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Titolo Data di pubblicazione Autore(i) File
Genetically Determined Interaction between the Dopamine Transporter and the D-2 Receptor on Prefronto-Striatal Activity and Volume in Humans 1-gen-2009 Bertolino, A; Fazio, L; Di Giorgio, A; Blasi, G; Romano, R; Taurisano, P; Caforio, G; Sinibaldi, L; Ursini, G; Popolizio, T; Tirotta, E; Papp, A; Dallapiccola, B; Borrelli, E; Sadee, W
Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans 1-gen-2009 Bertolino, Alessandro; Fazio, Leonardo; DI GIORGIO, Annabella; Blasi, Giuseppe; Romano, Raffaella; Taurisano, Paolo; Caforio, Grazia; Sinibaldi, L.; Ursini, Gianluca; Popolizio, T.; Tirotta, E.; Papp, A.; Dallapiccola, B.; Borrelli, E.; Sadee, W.
Genetically Determined Measures of Striatal D2 Signaling Predict Prefrontal Activity during Working Memory Performance 1-gen-2010 Bertolino, A; Taurisano, P; Pisciotta, Nm; Blasi, G; Fazio, L; Romano, R; Gelao, B; Lo Bianco, L; Lozupone, M; Di Giorgio, A; Caforio, G; Sambataro, F; Niccoli-Asabella, A; Papp, A; Ursini, G; Sinibaldi, L; Popolizio, T; Sadee, W; Rubini, G
Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance 1-gen-2010 Bertolino, Alessandro; Taurisano, Paolo; Pisciotta, N. M; Blasi, Giuseppe; Fazio, Leonardo; Romano, Raffaella; Gelao, Barbara; LO BIANCO, Luciana; Lozupone, M.; DI GIORGIO, Annabella; Caforio, Grazia; Sambataro, F.; NICCOLI ASABELLA, Artor; Papp, A.; Ursini, Gianluca; Sinibaldi, L.; Popolizio, T.; Sadee, W.; Rubini, Giuseppe
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype 1-gen-2014 Ambrosini, E.; Sicca, F.; Brignone, M. S.; D'Adamo, Maria Cristina; Napolitano, C.; Servettini, Ilenio; Moro, F.; Guglielmi, L.; Pieroni, Stefania; Servillo, Giuseppe; Lanciotti, A.; Valvo, G.; Catacuzzeno, Luigi; Franciolini, Fabio; Molinari, P.; Marchese, M.; Grottesi, A.; Guerrini, R.; Santorelli, F. M.; Priori, S.; Pessia, Mauro
Genetics of irritable bowel syndrome 1-gen-2016 Henström, Maria; D’Amato, Mauro
Genetics of irritable bowel syndrome: shifting gear via biobank-scale studies 1-gen-2022 Camilleri, Michael; Zhernakova, Alexandra; Bozzarelli, Isotta; D'Amato, Mauro
Genocidio, Crimini di guerra, contro la pace, contro l'umanità 1-gen-2011 Depasquale, Patrizia
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people 1-gen-2022 Eising, E.; Mirza-Schreiber, N.; de Zeeuw, E. L.; Wang, C. A.; Truong, D. T.; Allegrini, A. G.; Shapland, C. Y.; Zhu, G.; Wigg, K. G.; Gerritse, M. L.; Molz, B.; Alagoz, G.; Gialluisi, A.; Abbondanza, F.; Rimfeld, K.; van Donkelaar, M.; Liao, Z.; Jansen, P. R.; Andlauer, T. F. M.; Bates, T. C.; Bernard, M.; Blokland, K.; Bonte, M.; Borglum, A. D.; Bourgeron, T.; Brandeis, D.; Ceroni, F.; Csepe, V.; Dale, P. S.; de Jong, P. F.; Defries, J. C.; Demonet, J. -F.; Demontis, D.; Feng, Y.; Gordon, S. D.; Guger, S. L.; Hayiou-Thomas, M. E.; Hernandez-Cabrera, J. A.; Hottenga, J. -J.; Hulme, C.; Kere, J.; Kerr, E. N.; Koomar, T.; Landerl, K.; Leonard, G. T.; Lovett, M. W.; Lyytinen, H.; Martin, N. G.; Martinelli, A.; Maurer, U.; Michaelson, J. J.; Moll, K.; Monaco, A. P.; Morgan, A. T.; Nothen, M. M.; Pausova, Z.; Pennell, C. E.; Pennington, B. F.; Price, K. M.; Rajagopal, V. M.; Ramus, F.; Richer, L.; Simpson, N. H.; Smith, S. D.; Snowling, M. J.; Stein, J.; Strug, L. J.; Talcott, J. B.; Tiemeier, H.; van der Schroeff, M. P.; Verhoef, E.; Watkins, K. E.; Wilkinson, M.; Wright, M. J.; Barr, C. L.; Boomsma, D. I.; Carreiras, M.; Franken, M. -C. J.; Gruen, J. R.; Luciano, M.; Muller-Myhsok, B.; Newbury, D. F.; Olson, R. K.; Paracchini, S.; Paus, T.; Plomin, R.; Reilly, S.; Schulte-Korne, G.; Tomblin, J. B.; van Bergen, E.; Whitehouse, A. J. O.; Willcutt, E. G.; St Pourcain, B.; Francks, C.; Fisher, S. E.
