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Mostrati risultati da 11.773 a 11.792 di 31.841
Data di pubblicazione Titolo Autore(i) File
1-gen-2004 G20210A Prothrombin gene polymorphism and coronary ischaemic syndromes: A phenotype-specific meta-analysis of 12 034 subjects Burzotta, Francesco; Paciaroni, K.; De Stefano, Valerio; Crea, Filippo; Maseri, A.; Leone, Maria Grazia; Andreotti, Felicita
1-gen-2000 G20210A prothrombin gene polymorphism and extent of coronary disease Burzotta, Francesco; Paciaroni, Katia; Andreotti, Felicita; Casorelli, I; De Stefano, Valerio
1-gen-2004 G20210A prothrombin gene variant and clinical outcome in patients with a first acute coronary syndrome Burzotta, Francesco; Leone, Antonio Maria; Paciaroni, Katia; De Stefano, Valerio; Rossi, Elena; Testa, Luca; Giannico, Floriana; Leone, Giuseppe; Maseri, Attilio; Crea, Filippo; Andreotti, Felicita
1-gen-2000 The G20210A prothrombin mutation and the Physicians' Health Study Andreotti, F; Burzotta, F; De Stefano, V; Maseri, A; Iacoviello, L
1-gen-2004 G20210A protrombin gene variant and clinical outcome in patients with a first acute coronary syndrome Burzotta, Francesco; Leone, Antonio Maria; Paciaroni, Katia; De Stefano, Valerio; Rossi, Elena; Testa, Luca; Giannico, Floriana; Leone, Giuseppe; Maseri, Attilio; Crea, Filippo; Andreotti, Felicita
1-gen-2015 GABAB Agonists for the Treatment of Alcohol Use Disorder Mirijello, Antonio; Caputo, Francesco Maria; Vassallo, Gabriele Angelo; Gasbarrini, Antonio; Addolorato, Giovanni
1-gen-2012 Gabapentin as add-on treatment for somatoform disorder: a case report Guglielmo, Riccardo; Martinotti, Giovanni; Janiri, Luigi
1-gen-2000 Gabapentin in the prophylaxis of migraine: a double-blind randomized placebo-controlled study Mazza, Salvatore; Di Trapani, G; Mei, D; Marra, Camillo; Mazza, S; Capuano, A.
1-gen-2007 Gadobenate dimeglumine-enhanced MR angiography: Diagnostic performance of four doses for detection and grading of carotid, renal, and aorto-iliac stenoses compared to digital subtraction angiography Schneider, G; Ballarati, C; Grazioli, L; Manfredi, Riccardo; Thurnher, S; Kroencke, Tj; Taupitz, M; Merlino, Biagio; Bonomo, Lorenzo; Shen, N; Pirovano, G; Kirchin, Ma; Spinazzi, A.
1-gen-2010 Gadolinium enhancement of the lumbar leptomeninges and roots in a case of ALS Luigetti, Marco; Cianfoni, Alessandro; Conte, Amelia; Sabatelli, Mario
1-gen-2007 Gadolinium Periconceptional exposure: pregnancy and neonatal outcome. De Santis, Marco; Straface, G; Cavaliere, Anna Franca; Carducci, Brigida; Caruso, Alessandro
1-gen-2021 Gadolinium-based contrast agents hypersensitivity: A case series Nucera, Eleonora; Urbani, Sara; Buonomo, Alessandro; De Pasquale, Tiziana Maria Angela; Rizzi, Angela; Aruanno, A.; Pucci, S.
