurizio Leone, Domenico Caputo, Marco Rovaris, Mario Clerici
منشور في 2018Artigo -
4
Cytokine gene polymorphism in human disease: on-line databases, Supplement 1 حسب Jeff L. Bidwell, Leigh Keen, Grant Gallagher, Robert P. Kimberly, T. Huizinga, Michael McDermott, Jorge R. Oksenberg, J McNicholl, Flemming Pociot, Cornelia Hardt, Sandra D’Alfonso
منشور في 2001Revisão -
5
Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis حسب Donato Gemmati, G Zeri, Elisa Orioli, Francesca E De Gaetano, Fabrizio Salvi, Ilaria Bartolomei, Sandra D’Alfonso, C. Dall’Osso, Maurizio Leone, Ajay Singh, Rosanna Asselta, Paolo Zamboni
منشور في 2012Artigo -
6
High frequency of<i>TARDBP</i>gene mutations in Italian patients with amyotrophic lateral sclerosis حسب Lucia Corrado, Antonia Ratti, Cinzia Gellera, Emanuele Buratti, Barbara Castellotti, Yari Carlomagno, Nicola Ticozzi, Letizia Mazzini, Lucia Testa, Franco Taroni, Francisco E. Baralle, Vincenzo Silani, Sandra D’Alfonso
منشور في 2009Artigo -
7
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis حسب Roberto Del Bo, Cinzia Tiloca, Viviana Pensato, Lucia Corrado, Antonia Ratti, Nicola Ticozzi, Stefania Corti, Barbara Castellotti, Letizia Mazzini, Gianni Sorarù, Cristina Cereda, Sandra D’Alfonso, Cinzia Gellera, Giacomo P. Comi, Vincenzo Silani
منشور في 2011Artigo -
8
Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene حسب Sara Emelie Löfgren, Johan Frostegård, Lennart Truedsson, Bernardo A. Pons‐Estel, Sandra D’Alfonso, T Witte, Bernard Lauwerys, E. Endreffy, László Kovács, Carlos Vasconcelos, Berta Martins da Silva, Sergey V. Kozyrev, Marta E. Alarcón‐Riquelme
منشور في 2012Artigo -
9
Cognitive impairment across ALS clinical stages in a population-based cohort حسب Adriano Chió, Cristina Moglia, Antonio Canosa, Umberto Manera, Rosario Vasta, Maura Brunetti, Marco Barberis, Lucia Corrado, Sandra D’Alfonso, Enrica Bersano, Maria Francesca Sarnelli, Valentina Solara, Jean Pierre Zucchetti, Laura Peotta, Barbara Iazzolino, Letizia Mazzini, Gabriele Mora, Andrea Calvo
منشور في 2019Artigo -
10
Systematic evaluation of genetic mutations in ALS: a population-based study حسب Maurizio Grassano, Andrea Calvo, Cristina Moglia, Luca Sbaiz, Maura Brunetti, Marco Barberis, Federico Casale, Umberto Manera, Rosario Vasta, Antonio Canosa, Sandra D’Alfonso, Lucia Corrado, Letizia Mazzini, Clifton L. Dalgard, Ramita Karra, Ruth Chia, Bryan J. Traynor, Adriano Chió
منشور في 2022Artigo -
11
HLA-class I markers and multiple sclerosis susceptibility in the Italian population حسب Laura Bergamaschi, Maurizio Leone, M. Fasano, Franca Rosa Guerini, Daniela Ferrante, Elisabetta Bolognesi, N Barizzone, Lucia Corrado, Paola Naldi, Cristina Agliardi, Ennia Dametto, Marco Salvetti, Andrea Visconti, Daniela Galimberti, Elio Scarpini, Marco Vercellino, Roberto Bergamaschi, Francesco Monaco, Domenico Caputo, Patricia Momigliano‐Richiardi, Sandra D’Alfonso
منشور في 2009Artigo -
12
Replication of recently identified systemic lupus erythematosus genetic associations: a case–control study حسب Marian Suarez-Gestal, Manuel Calaza, Emöke Endreffy, R Pullmann, Josep Ordi‐Ros, Gian Domenico Sebastiani, Š Rùzicková, María José Santos, Chryssa Papasteriades, Maurizio Marchini, Fotini N. Skopouli, Ana Suárez, Francisco J. Blanco, Sandra D’Alfonso, Marc Bijl, Patrícia Carreira, Torsten Witte, S. Migliaresi, Juan J. Gómez‐Reino, Antonio González
منشور في 2009Artigo -
13
Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus حسب Sandra D’Alfonso, Nadia Barizzone, Mara Giordano, Annalisa Chiocchetti, Corrado Magnani, Luca Castelli, Manuela Indelicato, Francesca Giacopelli, Maurizio Marchini, R Scorza, Maria Giovanna Danieli, M. Cappelli, S. Migliaresi, B. Bigliardo, M G Sabbadini, Elena Baldissera, M. Galeazzi, Gian Domenico Sebastiani, Giovanni Minisola, Roberto Ravazzolo, Umberto Dianzani, Patricia Momigliano‐Richiardi
منشور في 2005Artigo -
14