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders 1-gen-2021 Eijsbouts, Chris; Zheng, Tenghao; Kennedy, Nicholas A; Bonfiglio, Ferdinando; Anderson, Carl A; Moutsianas, Loukas; Holliday, Joanne; Shi, Jingchunzi; Shringarpure, Suyash; Voda, Alexandru-Ioan; Farrugia, Gianrico; Franke, Andre; Hübenthal, Matthias; Abecasis, Gonçalo; Zawistowski, Matthew; Skogholt, Anne Heidi; Ness-Jensen, Eivind; Hveem, Kristian; Esko, Tõnu; Teder-Laving, Maris; Zhernakova, Alexandra; Camilleri, Michael; Boeckxstaens, Guy; Whorwell, Peter J; Spiller, Robin; Mcvean, Gil; D'Amato, Mauro; Jostins, Luke; Parkes, Miles
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease 1-gen-2021 Zheng, Tenghao; Ellinghaus, David; Juzenas, Simonas; Cossais, François; Burmeister, Greta; Mayr, Gabriele; Jørgensen, Isabella Friis; Teder-Laving, Maris; Skogholt, Anne Heidi; Chen, Sisi; Strege, Peter R; Ito, Go; Banasik, Karina; Becker, Thomas; Bokelmann, Frank; Brunak, Søren; Buch, Stephan; Clausnitzer, Hartmut; Datz, Christian; Degenhardt, Frauke; Doniec, Marek; Erikstrup, Christian; Esko, Tõnu; Forster, Michael; Frey, Norbert; Fritsche, Lars G; Gabrielsen, Maiken Elvestad; Gräßle, Tobias; Gsur, Andrea; Gross, Justus; Hampe, Jochen; Hendricks, Alexander; Hinz, Sebastian; Hveem, Kristian; Jongen, Johannes; Junker, Ralf; Karlsen, Tom Hemming; Hemmrich-Stanisak, Georg; Kruis, Wolfgang; Kupcinskas, Juozas; Laubert, Tilman; Rosenstiel, Philip C; Röcken, Christoph; Laudes, Matthias; Leendertz, Fabian H; Lieb, Wolfgang; Limperger, Verena; Margetis, Nikolaos; Mätz-Rensing, Kerstin; Németh, Christopher Georg; Ness-Jensen, Eivind; Nowak-Göttl, Ulrike; Pandit, Anita; Pedersen, Ole Birger; Peleikis, Hans Günter; Peuker, Kenneth; Rodriguez, Cristina Leal; Rühlemann, Malte Christoph; Schniewind, Bodo; Schulzky, Martin; Skieceviciene, Jurgita; Tepel, Jürgen; Thomas, Laurent; Uellendahl-Werth, Florian; Ullum, Henrik; Vogel, Ilka; Volzke, Henry; von Fersen, Lorenzo; von Schönfels, Witigo; Vanderwerff, Brett; Wilking, Julia; Wittig, Michael; Zeissig, Sebastian; Zobel, Myrko; Zawistowski, Matthew; Vacic, Vladimir; Sazonova, Olga; Noblin, Elizabeth S; Farrugia, Gianrico; Beyder, Arthur; Wedel, Thilo; Kahlke, Volker; Schafmayer, Clemens; D'Amato, Mauro; Franke, Andre
Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota 1-gen-2016 Wang, Jun; Thingholm, Louise B; Skiecevičienė, Jurgita; Rausch, Philipp; Kummen, Martin; Hov, Johannes R; Degenhardt, Frauke; Heinsen, Femke-Anouska; Rühlemann, Malte C; Szymczak, Silke; Holm, Kristian; Esko, Tönu; Sun, Jun; Pricop-Jeckstadt, Mihaela; Al-Dury, Samer; Bohov, Pavol; Bethune, Jörn; Sommer, Felix; Ellinghaus, David; Berge, Rolf K; Hübenthal, Matthias; Koch, Manja; Schwarz, Karin; Rimbach, Gerald; Hübbe, Patricia; Pan, Wei-Hung; Sheibani-Tezerji, Raheleh; Häsler, Robert; Rosenstiel, Philipp; D'Amato, Mauro; Cloppenborg-Schmidt, Katja; Künzel, Sven; Laudes, Matthias; Marschall, Hanns-Ulrich; Lieb, Wolfgang; Nöthlings, Ute; Karlsen, Tom H; Baines, John F; Franke, Andre
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms 1-gen-2019 Schafmayer, Clemens; Harrison, James William; Buch, Stephan; Lange, Christina; Reichert, Matthias C; Hofer, Philipp; Cossais, François; Kupcinskas, Juozas; von Schönfels, Witigo; Schniewind, Bodo; Kruis, Wolfgang; Tepel, Jürgen; Zobel, Myrko; Rosendahl, Jonas; Jacobi, Thorsten; Walther-Berends, Andreas; Schroeder, Michael; Vogel, Ilka; Sergeev, Petr; Boedeker, Hans; Hinrichsen, Holger; Volk, Andreas; Erk, Jens-Uwe; Burmeister, Greta; Hendricks, Alexander; Hinz, Sebastian; Wolff, Sebastian; Böttner, Martina; Wood, Andrew R; Tyrrell, Jessica; Beaumont, Robin N; Langheinrich, Melanie; Kucharzik, Torsten; Brezina, Stefanie; Huber-Schönauer, Ursula; Pietsch, Leonora; Noack, Laura Sophie; Brosch, Mario; Herrmann, Alexander; Thangapandi, Raghavan Veera; Schimming, Hans Wolfgang; Zeissig, Sebastian; Palm, Stefan; Focke, Gerd; Andreasson, Anna; Schmidt, Peter T; Weitz, Juergen; Krawczak, Michael; Völzke, Henry; Leeb, Gernot; Michl, Patrick; Lieb, Wolfgang; Grützmann, Robert; Franke, Andre; Lammert, Frank; Becker, Thomas; Kupcinskas, Limas; D’Amato, Mauro; Wedel, Thilo; Datz, Christian; Gsur, Andrea; Weedon, Michael N; Hampe, Jochen
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia 1-gen-2019 Gialluisi, A; Andlauer, Tfm; Mirza-Schreiber, N; Moll, K; Becker, J; Hoffmann, P; Ludwig, Ku; Czamara, D; St Pourcain, B; Brandler, W; Honbolygó, F; Tóth, D; Csépe, V; Huguet, G; Morris, Ap; Hulslander, J; Willcutt, Eg; Defries, Jc; Olson, Rk; Smith, Sd; Pennington, Bf; Vaessen, A; Maurer, U; Lyytinen, H; Peyrard-Janvid, M; Leppänen, Pht; Brandeis, D; Bonte, M; Stein, Jf; Talcott, Jb; Fauchereau, F; Wilcke, A; Francks, C; Bourgeron, T; Monaco, Ap; Ramus, F; Landerl, K; Kere, J; Scerri, Ts; Paracchini, S; Fisher, Se; Schumacher, J; Nöthen, Mm; Müller-Myhsok, B; Schulte-Körne, G; Gialluisi, A; Andlauer, Tfm; Mirza-Schreiber, N; Moll, K; Becker, J; Hoffmann, P; Ludwig, Ku; Czamara, D; St Pourcain, B; Brandler, W; Honbolygó, F; Tóth, D; Csépe, V; Huguet, G; Morris, Ap; Hulslander, J; Willcutt, Eg; Defries, Jc; Olson, Rk; Smith, Sd; Pennington, Bf; Vaessen, A; Maurer, U; Lyytinen, H; Peyrard-Janvid, M; Leppänen, Pht; Brandeis, D; Bonte, M; Stein, Jf; Talcott, Jb; Fauchereau, F; Wilcke, A; Francks, C; Bourgeron, T; Monaco, Ap; Ramus, F; Landerl, K; Kere, J; Scerri, Ts; Paracchini, S; Fisher, Se; Schumacher, J; Nöthen, Mm; Müller-Myhsok, B; Schulte-Körne, G
