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Regional digitalisation in Europe: Institutional, cohesion-policy and innovation conditions in a spatial framework 1-gen-2026 Colamartino, Chiara; Barone, Marco; Bussoli, Candida; Toma, Pierluigi
The complement system in the pathogenesis and progression of kidney diseases: What doesn’t kill you makes you older 1-gen-2024 Stea, Ed; D'Ettorre, G; Mitrotti, A; Gesualdo, L
Rituximab in Granulomatosis with Polyangiotis: Challenging equilibrium between Therapeutic efficacy and iatrogenic complications 1-gen-2014 Mitrotti, A; L., Rossi; F., Indrio; M., Rossini; Di Palma, A. M.; L., Gesualdo; V., Montinaro.
Podocytes: the role of lysosomes in the development of nephrotic syndrome 1-gen-2020 Giliberti, Marica; Mitrotti, Adele; Gesualdo, Loreto
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations 1-gen-2017 Sanna-Cherchi, Simone; Khan, Kamal; Westland, Rik; Krithivasan, Priya; Fievet, Lorraine; Rasouly, Hila Milo; Ionita-Laza, Iuliana; Capone, Valentina P.; Fasel, David A.; Kiryluk, Krzysztof; Kamalakaran, Sitharthan; Bodria, Monica; Otto, Edgar A.; Sampson, Matthew G.; Gillies, Christopher E.; Vega-Warner, Virginia; Vukojevic, Katarina; Pediaditakis, Igor; Makar, Gabriel S.; Mitrotti, Adele; Verbitsky, Miguel; Martino, Jeremiah; Liu, Qingxue; Na, Young-Ji; Goj, Vinicio; Ardissino, Gianluigi; Gigante, Maddalena; Gesualdo, Loreto; Janezcko, Magdalena; Zaniew, Marcin; Mendelsohn, Cathy Lee; Shril, Shirlee; Hildebrandt, Friedhelm; Van Wijk, Joanna A E; Arapovic, Adela; Saraga, Marijan; Allegri, Landino; Izzi, Claudia; Scolari, Francesco; Tasic, Velibor; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Kiryluk, Anna-Materna; Mane, Shrikant; Goldstein, David B.; Lifton, Richard P.; Katsanis, Nicholas; Davis, Erica E.; Gharavi, Ali G.
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis 1-gen-2026 Wongboonsin, Janewit; Gibson, Kristen M.; Ke, Juntao; Sentell, Zachary T.; Arcila-Galvis, Juliana E.; Koyama, Satoshi; Greenberg, Anya; Reynolds, Kaylia M.; Montini, Giovanni; Magistroni, Riccardo; Mitrotti, Adele; Gesualdo, Loreto; Pezzuto, Alessandro; Peruzzi, Licia; Caliskan, Yasar; Onuchic-Whitford, Ana C.; Bunlungsup, Srichan; Mcnulty, Michelle; Gbadegesin, Rasheed; Saleem, Moin A.; Pollak, Martin R.; Hildebrandt, Friedhelm; Natarajan, Pradeep; Lee, Dongwon; Nigwekar, Sagar U.; Sayer, John A.; Sanna-Cherchi, Simone; Sampson, Matthew G.
