Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Francesco Scolari"'
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:
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
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
Autor:
Paola Migliorini, Paolo Cravedi, Maricla Galetti, Angela Tincani, Francesco Scolari, Giacomo Garibotto, Laura Santucci, Andrea Petretto, Giovanni Candiano, Giulia Pazzola, Micaela Fredi, Giacomo Emmi, Simone Negrini, Gabriella Moroni, Giuseppe A. Ramirez, Renato Alberto Sinico, Franco Franceschini, Silvana Belletti, Paola Ramoino, Paolo Bianchini, Landino Allegri, Alice Bonanni, Gian Marco Ghiggeri, Augusto Vaglio, Marcello Bagnasco, Roberta Bertelli, Francesca Pupo, Angelo Ravelli, Maurizio Bruschi, Federico Pratesi, Lorenzo Cavagna, Angelo A. Manfredi, Domenico Santoro, Stefano Volpi, Federico Mattana, Francesco Puppo, Giampaola Pesce
Publikováno v:
J Rheumatol
Objective.Neutrophil extracellular traps (NET) expose modified antigens for autoantibodies in vasculitis. Little is known about levels and removal pathways of NET in systemic lupus erythematosus (SLE), especially in lupus nephritis (LN). We determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2188d3f8dbf9f1fc60769952c02578c
http://hdl.handle.net/11570/3181511
http://hdl.handle.net/11570/3181511
Autor:
David Fasel, Magdalena Janezcko, Miguel Verbitsky, Katarina Vukojević, Monica Bodria, Edgar A. Otto, Hila Milo Rasouly, Virginia Vega-Warner, Marijan Saraga, Jeremiah Martino, Landino Allegri, Iuliana Ionita-Laza, Adele Mitrotti, Krzysztof Kiryluk, Joanna A.E. van Wijk, Richard P. Lifton, Claudia Izzi, David Goldstein, Vinicio Goj, Loreto Gesualdo, Velibor Tasic, Shrikant Mane, Ali G. Gharavi, Matthew G. Sampson, Adela Arapović, Gianluigi Ardissino, Young Ji Na, Marcin Zaniew, Rik Westland, Francesco Scolari, Simone Sanna-Cherchi, Erica E. Davis, Christopher E. Gillies, Shirlee Shril, Friedhelm Hildebrandt, Lorraine Fievet, Anna Materna-Kiryluk, Anna Latos-Bielenska, Cathy Mendelsohn, Valentina P Capone, Gabriel Makar, Qingxue Liu, Priya Krithivasan, Kamal Khan, Sitharthan Kamalakaran, Nicholas Katsanis, Gian Marco Ghiggeri, Igor Pediaditakis, Maddalena Gigante
Publikováno v:
Sanna-Cherchi, S, Khan, K, Westland, R, Krithivasan, P, Fievet, L, Rasouly, H M, Ionita-Laza, I, Capone, V P, Fasel, D A, Kiryluk, K, Kamalakaran, S, Bodria, M, Otto, E A, Sampson, M G, Gillies, C E, Vega-Warner, V, Vukojevic, K, Pediaditakis, I, Makar, G S, Mitrotti, A, Verbitsky, M, Martino, J, Liu, Q, Na, Y J, Goj, V, Ardissino, G, Gigante, M, Gesualdo, L, Janezcko, M, Zaniew, M, Mendelsohn, C L, Shril, S, Hildebrandt, F, van Wijk, J A E, Arapovic, A, Saraga, M, Allegri, L, Izzi, C, Scolari, F, Tasic, V, Ghiggeri, G M, Latos-Bielenska, A, Kiryluk, A M, Mane, S, Goldstein, D B, Lifton, R P, Katsanis, N, Davis, E E & Gharavi, A G 2017, ' Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations ', American journal of human genetics, vol. 101, no. 5, pp. 789-802 . https://doi.org/10.1016/j.ajhg.2017.09.018
American journal of human genetics, 101(5), 789-802. Cell Press
American journal of human genetics, 101(5), 789-802. Cell Press
Renal agenesis and hypodysplasia (RHD) are major causes of pediatric chronic kidney disease and are highly genetically heterogeneous. We conducted whole-exome sequencing in 202 case subjects with RHD and identified diagnostic mutations in genes known
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c3a42ca76a4b241c69576911f5ac925
https://research.vumc.nl/en/publications/7a1c3557-be57-428b-a383-e7214d46b178
https://research.vumc.nl/en/publications/7a1c3557-be57-428b-a383-e7214d46b178
Autor:
Hana Flögelová, Marijan Saraga, Maria Szczepańska, John M Darlow, Nicholas Katsanis, Barry Honig, Donald Petrey, Ali Samii, Akira Imamoto, Adele Mitrotti, Vladimir J Lozanovski, Bradley A. Warady, Max Werth, Qingxue Liu, Susan L. Furth, Mirna Saraga-Babić, Silvia E. Racedo, Grażyna Krzemień, Yangfan P. Liu, Rik Westland, Christopher E. Gillies, Iain A. Drummond, Alba Carrea, Matthew G. Sampson, Nicholas J Steers, Rémi Salomon, Rong Deng, Valentina P Capone, V. D’Agati, Virginia E. Papaioannou, Richard P. Lifton, Katarina Vukojević, Claudia Izzi, Małgorzata Mizerska-Wasiak, Francesco Scolari, Marcin Tkaczyk, Joanna A.E. van Wijk, Gabriel Makar, Prem Puri, Esther Lopez-Rivera, Loreto Gesualdo, Bernice E. Morrow, Jonathan Barasch, Velibor Tasic, Marcin Zaniew, Cécile Jeanpierre, Adela Arapović, Asaf Vivante, Donna M. McDonald-McGinn, Terrence B. Crowley, Monica Bodria, Daniele Cusi, Wassila Carpentier, Craig S. Wong, Ali G. Gharavi, Miguel Verbitsky, David Fasel, Zhonghai Yan, Edgar A. Otto, David E. Barton, Zoran Gucev, Monika Miklaszewska, Virginia Vega-Warner, Dorota Drozdz, Jeremiah Martino, Elaine H. Zackai, Agnieszka Szmigielska, Anna Latos-Bielenska, Mariarosa Maiorana, Anna Materna-Kiryluk, Landino Allegri, Dominique Gaillard, Laurence Heidet, Friedhelm Hildebrandt, Hakon Hakonarson, Gian Marco Ghiggeri, Simone Sanna-Cherchi, Nenad Kunac, Przemysław Sikora, Emilio Casolari, Krzysztof Kiryluk, Blair R. Anderson
Publikováno v:
New England Journal of Medicine, 376(8), 742-754. Massachussetts Medical Society
Lopez-Rivera, E, Liu, Y P, Verbitsky, M, Anderson, B R, Capone, V P, Otto, E A, Yan, Z, Mitrotti, A, Martino, J, Steers, N J, Fasel, D A, Vukojevic, K, Deng, R, Racedo, S E, Liu, Q, Werth, M, Westland, R, Vivante, A, Makar, G S, Bodria, M, Sampson, M G, Gillies, C E, Vega-Warner, V, Maiorana, M, Petrey, D S, Honig, B, Lozanovski, V J, Salomon, R, Heidet, L, Carpentier, W, Gaillard, D, Carrea, A, Gesualdo, L, Cusi, D, Izzi, C, Scolari, F, Van Wijk, J A E, Arapovic, A, Saraga-Babic, M, Saraga, M, Kunac, N, Samii, A, McDonald-McGinn, D M, Crowley, T B, Zackai, E H, Drozdz, D, Miklaszewska, M, Tkaczyk, M, Sikora, P, Szczepanska, M, Mizerska-Wasiak, M, Krzemien, G, Szmigielska, A, Zaniew, M, Darlow, J M, Puri, P, Barton, D, Casolari, E, Furth, S L, Warady, B A, Gucev, Z, Hakonarson, H, Flogelova, H, Tasic, V, Latos-Bielenska, A, Materna-Kiryluk, A, Allegri, L, Wong, C S, Drummond, I A, D'Agati, V, Imamoto, A, Barasch, J M, Hildebrandt, F, Kiryluk, K, Lifton, R P, Morrow, B E, Jeanpierre, C, Papaioannou, V E, Ghiggeri, G M, Gharavi, A G, Katsanis, N & Sanna-Cherchi, S 2017, ' Genetic drivers of kidney defects in the digeorge syndrome ', New England Journal of Medicine, vol. 376, no. 8, pp. 742-754 . https://doi.org/10.1056/NEJMoa1609009
New England Journal of Medicine
New England Journal of Medicine, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
New England Journal of Medicine, Massachusetts Medical Society, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
The New England journal of medicine
376 (2017): 742–754. doi:10.1056/NEJMoa1609009
info:cnr-pdr/source/autori:Lopez-Rivera, E.; Liu, Y. P.; Verbitsky, M.; Anderson, B. R.; Capone, V. P.; Otto, E. A.; Yan, Z.; Mitrotti, A.; Martino, J.; Steers, N. J.; Fasel, D. A.; Vukojevic, K.; Deng, R.; Racedo, S. E.; Liu, Q.; Werth, M.; Westland, R.; Vivante, A.; Makar, G. S.; Bodria, M.; Sampson, M. G.; Gillies, C. E.; Vega-Warner, V.; Maiorana, M.; Petrey, D. S.; Honig, B.; Lozanovski, V. J.; Salomon, R.; Heidet, L.; Carpentier, W.; Gaillard, D.; Carrea, A.; Gesualdo, L.; Cusi, D.; Izzi, C.; Scolari, F.; van Wijk, J. A. E.; Arapovic, A.; Saraga-Babic, M.; Saraga, M.; Kunac, N.; Samii, A.; McDonald-McGinn, D. M.; Crowley, T. B.; Zackai, E. H.; Drozdz, D.; Miklaszewska, M.; Tkaczyk, M.; Sikora, P.; Szczepanska, M.; Mizerska-Wasiak, M.; Krzemien, G.; Szmigielska, A.; Zaniew, M.; Darlow, J. M.; Puri, P.; Barton, D.; Casolari, E.; Furth, S. L.; Warady, B. A.; Gucev, Z.; Hakonarson, H.; Flogelova, H.; Tasic, V.; Latos-Bielenska, A.; Materna-Kiryluk, A.; Allegri, L.; Wong, C. S.; Drummond, I. A.; D'Agati, V.; Imamoto, A.; Barasch, J. M.; Hildebrandt, F.; Kiryluk, K.; Lifton, R. P.; Morrow, B. E.; Jeanpierre, C.; Papaioannou, V. E.; Ghiggeri, G. M.; Gharavi, A. G.; Katsanis, N.; Sanna-Cherchi, S./titolo:Genetic Drivers of Kidney Defects in the DiGeorge Syndrome/doi:10.1056%2FNEJMoa1609009/rivista:The New England journal of medicine (Print)/anno:2017/pagina_da:742/pagina_a:754/intervallo_pagine:742–754/volume:376
Lopez-Rivera, E, Liu, Y P, Verbitsky, M, Anderson, B R, Capone, V P, Otto, E A, Yan, Z, Mitrotti, A, Martino, J, Steers, N J, Fasel, D A, Vukojevic, K, Deng, R, Racedo, S E, Liu, Q, Werth, M, Westland, R, Vivante, A, Makar, G S, Bodria, M, Sampson, M G, Gillies, C E, Vega-Warner, V, Maiorana, M, Petrey, D S, Honig, B, Lozanovski, V J, Salomon, R, Heidet, L, Carpentier, W, Gaillard, D, Carrea, A, Gesualdo, L, Cusi, D, Izzi, C, Scolari, F, Van Wijk, J A E, Arapovic, A, Saraga-Babic, M, Saraga, M, Kunac, N, Samii, A, McDonald-McGinn, D M, Crowley, T B, Zackai, E H, Drozdz, D, Miklaszewska, M, Tkaczyk, M, Sikora, P, Szczepanska, M, Mizerska-Wasiak, M, Krzemien, G, Szmigielska, A, Zaniew, M, Darlow, J M, Puri, P, Barton, D, Casolari, E, Furth, S L, Warady, B A, Gucev, Z, Hakonarson, H, Flogelova, H, Tasic, V, Latos-Bielenska, A, Materna-Kiryluk, A, Allegri, L, Wong, C S, Drummond, I A, D'Agati, V, Imamoto, A, Barasch, J M, Hildebrandt, F, Kiryluk, K, Lifton, R P, Morrow, B E, Jeanpierre, C, Papaioannou, V E, Ghiggeri, G M, Gharavi, A G, Katsanis, N & Sanna-Cherchi, S 2017, ' Genetic drivers of kidney defects in the digeorge syndrome ', New England Journal of Medicine, vol. 376, no. 8, pp. 742-754 . https://doi.org/10.1056/NEJMoa1609009
New England Journal of Medicine
New England Journal of Medicine, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
New England Journal of Medicine, Massachusetts Medical Society, 2017, 376 (8), pp.742-754. ⟨10.1056/NEJMoa1609009⟩
The New England journal of medicine
376 (2017): 742–754. doi:10.1056/NEJMoa1609009
info:cnr-pdr/source/autori:Lopez-Rivera, E.; Liu, Y. P.; Verbitsky, M.; Anderson, B. R.; Capone, V. P.; Otto, E. A.; Yan, Z.; Mitrotti, A.; Martino, J.; Steers, N. J.; Fasel, D. A.; Vukojevic, K.; Deng, R.; Racedo, S. E.; Liu, Q.; Werth, M.; Westland, R.; Vivante, A.; Makar, G. S.; Bodria, M.; Sampson, M. G.; Gillies, C. E.; Vega-Warner, V.; Maiorana, M.; Petrey, D. S.; Honig, B.; Lozanovski, V. J.; Salomon, R.; Heidet, L.; Carpentier, W.; Gaillard, D.; Carrea, A.; Gesualdo, L.; Cusi, D.; Izzi, C.; Scolari, F.; van Wijk, J. A. E.; Arapovic, A.; Saraga-Babic, M.; Saraga, M.; Kunac, N.; Samii, A.; McDonald-McGinn, D. M.; Crowley, T. B.; Zackai, E. H.; Drozdz, D.; Miklaszewska, M.; Tkaczyk, M.; Sikora, P.; Szczepanska, M.; Mizerska-Wasiak, M.; Krzemien, G.; Szmigielska, A.; Zaniew, M.; Darlow, J. M.; Puri, P.; Barton, D.; Casolari, E.; Furth, S. L.; Warady, B. A.; Gucev, Z.; Hakonarson, H.; Flogelova, H.; Tasic, V.; Latos-Bielenska, A.; Materna-Kiryluk, A.; Allegri, L.; Wong, C. S.; Drummond, I. A.; D'Agati, V.; Imamoto, A.; Barasch, J. M.; Hildebrandt, F.; Kiryluk, K.; Lifton, R. P.; Morrow, B. E.; Jeanpierre, C.; Papaioannou, V. E.; Ghiggeri, G. M.; Gharavi, A. G.; Katsanis, N.; Sanna-Cherchi, S./titolo:Genetic Drivers of Kidney Defects in the DiGeorge Syndrome/doi:10.1056%2FNEJMoa1609009/rivista:The New England journal of medicine (Print)/anno:2017/pagina_da:742/pagina_a:754/intervallo_pagine:742–754/volume:376
International audience; Background: The DiGeorge syndrome, the most common of the microdeletion syndromes, affects multiple organs, including the heart, the nervous system, and the kidney. It is caused by deletions on chromosome 22q11.2; the genetic
Autor:
Giovanni Montini, Monica Bodria, Alberto Edefonti, Francesco Scolari, Daniel A. Muruve, Alessia Fornoni, Felice Sica, Augusto Vaglio, Alberto Magnasco, Davide Martorana, Pietro Ravani, Luciana Ghio, Gianluca Caridi, Changli Wei, Gian Marco Ghiggeri, Jochen Reiser, Sandra Merscher-Gomez, Mirco Belingheri, Corrado Murtas, Andrea Pasini, Alessandro Ponticelli, Chiara Siciliano, Xiangyu Wang, Antonello Pani
Publikováno v:
Kidney international. 84(5)
In children with idiopathic nephrotic syndrome, rituximab can maintain short-term remission with withdrawal of prednisone and calcineurin inhibitors. Long-term effects including the number of repeated infusions to maintain remission are unknown. To t
Autor:
Francesco Scolari, Pietro Maffei, Vera Bettini, Ilaria Tosetto, Claudio Pagano, Nicola Sicolo, Jürgen K. Naggert, Richard B Paisey, Gabriella Milan, Roberto Vettor, Sara Romano, Francesca Favaretto, Nella Augusta Greggio, Jan D. Marshall
Alström syndrome (ALMS) is a rare autosomal recessive monogenic disease associated with obesity, hyperinsulinemia, and alterations of glucose metabolism that often lead to the development of type 2 diabetes at a young age.To study the relationship b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aeb81c57516702442b91a975166820a
http://hdl.handle.net/11577/2478286
http://hdl.handle.net/11577/2478286
Autor:
Gabriella Milan, Regina Tardanico, Alessandra Marega, Claudia Izzi, Francesco Scolari, Pietro Maffei, Jan D. Marshall, Paolo Foini
A 49-year-old woman was admitted with chronic renal failure. Prior history included poor vision, with development of photophobia at 3 years. Retinitis pigmentosa was documented, resulting in legal blindness by age 40. At the age of 20, sensorineural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7f34f041827caf190ac6a322f72cfe3
http://hdl.handle.net/11379/67853
http://hdl.handle.net/11379/67853
Publikováno v:
Heart International, Vol 2, Iss 3-4 (2006)
Heart International, Vol 2, Iss 3-4 (2009)
Heart International
Heart International, Vol 2, Iss 3-4 (2009)
Heart International
Cholesterol crystal embolism, known as atheroembolic disease, is caused by showers of cholesterol crystals from an atherosclerotic plaque that occludes small arteries. Embolization can occur spontaneously or as an iatrogenic complication from an inva