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity 1-gen-2017 Joshi, Pk; Pirastu, N; Kentistou, Ka; Fischer, K; Hofer, E; Schraut, Ke; Clark, Dw; Nutile, T; Barnes, Clk; Timmers, Prhj; Shen, X; Gandin, I; Mcdaid, Af; Hansen, Tf; Gordon, Sd; Giulianini, F; Boutin, Ts; Abdellaoui, A; Zhao, W; Medina-Gomez, C; Bartz, Tm; Trompet, S; Lange, La; Raffield, L; van der Spek, A; Galesloot, Te; Proitsi, P; Yanek, Lr; Bielak, Lf; Payton, A; Murgia, F; Concas, Mp; Biino, G; Tajuddin, Sm; Seppälä, I; Amin, N; Boerwinkle, E; Børglum, Ad; Campbell, A; Demerath, Ew; Demuth, I; Faul, Jd; Ford, I; Gialluisi, A; Gögele, M; Graff, M; Hingorani, A; Hottenga, Jj; Hougaard, Dm; Hurme, Ma; Ikram, Ma; Jylhä, M; Kuh, D; Ligthart, L; Lill, Cm; Lindenberger, U; Lumley, T; Mägi, R; Marques-Vidal, P; Medland, Se; Milani, L; Nagy, R; Ollier, Wer; Peyser, Pa; Pramstaller, Pp; Ridker, Pm; Rivadeneira, F; Ruggiero, D; Saba, Y; Schmidt, R; Schmidt, H; Slagboom, Pe; Smith, Bh; Smith, Ja; Sotoodehnia, N; Steinhagen-Thiessen, E; van Rooij, Fja; Verbeek, Al; Vermeulen, Sh; Vollenweider, P; Wang, Y; Werge, T; Whitfield, Jb; Zonderman, Ab; Lehtimäki, T; Evans, Mk; Pirastu, M; Fuchsberger, C; Bertram, L; Pendleton, N; Kardia, Slr; Ciullo, M; Becker, Dm; Wong, A; Psaty, Bm; van Duijn, Cm; Wilson, Jg; Jukema, Jw; Kiemeney, L; Uitterlinden, Ag; Franceschini, N; North, Ke; Weir, Dr; Metspalu, A; Boomsma, Di; Hayward, C; Chasman, D; Martin, Ng; Sattar, N; Campbell, H; Esko, T; Kutalik, Z; Wilson, Jf.; Joshi, Pk; Pirastu, N; Kentistou, Ka; Fischer, K; Hofer, E; Schraut, Ke; Clark, Dw; Nutile, T; Barnes, Clk; Timmers, Prhj; Shen, X; Gandin, I; Mcdaid, Af; Hansen, Tf; Gordon, Sd; Giulianini, F; Boutin, Ts; Abdellaoui, A; Zhao, W; Medina-Gomez, C; Bartz, Tm; Trompet, S; Lange, La; Raffield, L; van der Spek, A; Galesloot, Te; Proitsi, P; Yanek, Lr; Bielak, Lf; Payton, A; Murgia, F; Concas, Mp; Biino, G; Tajuddin, Sm; Seppälä, I; Amin, N; Boerwinkle, E; Børglum, Ad; Campbell, A; Demerath, Ew; Demuth, I; Faul, Jd; Ford, I; Gialluisi, A; Gögele, M; Graff, M; Hingorani, A; Hottenga, Jj; Hougaard, Dm; Hurme, Ma; Ikram, Ma; Jylhä, M; Kuh, D; Ligthart, L; Lill, Cm; Lindenberger, U; Lumley, T; Mägi, R; Marques-Vidal, P; Medland, Se; Milani, L; Nagy, R; Ollier, Wer; Peyser, Pa; Pramstaller, Pp; Ridker, Pm; Rivadeneira, F; Ruggiero, D; Saba, Y; Schmidt, R; Schmidt, H; Slagboom, Pe; Smith, Bh; Smith, Ja; Sotoodehnia, N; Steinhagen-Thiessen, E; van