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy 1-gen-2025 Wooden, Benjamin; Beenken, Andrew; Martinelli, Elena; Saida, Ken; Knob, Andrea L.; Ke, Juntao; Pisani, Isabella; Jin, Gina; Lane, Brandon; Mitrotti, Adele; Colby, Elizabeth; Lim, Tze Y.; Guglielmi, Francesca; Osborne, Amy J.; Ahram, Dina F.; Wang, Chen; Armand, Farid; Zanoni, Francesca; Bomback, Andrew S.; Delsante, Marco; Appel, Gerald B.; Ferrari, Massimo R. A.; Martino, Jeremiah; Sahdeo, Sunil; Breckenridge, David; Petrovski, Slavé; Paul, Dirk S.; Hall, Gentzon; Magistroni, Riccardo; Murtas, Corrado; Feriozzi, Sandro; Rampino, Teresa; Esposito, Pasquale; Helmuth, Margaret E.; Sampson, Matthew G.; Kretzler, Matthias; Kiryluk, Krzysztof; Shril, Shirlee; Gesualdo, Loreto; Maggiore, Umberto; Fiaccadori, Enrico; Gbadegesin, Rasheed; Santoriello, Dominick; D'Agati, Vivette D.; Saleem, Moin A.; Gharavi, Ali G.; Hildebrandt, Friedhelm; Pollak, Martin R.; Goldstein, David B.; Sanna-Cherchi, Simone
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes 1-gen-2025 Milo Rasouly, Hila; Krishna Murthy, Sarath Babu; Vena, Natalie; Povysil, Gundula; Beenken, Andrew; Verbitsky, Miguel; Shril, Shirlee; Lekkerkerker, Iris; Yang, Sandy; Khan, Atlas; Fasel, David; Wongboonsin, Janewit; Martino, Jeremiah; Ke, Juntao; Elefant, Naama; Tomar, Nikita; Harnof, Ofek; Kisselev, Sergey; Bheda, Shiraz; Reytan-Miron, Sivan; Lim, Tze Y.; Jamry-Dziurla, Anna; Lugani, Francesca; Zhang, Jun Y.; Marasa, Maddalena; Kolupaeva, Victoria; Groopman, Emily E.; Jin, Gina; Ghavami, Iman; Stevens, Kelsey O.; Coughlin, Arielle C.; Kil, Byum Hee; Chatterjee, Debanjana; Bradbury, Drew; Zheng, Jason; Mehl, Karla; Morban, Maria; Reingold, Rachel; Piva, Stacy; Mu, Xueru; Mitrotti, Adele; Szmigielska, Agnieszka; Gliwińska, Aleksandra; Ranghino, Andrea; Bomback, Andrew S.; Badenski, Andrzej; Latos-Bielenska, Anna; Capone, Valentina; Materna-Kiryluk, Anna; Amoroso, Antonio; Izzi, Claudia; La Scola, Claudio; Cohen, David Jonathan; Santoro, Domenico; Drozdz, Dorota; Fiaccadori, Enrico; Lin, Fangming; Scolari, Francesco; Tondolo, Francesco; La Manna, Gaetano; Appel, Gerald B.; Ghiggeri, Gian Marco; Zaza, Gianluigi; Montini, Giovanni; Masnata, Giuseppe; Krzemien, Grażyna; Pisani, Isabella; Radhakrishnan, Jai; Zachwieja, Katarzyna; Gesualdo, Loreto; Biancone, Luigi; Meneghesso, Davide; Mizerska-Wasiak, Malgorzata; Tkaczyk, Marcin; Zaniew, Marcin; Borszewska-Kornacka, Maria K.; Szczepanska, Maria; Saraga, Marijan; Rao, Maya K.; Bodria, Monica; Miklaszewska, Monika; Uy, Natalie S.; Baraldi, Olga; Bjanid, Omar; Esposito, Pasquale; Zamboli, Pasquale; Marzuillo, Pierluigi; Canetta, Pietro A.; Sikora, Przemyslaw; Westland, Rik; Crew, Russell J.; Alam, Shumyle; Guarino, Stefano; Negrisolo, Susanna; Hays, Thomas; Mane, Shrikant; Grandinetti, Valeria; Tasic, Velibor; Lozanovski, Vladimir J.; Caliskan, Yasar; Goldstein, David; Lifton, Richard P.; Ionita-Laza, Iuliana; Kiryluk, Krzysztof; Van Eerde, Albertien M.; Hildebrandt, Friedhelm; Sanna-Cherchi, Simone; Gharavi, Ali G.
Sindrome nefrosica e insufficienza renale rapidamente progressiva in paziente con componente monoclonale: un caso clinico 1-gen-2026 Lopez, Claudia; Mitrotti, Adele; Gesualdo, Loreto
Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis? 1-gen-2024 Mitrotti, Adele; Giliberti, Marica; Di Leo, Vincenzo; Di Bari, Ighli; Pontrelli, Paola; Gesualdo, Loreto
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome 1-gen-2017 Lopez Rivera, Esther; Liu, Yangfan P; Verbitsky, Miguel; Anderson, Blair R; Capone, Valentina P; Otto, Edgar A; Yan, Zhonghai; Mitrotti, Adele; Martino, Jeremiah; Steers, Nicholas J; Fasel, David A; Vukojevic, Katarina; Deng, Rong; Racedo, Silvia E; Liu, Qingxue; Werth, Max; Westland, Rik; Vivante, Asaf; Makar, Gabriel S; Bodria, Monica; Sampson, Matthew G; Gillies, Christopher E; Vega Warner, Virginia; Maiorana, Mariarosa; Petrey, Donald S; Honig, Barry; Lozanovski, Vladimir J; Salomon, Rémi; Heidet, Laurence; Carpentier, Wassila; Gaillard, Dominique; Carrea, Alba; Gesualdo, Loreto; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; Van Wijk, Joanna A. E; Arapovic, Adela; Saraga Babic, Mirna; Saraga, Marijan; Kunac, Nenad; Samii, Ali; Mcdonald Mcginn, Donna M; Crowley, Terrence B; Zackai, Elaine H; Drozdz, Dorota; Miklaszewska, Monika; Tkaczyk, Marcin; Sikora, Przemyslaw; Szczepanska, Maria; Mizerska Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Darlow, John M; Puri, Prem; Barton, David; Casolari, Emilio; Furth, Susan L; Warady, Bradley A; Gucev, Zoran; Hakonarson, Hakon; Flogelova, Hana; Tasic, Velibor; Latos Bielenska, Anna; Materna Kiryluk, Anna; Allegri, Landino; Wong, Craig S; Drummond, Iain A; D'Agati, Vivette; Imamoto, Akira; Barasch, Jonathan M; Hildebrandt, Friedhelm; Kiryluk, Krzysztof; Lifton, Richard P; Morrow, Bernice E; Jeanpierre, Cecile; Papaioannou, Virginia E; Ghiggeri, Gian Marco; Gharavi, Ali G; Katsanis, Nicholas; Sanna Cherchi, Simone
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy 1-gen-2024 Benjamin, Wooden; Andrew, Beenken; Elena, Martinelli; Ken, Saida; Andrea, L Knob; Juntao, Ke; Isabella, Pisani; Gina, Jin; Brandon, Lane; Mitrotti, A; Elizabeth, Colby; Tze, Y Lim; Francesca, Guglielmi; Amy, J Osborne; Dina, F Ahram; Chen, Wang; Farid, Armand; Francesca, Zanoni; Andrew, S Bomback; Marco, Delsante; Gerald, B Appel; Massimo R, A Ferrari; Jeremiah, Martino; Sunil, Sahdeo; David, Breckenridge; Slavé, Petrovski; Dirk, S Paul; Gentzon, Hall; Riccardo, Magistroni; Corrado, Murtas; Sandro, Feriozzi; Teresa, Rampino; Pasquale, Esposito; Margaret, E Helmuth; Matthew, G Sampson; Matthias, Kretzler; Krzysztof, Kiryluk; Shirlee, Shril; Loreto, Gesualdo; Umberto, Maggiore; Enrico, Fiaccadori; Rasheed, Gbadegesin; Dominick, Santoriello; Vivette, D D'Agati; Moin, A Saleem; Ali, G Gharavi; Friedhelm, Hildebrandt; Martin, R Pollak; David, B Goldstein; Simone, Sanna-Cherchi
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis 1-gen-2021 Weng, Pl; Majmundar, Aj; Khan, K; Lim, Ty; Shril, S; Jin, G; Musgrove, J; Wang, M; Ahram, Df; Aggarwal, Vs; Bier, Le; Heinzen, El; Onuchic-Whitford, Ac; Mann, N; Buerger, F; Schneider, R; Deutsch, K; Kitzler, Tm; Klämbt, V; Kolb, A; Mao, Y; Moufawad El Achkar, C; Mitrotti, A; Martino, J; Beck, Bb; Altmüller, J; Benz, Mr; Yano, S; Mikati, Ma; Gunduz, T; Cope, H; Shashi, V; Undiagnosed Diseases, Network; Trachtman, H; Bodria, M; Caridi, G; Pisani, I; Fiaccadori, E; Abumaziad, As; Martinez-Agosto, Ja; Yadin, O; Zuckerman, J; Kim, A; Ucla Clinical Genomics, Center; John-Kroegel, U; Tyndall, Av; Parboosingh, Js; Innes, Am; Bierzynska, A; Koziell, Ab; Muorah, M; Saleem, Ma; Hoefele, J; Riedhammer, Km; Gharavi, Ag; Jobanputra, V; Pierce-Hoffman, E; Seaby, Eg; O'Donnell-Luria, A; Rehm, Hl; Mane, S; D'Agati, Vd; Pollak, Mr; Ghiggeri, Gm; Lifton, Rp; Goldstein, Db; Davis, Ee; Hildebrandt, F; Sanna-Cherchi, S.
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome 1-gen-2023 Barry, Alexandra; Mcnulty, Michelle T; Jia, Xiaoyuan; Gupta, Yask; Debiec, Hanna; Luo, Yang; Nagano, China; Horinouchi, Tomoko; Jung, Seulgi; Colucci, Manuela; Ahram, Dina F; Mitrotti, Adele; Sinha, Aditi; Teeninga, Nynke; Jin, Gina; Shril, Shirlee; Caridi, Gianluca; Bodria, Monica; Lim, Tze Y; Westland, Rik; Zanoni, Francesca; Marasa, Maddalena; Turudic, Daniel; Giordano, Mario; Gesualdo, Loreto; Magistroni, Riccardo; Pisani, Isabella; Fiaccadori, Enrico; Reiterova, Jana; Maringhini, Silvio; Morello, William; Montini, Giovanni; Weng, Patricia L; Scolari, Francesco; Saraga, Marijan; Tasic, Velibor; Santoro, Domenica; Van Wijk, Joanna A E; Milošević, Danko; Kawai, Yosuke; Kiryluk, Krzysztof; Pollak, Martin R; Gharavi, Ali; Lin, Fangmin; Simœs E Silva, Ana Cristina; Loos, Ruth J F; Kenny, Eimear E; Schreuder, Michiel F; Zurowska, Aleksandra; Dossier, Claire; Ariceta, Gema; Drozynska-Duklas, Magdalena; Hogan, Julien; Jankauskiene, Augustina; Hildebrandt, Friedhelm; Prikhodina, Larisa; Song, Kyuyoung; Bagga, Arvind; Cheong, Hae; Ghiggeri, Gian Marco; Vachvanichsanong, Prayong; Nozu, Kandai; Lee, Dongwon; Vivarelli, Marina; Raychaudhuri, Soumya; Tokunaga, Katsushi; Sanna-Cherchi, Simone; Ronco, Pierre; Iijima, Kazumoto; Sampson, Matthew G
Diagnostic Utility of Exome Sequencing for Kidney Disease 1-gen-2019 Groopman, Ee; Marasa, M; Cameron-Christie, S; Petrovski, S; Aggarwal, Vs; Milo-Rasouly, H; Li, Y; Zhang, J; Nestor, J; Krithivasan, P; Lam, Wy; Mitrotti, A; Piva, S; Kil, Bh; Chatterjee, D; Reingold, R; Bradbury, D; Divecchia, M; Snyder, H; Mu, X; Mehl, K; Balderes, O; Fasel, Da; Weng, C; Radhakrishnan, J; Canetta, P; Appel, Gb; Bomback, As; Ahn, W; Uy, Ns; Alam, S; Cohen, Dj; Crew, Rj; Dube, Gk; Rao, Mk; Kamalakaran, S; Copeland, B; Ren, Z; Bridgers, J; Malone, Cd; Mebane, Cm; Dagaonkar, N; Fellström, Bc; Haefliger, C; Mohan, S; Sanna-Cherchi, S; Kiryluk, K; Fleckner, J; March, R; Platt, A; Goldstein, Db; Gharavi, Ag
