Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vinicio Goj"'
Autor:
Antonella Talenti, Stefania Del Sesto, Laura Giordano, Anna Rita Benincaso, L Bernardo, Francesca Ferrara, Vinicio Goj, Paolo Antonio Ascierto, Piero Biondi, Antonella Grisolia
Publikováno v:
Drugs & Therapy Perspectives
Tocilizumab is one of the newest therapeutic options for the acute respiratory distress syndrome (ARDS) caused by the recently discovered severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) β-coronavirus. Several trials are currently ongoin
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:
Lorraine N. Clark, Krzysztof Kiryluk, Francesco Scolari, Gian Marco Ghiggeri, Marcin Zaniew, Anna Materna-Kiryluk, Valentina Corbani, Anita Ammenti, Stephen Sanders, Stefania Giberti, Hana Flögelová, Daniele Cusi, Ali G. Gharavi, Maddalena Gigante, Simona Curioni, Kristina Drnasin, Hakon Hakonarson, Akshata Kini, Landino Allegri, Simone Sanna-Cherchi, Roel Sterken, Luca Bernardo, Claudia Izzi, Nadica Ristoska-Bojkovska, Adela Arapović, Loreto Gesualdo, Brittany J. Perry, Sandosh Padmanabhan, Matthew W. State, Vladimir J Lozanovski, Alba Carrea, Cristina Barlassina, Dexter Hadley, Matthew G. Sampson, Richard P. Lifton, Tatiana Foroud, Wendy K. Chung, Gianluca Caridi, Miguel Verbitsky, Shannon N. Nees, Zoran Gucev, Nilgun Kacak, Marijan Saraga, Vinicio Goj, Katelyn Elizabeth Burgess, Velibor Tasic, Monica Bodria, Patricia L. Weng, Stefania Ferretti, Beatrice Bianco, Danio Somenzi, Corrado Murtas, Anna Latos-Bielenska, Vaidehi Jobanputra, Franca Allegri, Anna F. Dominiczak
Publikováno v:
American journal of human genetics, vol 91, iss 6
We examined the burden of large, rare, copy-number variants (CNVs) in 192 individuals with renal hypodysplasia (RHD) and replicated findings in 330 RHD cases from two independent cohorts. CNV distribution was significantly skewed toward larger gene-d
Autor:
G Marra, Baroukh M. Assael, Vinicio Goj, Carlo Alberto Dell Agnola, B. Tadini, G. Cavanna, Silvia A. Tirelli, Aldo Claris Appiani, Umberto Nicolini
Publikováno v:
The Journal of pediatrics. 110(6)
Renal function of 18 infants who had undergone surgery in the neonatal period because of severe congenital hydronephrosis was followed up for 5 to 36 months (mean +/- SD 21 +/- 10 months). In all cases the diagnosis was made prenatally by sonography