Rooij, Fja; Verbeek, Al; Vermeulen, Sh; Vollenweider, P; Wang, Y; Werge, T; Whitfield, Jb; Zonderman, Ab; Lehtimäki, T; Evans, Mk; Pirastu, M; Fuchsberger, C; Bertram, L; Pendleton, N; Kardia, Slr; Ciullo, M; Becker, Dm; Wong, A; Psaty, Bm; van Duijn, Cm; Wilson, Jg; Jukema, Jw; Kiemeney, L; Uitterlinden, Ag; Franceschini, N; North, Ke; Weir, Dr; Metspalu, A; Boomsma, Di; Hayward, C; Chasman, D; Martin, Ng; Sattar, N; Campbell, H; Esko, T; Kutalik, Z; Wilson, Jf.
Genome-wide screening for DNA variants associated with reading and language traits 1-gen-2014 Gialluisi, A; Newbury, Df; Wilcutt, Eg; Olson, Rk; Defries, Jc; Brandler, Wm; Pennington, Bf; Smith, Sd; Scerri, Ts; Simpson, Nh; Sli, Consortium; Luciano, M; Evans DM, ; Bates, Tc; Stein, Jf; Talcott, Jb; Monaco, Ap; Paracchini, S; Francks, C; Fisher SE,
Genomewide Association Study of Severe Covid-19 with Respiratory Failure 1-gen-2020 Ellinghaus, David; Degenhardt, Frauke; Bujanda, Luis; Buti, Maria; Albillos, Agustín; Invernizzi, Pietro; Fernández, Javier; Prati, Daniele; Baselli, Guido; Asselta, Rosanna; Grimsrud, Marit M; Milani, Chiara; Aziz, Fátima; Kässens, Jan; May, Sandra; Wendorff, Mareike; Wienbrandt, Lars; Uellendahl-Werth, Florian; Zheng, Tenghao; Yi, Xiaoli; de Pablo, Raúl; Chercoles, Adolfo G; Palom, Adriana; Garcia-Fernandez, Alba-Estela; Rodriguez-Frias, Francisco; Zanella, Alberto; Bandera, Alessandra; Protti, Alessandro; Aghemo, Alessio; Lleo, Ana; Biondi, Andrea; Caballero-Garralda, Andrea; Gori, Andrea; Tanck, Anja; Carreras Nolla, Anna; Latiano, Anna; Fracanzani, Anna Ludovica; Peschuck, Anna; Julià, Antonio; Pesenti, Antonio; Voza, Antonio; Jiménez, David; Mateos, Beatriz; Nafria Jimenez, Beatriz; Quereda, Carmen; Paccapelo, Cinzia; Gassner, Christoph; Angelini, Claudio; Cea, Cristina; Solier, Aurora; Pestaña, David; Muñiz-Diaz, Eduardo; Sandoval, Elena; Paraboschi, Elvezia M; Navas, Enrique; García Sánchez, Félix; Ceriotti, Ferruccio; Martinelli-Boneschi, Filippo; Peyvandi, Flora; Blasi, Francesco; Téllez, Luis; Blanco-Grau, Albert; Hemmrich-Stanisak, Georg; Grasselli, Giacomo; Costantino, Giorgio; Cardamone, Giulia; Foti, Giuseppe; Aneli, Serena; Kurihara, Hayato; Elabd, Hesham; My, Ilaria; Galván-Femenia, Iván; Martín, Javier; Erdmann, Jeanette; Ferrusquía-Acosta, Jose; Garcia-Etxebarria, Koldo; Izquierdo-Sanchez, Laura; Bettini, Laura