The multistep hypothesis of ALS revisited حسب Adriano Chió, Letizia Mazzini, Sandra D’Alfonso, Lucia Corrado, Antonio Canosa, Cristina Moglia, Umberto Manera, Enrica Bersano, Maura Brunetti, Marco Barberis, Jan H. Veldink, Leonard H. van den Berg, Neil Pearce, William Sproviero, Russell L. McLaughlin, Alice Vajda, Orla Hardiman, James Rooney, Gabriele Mora, Andrea Calvo, Ammar Al‐Chalabi
منشور في 2018Artigo -
15
Immunoproteasome LMP2 60HH Variant Alters MBP Epitope Generation and Reduces the Risk to Develop Multiple Sclerosis in Italian Female Population حسب Michele Mishto, Elena Bellavista, Claudia Ligorio, Kathrin Textoris‐Taube, Aurelia Santoro, Mara Giordano, Sandra D’Alfonso, Florinda Listı̀, Benedetta Nacmias, Elena Cellini, Maurizio Leone, Luigi Maria Grimaldi, Chiara Fenoglio, Federica Esposito, Filippo Martinelli Boneschi, Daniela Galimberti, Elio Scarpini, Ulrike Seifert, Maria Pia Amato, Calogero Caruso, Maria Pia Foschini, Peter M. Kloetzel, Claudio Franceschi
منشور في 2010Artigo -
16
STAT4 associates with systemic lupus erythematosus through two independent effects that correlate with gene expression and act additively with IRF5 to increase risk حسب Anna-Karin Abelson, A M Delgado-Vega, Sergey V. Kozyrev, Elena Sánchez, Rafael Velázquez‐Cruz, Niclas Eriksson, Jérôme Wojcik, Mitsu Reddy, Guadalupe Lima, Sandra D’Alfonso, S. Migliaresi, Vicente Baca, Lorena Orozco, T Witte, Norberto Ortego‐Centeno, Hadi Abderrahim, Bernardo A. Pons‐Estel, Carlos Gutiérrez, Ana Suárez, María Francisca González‐Escribano, Javier Martı́n, Marta E. Alarcón‐Riquelme
منشور في 2008Artigo -
17
Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease حسب Mauro D’Amato, Sara Bruce, Francesca Bresso, Marco Zucchelli, Sini Ezer, Ville Pulkkinen, Cecilia M. Lindgren, Marco Astegiano, Mario Rizzetto, Paolo Gionchetti, Gabriele Riegler, R. Sostegni, Marco Daperno, Sandra D’Alfonso, Patricia Momigliano‐Richiardi, Leif Törkvist, Pauli Puolakkainen, Maarit Lappalainen, Paulina Paavola–Sakki, Leena Halme, Martti Färkkilâ, Ulla Turunen, Kimmo Kontula, Robert Löfberg, Sven Pettersson, Juha Kere
منشور في 2007Artigo -
18
A 3′‐untranslated region variant is associated with impaired expression of <i>CD226</i> in T and natural killer T cells and is associated with susceptibility to systemic lupus eryt... حسب Sara Emelie Löfgren, A M Delgado-Vega, Caroline J. Gallant, Elena Sánchez, Johan Frostegård, Lennart Truedsson, Enrique de Ramón Garrido, José Mario Sabio, María F. González‐Escribano, Bernardo A. Pons‐Estel, Sandra D’Alfonso, Torsten Witte, Bernard Lauwerys, Emöke Endreffy, László Kovács, Carlos Vasconcelos, Berta Martins da Silva, Javier Martı́n, Marta E. Alarcón‐Riquelme, Sergey V. Kozyrev
منشور في 2010Artigo -
19
Epstein-Barr virus genetic variants are associated with multiple sclerosis حسب Rosella Mechelli, Caterina Manzari, Claudia Policano, Anita Annese, Ernesto Picardi, Renato Umeton, Arianna Fornasiero, Anna Maria D’Erchia, Maria Chiara Buscarinu, Cristina Agliardi, Viviana Annibali, Barbara Serafini, Barbara Rosicarelli, Silvia Romano, Daniela F. Angelini, Vito A. G. Ricigliano, Fabio Buttari, Luca Battistini, Diego Centonze, Franca Rosa Guerini, Sandra D’Alfonso, Graziano Pesole, Marco Salvetti, Giovanni Ristori
منشور في 2015Artigo -
20
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus حسب Valeria Orrù, Si‐Yu Tsai, Blanca Rueda‐Medina, Edoardo Fiorillo, Stephanie M. Stanford, J. Dasgupta, Jaana Hartiala, Леи Жао, Norberto Ortego‐Centeno, Sandra D’Alfonso, F C Arnett, Hui Wu, Miguel Á. González‐Gay, Betty P. Tsao, Bernardo A. Pons‐Estel, Marta E. Alarcón‐Riquelme, Yantao He, Z.-Y. Zhang, Hooman Allayee, Xiaojiang S. Chen, Javier Martı́n, Nunzio Bottini
منشور في 2008Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Medicine
Gene
Immunology
Disease
Internal medicine
Genotype
Amyotrophic lateral sclerosis
Single-nucleotide polymorphism
Multiple sclerosis
Allele
Genome-wide association study
Population
Environmental health
Genetic association
Antibody
Computational biology
Neuroscience
Pathology
Mutation
Antigen
Computer science
Immune system
Locus (genetics)
Odds ratio
C9orf72
Dementia
Frontotemporal dementia
Human leukocyte antigen