檢索結果 - Sandra D’Alfonso

Refine Results
  1. 1
    Mitochondrial DNA sequence variation in multiple sclerosis

    Mitochondrial DNA sequence variation in multiple sclerosis 由 Gregory J. Tranah, Adam Santaniello, Stacy J. Caillier, Sandra D’Alfonso, Filippo Martinelli Boneschi, Stephen L. Hauser, Jorge R. Oksenberg

    出版 2015
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  2. 2
    Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering

    Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering 由 Santosh Anand, Eleonora Mangano, Nadia Barizzone, Roberta Bordoni, Melissa Sorosina, Ferdinando Clarelli, Lucia Corrado, Filippo Martinelli Boneschi, Sandra D’Alfonso, Gianluca De Bellis

    出版 2016
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  3. 3
    HLA alleles modulate EBV viral load in multiple sclerosis

    HLA alleles modulate EBV viral load in multiple sclerosis 由 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

    出版 2018
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  4. 4
    Cytokine gene polymorphism in human disease: on-line databases, Supplement 1

    Cytokine gene polymorphism in human disease: on-line databases, Supplement 1 由 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

    出版 2001
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  5. 5
    Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis

    Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis 由 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

    出版 2012
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    High frequency of<i>TARDBP</i>gene mutations in Italian patients with amyotrophic lateral sclerosis

    High frequency of<i>TARDBP</i>gene mutations in Italian patients with amyotrophic lateral sclerosis 由 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

    出版 2009
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  7. 7
    Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis

    Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 由 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

    出版 2011
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  8. 8
    Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene

    Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene 由 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

    出版 2012
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  9. 9
    Cognitive impairment across ALS clinical stages in a population-based cohort

    Cognitive impairment across ALS clinical stages in a population-based cohort 由 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

    出版 2019
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  10. 10
    Systematic evaluation of genetic mutations in ALS: a population-based study

    Systematic evaluation of genetic mutations in ALS: a population-based study 由 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

    出版 2022
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  11. 11
    HLA-class I markers and multiple sclerosis susceptibility in the Italian population

    HLA-class I markers and multiple sclerosis susceptibility in the Italian population 由 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

    出版 2009
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  12. 12
    Replication of recently identified systemic lupus erythematosus genetic associations: a case–control study

    Replication of recently identified systemic lupus erythematosus genetic associations: a case–control study 由 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

    出版 2009
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus

    Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus 由 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

    出版 2005
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  14. 14
    The multistep hypothesis of ALS revisited

    The multistep hypothesis of ALS revisited 由 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

    出版 2018
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    Immunoproteasome LMP2 60HH Variant Alters MBP Epitope Generation and Reduces the Risk to Develop Multiple Sclerosis in Italian Female Population

    Immunoproteasome LMP2 60HH Variant Alters MBP Epitope Generation and Reduces the Risk to Develop Multiple Sclerosis in Italian Female Population 由 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

    出版 2010
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  16. 16
    STAT4 associates with systemic lupus erythematosus through two independent effects that correlate with gene expression and act additively with IRF5 to increase risk

    STAT4 associates with systemic lupus erythematosus through two independent effects that correlate with gene expression and act additively with IRF5 to increase risk 由 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

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  17. 17
    Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease

    Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease 由 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

    出版 2007
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  18. 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 erythematosus

    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... 由 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

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  19. 19
    Epstein-Barr virus genetic variants are associated with multiple sclerosis

    Epstein-Barr virus genetic variants are associated with multiple sclerosis 由 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

    出版 2015
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  20. 20
    A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

    A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus 由 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

    出版 2008
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: