Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Francesco Scolari"'
Autor:
Nicola Bossini, Alessandra Pola, Giorgio Depetri, Fabio Battista Viola, Vincenzo Terlizzi, Chiara Salviani, Nicole Zambetti, Francesca Valerio, Chiara Manenti, Michela Tonoli, Stefano Pasquali, Stefano Possenti, Stefania Affatato, Paola Pecchini, Elisa Delbarba, Federico Alberici, Marianna Moscato, Mario Gaggiotti, Fabio Malberti, Francesco Scolari, Camilla Maffei, Laura Econimo
Publikováno v:
American Journal of Transplantation
The outcome of kidney transplant patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is still unclear. Here we describe the clinical characteristics, disease outcome, and risk factors for acute respiratory distress sy
Autor:
Paola Gaggia, Roberta Cortinovis, Francesca Boni, Francesco Scolari, Chiara Saccà, Bernardo Lucca, Roberto Zubani, Alessandra Pola, Elisa Delbarba, Nicola Bossini, Agnese Gallico, Eleonora Calcaterra, Alberto Mucchetti, Stefano Possenti, Federico Alberici, Vincenzo Terlizzi, Mario Gaggiotti, Elena Pezzini, Chiara Manenti, Ester Maria Costantino, Paola Piarulli, Camilla Maffei, Stefania Affatato, Ezio Movilli, Sergio Bove, Laura Econimo, Martina Bracchi, Corrado Camerini, Alice Guerini, Francesca Valerio, Mattia Zappa
Publikováno v:
Kidney International
The SARS-CoV-2 epidemic is pressuring health care systems worldwide. Disease outcomes in certain subgroups of patients are still scarce, and data are needed. Therefore, we describe here the experience of four dialysis centers of the Brescia Renal COV
Autor:
Alessandra Pola, Nicole Zambetti, Margherita Venturini, Stefano Possenti, Francesca Valerio, Nicola Bossini, Francesco Scolari, Chiara Manenti, Stefania Affatato, Camilla Maffei, Federico Alberici, Mario Gaggiotti, Marianna Moscato, Laura Econimo, Elisa Delbarba
Publikováno v:
Kidney International
The outcome of SARS-CoV2 infection in patients who have received a kidney allograft and are being treated with immunosuppression is unclear. We describe 20 kidney transplant recipients (median age 59 years [inter quartile range 51-64 years], median a
Autor:
Susan Moir, Marita Bosticardo, Francesco Castelli, Jeffrey I. Cohen, Danielle Fink, Maria Lorenza Muiesan, Richard Apps, Nicholas Rachmaninoff, Neha Bansal, Jinguo Chen, Eugenia Quiros-Roldan, Helen C. Su, Darius Mostaghimi, Can Liu, John S. Tsang, Michail S. Lionakis, Yu Zhang, Peter D. Burbelo, Kerry Dobbs, Elana Shaw, Matthew P. Mulé, Foo Cheung, Ottavia M. Delmonte, Gabriele Tomasoni, Tae Wook Chun, Camillo Rossi, Michael S. Abers, Luisa Imberti, Pedro Milanez-Almeida, Alessandra Sottini, William W. Lau, Douglas B. Kuhns, Laura Failla, Kyu Lee Han, Luigi D. Notarangelo, Andrew J. Martins, Brian Sellers, Alessandra Tucci, Francesco Scolari, Rachel Sparks
Publikováno v:
Cell
COVID-19 exhibits extensive patient-to-patient heterogeneity. To link immune response variation to disease severity and outcome over time, we longitudinally assessed circulating proteins as well as 188 surface protein markers, transcriptome, and T-ce
Autor:
Chiara Fallerini, Alessandra Renieri, Mirella Bruttini, Simone Furini, Sergio Daga, Anna Maria Pinto, Francesca Mari, Francesco Scolari, Maria Antonietta Mencarelli, Francesca Ariani, Carmine Pecoraro
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-9 (2019)
BMC Nephrology
BMC Nephrology
Background Alport syndrome is a clinically heterogeneous nephropathy characterized by severe symptomatology at kidney level due to ultrastructural lesions of the glomerular basement membrane (GBM) as consequence of mutations in COL4 genes. The diseas
Autor:
Eva Martin, Gianfranco Savoldi, Chiara Dordoni, Claudia Izzi, Laura Econimo, Francesco Scolari, Cinzia Mazza, Elisa Delbarba, Federico Alberici
Causative mutations in the GANAB gene have been described in only 14 families, 9 diagnosed with late-onset Autosomal Dominant Polycystic Kidney Disease (ADPKD) and 5 with Autosomal Dominant Polycystic Liver Disease (ADPLD). Diagnosis of ADPKD was mad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6fa95b3286a253038517d241bb6f6ec
http://hdl.handle.net/11379/546415
http://hdl.handle.net/11379/546415
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:
Simona Fisogni, Andrea Delbarba, Letizia Chiara Pezzaioli, Paolo Facondo, Filippo Maffezzoni, Fabio Facchetti, Carlo Cappelli, Claudia Izzi, Alberto Ferlin, Elena Di Lodovico, Francesco Scolari
Publikováno v:
The Journal of clinical endocrinology and metabolism. 105(12)
Context Apo A-I Leu75Pro is a rare hereditary form of amyloidosis that mainly involves the kidney, the liver, and the testis. Objective To define the characteristics of organ damage and testis impairment in the largest cohort collected to date of men
Autor:
Paola Toniati, Simone Piva, Marco Cattalini, Emirena Garrafa, Francesca Regola, Francesco Castelli, Franco Franceschini, Paolo Airò, Chiara Bazzani, Eva-Andrea Beindorf, Marialma Berlendis, Michela Bezzi, Nicola Bossini, Maurizio Castellano, Sergio Cattaneo, Ilaria Cavazzana, Giovanni-Battista Contessi, Massimo Crippa, Andrea Delbarba, Elena De Peri, Angela Faletti, Matteo Filippini, Micol Frassi, Mario Gaggiotti, Roberto Gorla, Michael Lanspa, Silvia Lorenzotti, Rosa Marino, Roberto Maroldi, Marco Metra, Alberto Matteelli, Denise Modina, Giovanni Moioli, Giovanni Montani, Maria-Lorenza Muiesan, Silvia Odolini, Elena Peli, Silvia Pesenti, Maria-Chiara Pezzoli, Ilenia Pirola, Alessandro Pozzi, Alessandro Proto, Francesco-Antonio Rasulo, Giulia Renisi, Chiara Ricci, Damiano Rizzoni, Giuseppe Romanelli, Mara Rossi, Massimo Salvetti, Francesco Scolari, Liana Signorini, Marco Taglietti, Gabriele Tomasoni, Lina-Rachele Tomasoni, Fabio Turla, Alberto Valsecchi, Davide Zani, Francesco Zuccalà, Fiammetta Zunica, Emanuele Focà, Laura Andreoli, Nicola Latronico
Publikováno v:
Autoimmunity Reviews
A hyperinflammatory syndrome (HIS) may cause a life-threatening acute respiratory distress syndrome (ARDS) in patients with COVID-19 pneumonia. A prospective series of 100 consecutive patients admitted to the Spedali Civili University Hospital in Bre