R; Sumoy, Lauro; Terranova, Leonardo; Moreira, Leticia; Santoro, Luigi; Scudeller, Luigia; Mesonero, Francisco; Roade, Luisa; Rühlemann, Malte C; Schaefer, Marco; Carrabba, Maria; Riveiro-Barciela, Mar; Figuera Basso, Maria E; Valsecchi, Maria G; Hernandez-Tejero, María; Acosta-Herrera, Marialbert; D'Angiò, Mariella; Baldini, Marina; Cazzaniga, Marina; Schulzky, Martin; Cecconi, Maurizio; Wittig, Michael; Ciccarelli, Michele; Rodríguez-Gandía, Miguel; Bocciolone, Monica; Miozzo, Monica; Montano, Nicola; Braun, Nicole; Sacchi, Nicoletta; Martínez, Nilda; Özer, Onur; Palmieri, Orazio; Faverio, Paola; Preatoni, Paoletta; Bonfanti, Paolo; Omodei, Paolo; Tentorio, Paolo; Castro, Pedro; Rodrigues, Pedro M; Blandino Ortiz, Aaron; de Cid, Rafael; Ferrer, Ricard; Gualtierotti, Roberta; Nieto, Rosa; Goerg, Siegfried; Badalamenti, Salvatore; Marsal, Sara; Matullo, Giuseppe; Pelusi, Serena; Juzenas, Simonas; Aliberti, Stefano; Monzani, Valter; Moreno, Victor; Wesse, Tanja; Lenz, Tobias L; Pumarola, Tomas; Rimoldi, Valeria; Bosari, Silvano; Albrecht, Wolfgang; Peter, Wolfgang; Romero-Gómez, Manuel; D'Amato, Mauro; Duga, Stefano; Banales, Jesus M; Hov, Johannes R; Folseraas, Trine; Valenti, Luca; Franke, Andre; Karlsen, Tom H
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase 1-gen-2012 Salvi, E; Kutalik, Z; Glorioso, N; Benaglio, P; Frau, F; Kuznetsova, T; Arima, H; Hoggart, C; Tichet, J; Nikitin, Yp; Conti, C; Seidlerova, J; Tikhonoff, V; Stolarz Skrzypek, K; Johnson, T; Devos, N; Zagato, L; Guarrera, S; Zaninello, R; Calabria, A; Stancanelli, B; Troffa, C; Thijs, L; Rizzi, F; Simonova, G; Lupoli, S; Argiolas, G; Braga, D; D'Alessio, Mc; Ortu, Mf; Ricceri, F; Mercurio, M; Descombes, P; Marconi, M; Chalmers, J; Harrap, S; Filipovsky, J; Bochud, M; Iacoviello, Licia; Ellis, J; Stanton, Av; Laan, M; Padmanabhan, S; Dominiczak, Af; Samani, Nj; Melander, O; Jeunemaitre, X; Manunta, P; Shabo, A; Vineis, P; Cappuccio, Fp; Caulfield, Mj; Matullo, G; Rivolta, C; Munroe, Pb; Barlassina, C; Staessen, Ja; Beckmann, Js; Cusi, D.
Genomic organization and cytokine-mediated inducibility of the human TRIM-8/GERP gene 1-gen-2004 Toniato, Elena; Flati, V; Laglia, E; Mincione, Gabriella; Martinotti, Stefano
Genomic overlap between age at onset of Parkinson Disease and blood platelet parameters variability 1-gen-2021 Tirozzi, Alfonsina; Parisi, Roberta; Cerletti, Chiara; Benedetta Donati, Maria; de Gaetano, Giovanni; Iacoviello, Licia; Gialluisi, Alessandro
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