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease 1-gen-2023 Gupta, Yask; Friedman, David J.; Mcnulty, Michelle T.; Khan, Atlas; Lane, Brandon; Wang, Chen; Ke, Juntao; Jin, Gina; Wooden, Benjamin; Knob, Andrea L.; Lim, Tze Y.; Appel, Gerald B.; Huggins, Kinsie; Liu, Lili; Mitrotti, Adele; Stangl, Megan C.; Bomback, Andrew; Westland, Rik; Bodria, Monica; Marasa, Maddalena; Shang, Ning; Cohen, David J.; Crew, Russell J.; Morello, William; Canetta, Pietro; Radhakrishnan, Jai; Martino, Jeremiah; Liu, Qingxue; Chung, Wendy K.; Espinoza, Angelica; Luo, Yuan; Wei, Wei-Qi; Feng, Qiping; Weng, Chunhua; Fang, Yilu; Kullo, Iftikhar J.; Naderian, Mohammadreza; Limdi, Nita; Irvin, Marguerite R.; Tiwari, Hemant; Mohan, Sumit; Rao, Maya; Dube, Geoffrey K.; Chaudhary, Ninad S.; Gutiérrez, Orlando M.; Judd, Suzanne E.; Cushman, Mary; Lange, Leslie A.; Lange, Ethan M.; Bivona, Daniel L.; Verbitsky, Miguel; Winkler, Cheryl A.; Kopp, Jeffrey B.; Santoriello, Dominick; Batal, Ibrahim; Pinheiro, Sérgio Veloso Brant; Oliveira, Eduardo Araújo; Simoes E Silva, Ana Cristina; Pisani, Isabella; Fiaccadori, Enrico; Lin, Fangming; Gesualdo, Loreto; Amoroso, Antonio; Ghiggeri, Gian Marco; D’Agati, Vivette D.; Magistroni, Riccardo; Kenny, Eimear E.; Loos, Ruth J. F.; Montini, Giovanni; Hildebrandt, Friedhelm; Paul, Dirk S.; Petrovski, Slavé; Goldstein, David B.; Kretzler, Matthias; Gbadegesin, Rasheed; Gharavi, Ali G.; Kiryluk, Krzysztof; Sampson, Matthew G.; Pollak, Martin R.; Sanna-Cherchi, Simone
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux 1-gen-2021 Verbitsky, Miguel; Krithivasan, Priya; Batourina, Ekaterina; Khan, Atlas; Graham, Sarah E; Marasà, Maddalena; Kim, Hyunwoo; Lim, Tze Y; Weng, Patricia L; Sánchez-Rodríguez, Elena; Mitrotti, Adele; Ahram, Dina F; Zanoni, Francesca; Fasel, David A; Westland, Rik; Sampson, Matthew G; Zhang, Jun Y; Bodria, Monica; Kil, Byum Hee; Shril, Shirlee; Gesualdo, Loreto; Torri, Fabio; Scolari, Francesco; Izzi, Claudia; Van Wijk, Joanna A E; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Barton, David E; Dobson, Mark G; Puri, Prem; Furth, Susan L; Warady, Bradley A; Pisani, Isabella; Fiaccadori, Enrico; Allegri, Landino; Degl'Innocenti, Maria Ludovica; Piaggio, Giorgio; Alam, Shumyle; Gigante, Maddalena; Zaza, Gianluigi; Esposito, Pasquale; Lin, Fangming; Simões-E-Silva, Ana