Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Isabella Pisani"'
Autor:
Giovanni Maria Rossi, Caterina Mele, Lucio Manenti, Federico Ricco, Francesco Fontana, Isabella Pisani, Enrico Fiaccadori, Renzo Mignani, Micaela Gentile, Elena Bresin, Francesco Paolo Pilato, Marco Delsante
Publikováno v:
Journal of Nephrology. 35:1091-1100
IgA nephropathy (IgAN) has been anecdotally reported in association with atypical hemolytic uremic syndrome (aHUS). The association likely portends poor renal outcome, and the possible relationship with complement overactivation has yet to be elucida
Autor:
Damiano Marastoni, Stefano Ziccardi, Marco Pitteri, Massimiliano Calabrese, Richard Nicholas, Francesco Pezzini, Anna Isabella Pisani, Roberta Magliozzi
Publikováno v:
Multiple Sclerosis Journal. 28:768-777
Background: The cerebrospinal fluid (CSF) molecular milieu is a marker of diffuse intrathecal inflammation in the meninges that, in turn, targets the grey matter (GM) in multiple sclerosis (MS). Cognitive impairment (CI) is associated with brain dama
Autor:
Maurizio Bruschi, Andrea Angeletti, Xhuliana Kajana, Gabriella Moroni, Renato Alberto Sinico, Micaela Fredi, Augusto Vaglio, Lorenzo Cavagna, Federico Pratesi, Paola Migliorini, Francesco Locatelli, Giulia Pazzola, Giampaola Pesce, Marcello Bagnasco, Angelo Manfredi, Giuseppe Alvise Ramirez, Pasquale Esposito, Simone Negrini, Federica Bui, Barbara Trezzi, Giacomo Emmi, Ilaria Cavazzana, Valentina Binda, Paride Fenaroli, Isabella Pisani, Carlomaurizio Montecucco, Domenico Santoro, Francesco Scolari, Stefano Volpi, Marta Mosca, Angela Tincani, Giovanni Candiano, Enrico Verrina, Franco Franceschini, Angelo Ravelli, Marco Prunotto, Pier Luigi Meroni, Gian Marco Ghiggeri
Publikováno v:
Journal of autoimmunity. 132
Mechanisms for the generation of anti-dsDNA autoantibodies are still not completely elucidated. One theory states that dsDNA interacts for mimicry with antibodies raised versus other antigens but molecular features for mimicry are unknown. Here we sh
Autor:
Antonio Scalfari, Chiara Romualdi, Anna Isabella Pisani, Francesco Crescenzo, Massimiliano Calabrese
Publikováno v:
European Journal of Neurology
Background At patient-level, the prognostic value of several features that are known to be associated with an increased risk of converting from relapsing remitting (RR) to secondary phase (SP) multiple sclerosis (MS), remain limited. Methods Among 26
Autor:
Verena Klämbt, Youying Mao, Vimla Aggarwal, Arang Kim, Friedhelm Hildebrandt, Mohamad A. Mikati, Vandana Shashi, Anne H. O’Donnell-Luria, Vaidehi Jobanputra, Jeremiah Martino, Vivette D. D'Agati, Minxian Wang, Marcus R. Benz, Shoji Yano, Janine Altmüller, Ali G. Gharavi, Florian Buerger, Enrico Fiaccadori, Richard P. Lifton, Bodo B. Beck, Amy Kolb, Mordi Muorah, David Goldstein, Nina Mann, Martin R. Pollak, Dina Ahram, Heidi Cope, Gian Marco Ghiggeri, Jillian S. Parboosingh, Asmaa S. AbuMaziad, Kamal Khan, Ana C. Onuchic-Whitford, Louise Bier, Emma Pierce-Hoffman, Jonathan E. Zuckerman, Shrikant Mane, Moin A. Saleem, Amar J. Majmundar, Heidi L. Rehm, Ora Yadin, Erin L. Heinzen, Gina Y. Jin, Christelle Moufawad El Achkar, Konstantin Deutsch, Julia Hoefele, Ania Koziell, Gianluca Caridi, Talha Gunduz, Agnieszka Bierzynska, Korbinian M. Riedhammer, Monica Bodria, Ronen Schneider, Julian A. Martinez-Agosto, Thomas M. Kitzler, Shirlee Shril, Ulrike John-Kroegel, Howard Trachtman, Adele Mitrotti, Eleanor G. Seaby, Amanda V. Tyndall, Isabella Pisani, Patricia L. Weng, Tze Y Lim, A. Micheil Innes, John Musgrove, Simone Sanna-Cherchi, Erica E. Davis
Publikováno v:
Am J Hum Genet
Focal segmental glomerulosclerosis (FSGS) is the main pathology underlying steroid-resistant nephrotic syndrome (SRNS) and a leading cause of chronic kidney disease. Monogenic forms of pediatric SRNS are predominantly caused by recessive mutations, w
Autor:
Massimiliano Calabrese, Francesco Crescenzo, Francesca B. Pizzini, Albulena Bajrami, Roberta Magliozzi, Damiano Marastoni, Anna Isabella Pisani
Background: The underlying pathogenesis of surface-in grey matter abnormalities in MS, demonstrated by both neuropathology and advanced MRI analyses, is under investigation and it might be related to CSF-mediated mechanism of inflammation and/or dama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71319ba000dbebd4e234691da259a36f
http://hdl.handle.net/11562/1047394
http://hdl.handle.net/11562/1047394
Autor:
Stefania Rossi, M. Calabrese, Damiano Marastoni, Stefania Montemezzi, Francesca Benedetta Pizzini, Anna Isabella Pisani, Francesco Crescenzo, Anna Bolzan, Roberta Magliozzi
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
article-version (Version of Record) 3
Background and ObjectivesTo evaluate the extent of intrathecal inflammation in patients with primary progressive MS (PPMS) at the time of diagnosis and to define markers and a specific inflammatory profile capable of distinguishing progressive from r
Autor:
Simone Negrini, Paola Migliorini, Angelo Ravelli, Marcello Bagnasco, Marta Mosca, Andrea Angeletti, Giampaola Pesce, Carlomaurizio Montecucco, Augusto Vaglio, Gabriella Moroni, Francesco Locatelli, Paride Fenaroli, Giacomo Emmi, Barbara Trezzi, Ilaria Cavazzana, Isabella Pisani, Giuseppe A. Ramirez, Valentina Binda, Maurizio Bruschi, Angela Tincani, Lorenzo Cavagna, Renato Alberto Sinico, Enrico Verrina, Francesco Scolari, Stefano Volpi, Leda Cipriani, Franco Franceschini, Gian Marco Ghiggeri, Pasquale Esposito, Giuseppe Murdaca, Federico Pratesi, Giovanni Candiano, Micaela Fredi, Andrea Petretto, Marco Prunotto, Giacomo Garibotto, Angelo A. Manfredi, Giulia Pazzola, Domenico Santoro
Publikováno v:
Rheumatology (Oxford)
Objectives Serum anti-dsDNA and anti-nucleosome IgGs have been proposed as signatures for SLE and LN in limited numbers of patients. We sought to show higher sensitivity and specificity of the same antibodies with the IgG2 isotype and included IgG2 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e1ca75f4df99f5f7b36df1270b3575
http://hdl.handle.net/10281/298460
http://hdl.handle.net/10281/298460
Autor:
Paride Fenaroli, Enrico Verrina, Paola Migliorini, Renato Alberto Sinico, Leda Cipriani, Angelo A. Manfredi, Francesco Locatelli, Marta Mosca, Federico Pratesi, Angelo Ravelli, Marcello Bagnasco, Augusto Vaglio, Giulia Pazzola, Micaela Fredi, Andrea Petretto, Carlomaurizio Montecucco, Barbara Trezzi, Franco Franceschini, Valentina Binda, Domenico Santoro, Giacomo Garibotto, Giovanni Candiano, Marco Prunotto, Francesco Scolari, Giuseppe A. Ramirez, Giacomo Emmi, Matteo D'Alessandro, Isabella Pisani, Andrea Angeletti, Giampaola Pesce, Simone Negrini, Pasquale Esposito, Giuseppe Murdaca, Angela Tincani, Gabriella Moroni, Gian Marco Ghiggeri, Ilaria Cavazzana, Stefano Volpi, Maurizio Bruschi, Lorenzo Cavagna
Publikováno v:
Rheumatology (Oxford, England)
Objectives Circulating anti-ENO1 and anti-H2A IgG2 have been identified as specific signatures of LN in a cross-over approach. We sought to show whether the same antibodies identify selected population of patients with LN with potentially different c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0018ed11196c9336a992bad38951b00
http://hdl.handle.net/10281/297796
http://hdl.handle.net/10281/297796
Autor:
Taner Basturk, Ali G. Gharavi, Patrick Hamilton, Nan Chen, Kai-Uwe Eckardt, Weiming Wang, Paul Brenchley, Olivia Balderes, Dong Ki Kim, Elisabet Ars, Antonio Amoroso, Mehmet Sukru Sever, Neil Ashman, Bartosz Foroncewicz, Dan Zhang, Maddalena Marasa, Francesca Lugani, Elion Hoxha, Mario Bonomini, Gang Liu, Detlef Bockenhauer, Hakki Arikan, Pietro A. Canetta, Bruno Vogt, Magdalena Durlik, Carlo Sidore, Abdulmecit Yildiz, Mehmet Koc, Magdalena Zoledziewska, Simone Sanna-Cherchi, Antonello Pani, Domenico Santoro, Francesca Zanoni, Landino Allegri, Matthias Kretzler, Ireneusz Habura, Claudia Izzi, Naomi Issler, Carmelita Marcantoni, Isabella Pisani, Monica Bodria, Hajeong Lee, Krzysztof Mucha, Ruth J. F. Loos, Lawrence H. Beck, Laura H. Mariani, Rolf A.K. Stahl, Eimear E. Kenny, Gonca E. Karahan, Pierre Ronco, Robert Kleta, Francesco Scolari, José Ballarín, Francesco Londrino, Bénédicte Stengel, Dario Roccatello, Atlas Khan, Belong Cho, Gerald B. Appel, Lili Liu, Xiaofan Hu, Savas Ozturk, Karla Mehl, Ming hui Zhao, Ruth J. Pepper, Shreeram Akilesh, Zhao Cui, Yifu Li, Anna Köttgen, Lambertus A. Kiemeney, Fatih Ozay, Jack F.M. Wetzels, Stephen H. Powis, Jun Zhang, Silvana Savoldi, Hong Ren, Matthias Wuttke, John O. Connolly, Yon Su Kim, Gianluigi Zaza, Chris Cheshire, Simona Granata, Andrew S. Bomback, Nurhan Seyahi, Donatella Spotti, Vladimir Tesar, Stephanie Dufek, Fernando C. Fervenza, Krzysztof Kiryluk, Barbara Moszczuk, Leszek Pączek, Agnieszka Perkowska-Ptasińska, Nikol Mladkova, Shelly Harris, Loreto Gesualdo, Hitoshi Suzuki, Jin Ho Park, Jana Reiterova, Julia M. Hofstra, Francesco Cucca, Li Lin, Laila Yasmin Mani, Sanjana Gupta, Ben Sprangers, Iuliana Ionita-Laza, Daniel C. Cattran, Gian Marco Ghiggeri, Sebahat Akgul, Horia Stanescu, Matthew G. Sampson, Piergiorgio Messa, Xialian Yu, Marieke J H Coenen, Hanna Debiec, Jingyuan Xie, Jing Xu, Yasar Caliskan, Raphael J. Rosen, Priya Krithivasan, Marco Galliani
Publikováno v:
Nature Communications