Cristina; Brodkiewicz, Andrzej; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Szczepanska, Maria; Adamczyk, Piotr; Tkaczyk, Marcin; Tomczyk, Daria; Sikora, Przemyslaw; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Lozanovski, Vladimir J; Gucev, Zoran; Ionita-Laza, Iuliana; Stanaway, Ian B; Crosslin, David R; Wong, Craig S; Hildebrandt, Friedhelm; Barasch, Jonathan; Kenny, Eimear E; Loos, Ruth J F; Levy, Brynn; Ghiggeri, Gian Marco; Hakonarson, Hakon; Latos-Bieleńska, Anna; Materna-Kiryluk, Anna; Darlow, John M; Tasic, Velibor; Willer, Cristen; Kiryluk, Krzysztof; Sanna-Cherchi, Simone; Mendelsohn, Cathy L; Gharavi, Ali G
DUPLICATION OF THE SOX3 GENE IN AN SRY-NEGATIVE 46,XX MALE WITH ASSOCIATED CONGENITAL ANOMALIES OF KIDNEYS AND THE URINARY TRACT: CASE REPORT AND REVIEW OF THE LITERATURE 1-gen-2019 Tasic, V; Mitrotti, A; Riepe, Fg; Kulle, Ae; Laban, N; Polenakovic, M; Plaseska-Karanfilska, D; Sanna-Cherchi, S; Kostovski, M; Gucev, Z
The copy number variation landscape of congenital anomalies of the kidney and urinary tract 1-gen-2019 Verbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasà, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; Van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmoliński, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cécile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Débora M.; Oliveira, Eduardo A.; Simões-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone
The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing 1-gen-2019 Rasouly, Hm; Groopman, Ee; Heyman-Kantor, R; Fasel, Da; Mitrotti, A; Westland, R; Bier, L; Weng, C; Ren, Z; Copeland, B; Krithivasan, P; Chung, Wk; Sanna-Cherchi, S; Goldstein, Db; Gharavi, Ag
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Tipologia
  • 1 Contributo su Rivista10319
Autore
  • IACOVIELLO, LICIA757
  • ILICETO, SABINO527
  • CASTELLANI, DANIELE324
  • MAGAZZINO, COSIMO260
  • COLOSIMO, CARLO253
  • CORMIO, LUIGI242
  • PICCA, ANNA233
  • ROCCA, BIANCA231
  • MEMEO, RICCARDO226
  • TROIANO, GIUSEPPE219
Data di pubblicazione
  • In corso di stampa26
  • 2020 - 20264730
  • 2010 - 20193821
  • 2000 - 20091292
  • 1990 - 1999374
  • 1980 - 198975
  • 1977 - 19791
Rivista
  • INTERNATIONAL JOURNAL OF MOLECULA...116
  • JOURNAL OF CLINICAL MEDICINE104
  • PLOS ONE80
  • EUROPEAN HEART JOURNAL70
  • CANCERS69
  • NUTRIENTS67
  • SCIENTIFIC REPORTS63
  • THROMBOSIS AND HAEMOSTASIS60
  • MOVEMENT DISORDERS56
  • NMCD. NUTRITION METABOLISM AND CA...56
Keyword
  • Humans320
  • Male155
  • Female148
  • COVID-19128
  • Aged108
  • Italy99
  • Middle Aged99
  • Cardiology and Cardiovascular Med...88
  • Adult85
  • Medicine (all)62
Lingua
  • eng6474
  • ita941
  • fre12
  • spa12
  • ger3
  • und2
  • afr1
  • bul1
  • lat1
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