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Xie, Jingyuan; Liu, Lili; Mladkova, Nikol; Li, Yifu; Ren, Hong; Wang, Weiming; Cui, Zhao; Lin, Li; Hu, Xiaofan; Yu, Xialian; Xu, Jing; Liu, Gang; Caliskan, Yasar; Sidore, Carlo; Balderes, Olivia; Rosen, Raphael; Bodria, Monica; Zanoni, Francesca; Zhang, Yun; Krithivasan, Priya; ... (2020). The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Nature communications, 11(1), p. 1600. Nature Publishing Group 10.1038/s41467-020-15383-w
r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
Nature Communications, 11
Nature Communications, 11, 1
Xie, J, Liu, L, Mladkova, N, Li, Y, Ren, H, Wang, W, Cui, Z, Hu, X, Yu, X, Liu, G, Caliskan, Y, Sidore, C, Balderes, O, Rosen, R J, Bodria, M, Zanoni, F, Krithivasan, P, Mehl, K, Marasa, M, Khan, A, Ozay, F, Canetta, P A, Bomback, A S, Appel, G B, Sanna-Cherchi, S, Sampson, M G, Mariani, L H, Perkowska-Ptasinska, A, Durlik, M, Mucha, K, Moszczuk, B, Foroncewicz, B, Pączek, L, Habura, I, Ars, E, Ballarin, J, Mani, L-Y, Vogt, B, Ozturk, S, Yildiz, A, Seyahi, N, Arikan, H, Koc, M, Basturk, T, Karahan, G, Akgul, S U, Sever, M S, Zhang, D, Hamilton, P, Kleta, R & Brenchley, P 2020, ' The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis ', Nature Communications, vol. 11, no. 1, pp. 1600 . https://doi.org/10.1038/s41467-020-15383-w
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Xie, Jingyuan; Liu, Lili; Mladkova, Nikol; Li, Yifu; Ren, Hong; Wang, Weiming; Cui, Zhao; Lin, Li; Hu, Xiaofan; Yu, Xialian; Xu, Jing; Liu, Gang; Caliskan, Yasar; Sidore, Carlo; Balderes, Olivia; Rosen, Raphael; Bodria, Monica; Zanoni, Francesca; Zhang, Yun; Krithivasan, Priya; ... (2020). The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Nature communications, 11(1), p. 1600. Nature Publishing Group 10.1038/s41467-020-15383-w
r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
Nature Communications, 11
Nature Communications, 11, 1
Xie, J, Liu, L, Mladkova, N, Li, Y, Ren, H, Wang, W, Cui, Z, Hu, X, Yu, X, Liu, G, Caliskan, Y, Sidore, C, Balderes, O, Rosen, R J, Bodria, M, Zanoni, F, Krithivasan, P, Mehl, K, Marasa, M, Khan, A, Ozay, F, Canetta, P A, Bomback, A S, Appel, G B, Sanna-Cherchi, S, Sampson, M G, Mariani, L H, Perkowska-Ptasinska, A, Durlik, M, Mucha, K, Moszczuk, B, Foroncewicz, B, Pączek, L, Habura, I, Ars, E, Ballarin, J, Mani, L-Y, Vogt, B, Ozturk, S, Yildiz, A, Seyahi, N, Arikan, H, Koc, M, Basturk, T, Karahan, G, Akgul, S U, Sever, M S, Zhang, D, Hamilton, P, Kleta, R & Brenchley, P 2020, ' The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis ', Nature Communications, vol. 11, no. 1, pp. 1600 . https://doi.org/10.1038/s41467-020-15383-w
Vogt, Bruno/0000-0002-1548-6387; Dufek, Stephanie/0000-0002-6323-6673; Liu, Lili/0000-0002-2622-9669; Paczek, Leszek/0000-0003-0160-3009; Cui, Zhao/0000-0002-5837-1926; amoroso, antonio/0000-0002-9437-9407; Rosen, Raphael/0000-0003-1025-1965; Loos, R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2891f6f81e786be552d26cf13e755862
https://hdl.handle.net/11424/243224
https://hdl.handle.net/11424/243224