1-gen-2022 Gadoxetic acid uptake as a molecular imaging biomarker for sorafenib resistance in patients with hepatocellular carcinoma: a post hoc analysis of the SORAMIC trial Öcal, Osman; Rössler, Daniel; Gasbarrini, Antonio; Berg, Thomas; Klümpen, Heinz-Josef; Bargellini, Irene; Peynircioglu, Bora; van Delden, Otto; Schulz, Christian; Schütte, Kerstin; Iezzi, Roberto; Pech, Maciej; Malfertheiner, Peter; Sangro, Bruno; Ricke, Jens; Seidensticker, Max
1-gen-2016 Gaetano pieraccini: Public health giant who created Italian social medicine Bucci, Roberto; Colamesta, Vittoria; Sernia, Sabina; La Torre, Giuseppe
1-gen-2020 Gain and loss of abilities in type II SMA: A 12-month natural history study Coratti, Giorgia; Lucibello, Simona; Pera, Maria Carmela; Duong, T.; Muni Lofra, R.; Civitello, M.; D'Amico, Adele; Goemans, N.; Darras, B. T.; Bruno, C.; Sansone, V. A.; Day, J.; Nascimento Osorio, A.; Muntoni, F.; Montes, J.; Sframeli, M.; Finkel, R.; Mercuri, Eugenio Maria
1-gen-2024 Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study Coratti, Giorgia; Pane, Marika; Brogna, Claudia; D'Amico, A.; Pegoraro, E.; Bello, L.; Sansone, V. A.; Albamonte, E.; Ferraroli, Elisabetta; Mazzone, Elena Stacy; Fanelli, L.; Messina, S.; Sframeli, M.; Catteruccia, M.; Cicala, G.; Capasso, Anna; Ricci, M.; Frosini, S.; De Luca, G.; Rolle, E.; De Sanctis, Roberto; Forcina, N.; Norcia, G.; Passamano, L.; Scutifero, M.; Gardani, A.; Pini, A.; Monaco, G.; D'Angelo Bozzi, Michele Giovanni; Leone, D.; Zanin, Renata; Vita, G. L.; Panicucci, C.; Bruno, C.; Mongini, T.; Ricci, F.; Berardinelli, A.; Battini, Roberta; Masson, R.; Baranello, Giovanni; Dosi, C.; Bertini, Enrico Silvio; Nigro, V.; Politano, L.; Mercuri, Eugenio Maria
1-gen-2021 Gain in survival after metabolic-bariatric surgery Mingrone, Geltrude; Bornstein, Stefan R
1-gen-2022 Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome Kozycki, Christina Torres; Kodati, Shilpa; Huryn, Laryssa; Wang, Hongying; Warner, Blake M; Jani, Priyam; Hammoud, Dima; Abu-Asab, Mones S; Jittayasothorn, Yingyos; Mattapallil, Mary J; Tsai, Wanxia Li; Ullah, Ehsan; Zhou, Ping; Tian, Xiaoying; Soldatos, Ariane; Moutsopoulos, Niki; Kao-Hsieh, Marie; Heller, Theo; Cowen, Edward W; Lee, Chyi-Chia Richard; Toro, Camilo; Kalsi, Shelley; Khavandgar, Zohreh; Baer, Alan; Beach, Margaret; Long Priel, Debra; Nehrebecky, Michele; Rosenzweig, Sofia; Romeo, Tina; Deuitch, Natalie; Brenchley, Laurie; Pelayo, Eileen; Zein, Wadih; Sen, Nida; Yang, Alexander H; Farley, Gary; Sweetser, David A; Briere, Lauren; Yang, Janine; de Oliveira Poswar, Fabiano; Schwartz, Ida Vanessa D; Silva Alves, Tamires; Dusser, Perrine; Koné-Paut, Isabelle; Touitou, Isabelle; Titah, Salah Mohamed; van Hagen, Petrus Martin; van Wijck, Rogier T A; van der Spek, Peter J; Yano, Hiromi; Benneche, Andreas; Apalset, Ellen M; Jansson, Ragnhild Wivestad; Caspi, Rachel R; Kuhns, Douglas Byron; Gadina, Massimo; Takada, Hidetoshi; Ida, Hiroaki; Nishikomori, Ryuta; Verrecchia, Elena; Sangiorgi, Eugenio; Manna, Raffaele; Brooks, Brian P; Sobrin, Lucia; Hufnagel, Robert B; Beck, David; Shao, Feng; Ombrello, Amanda K; Aksentijevich, Ivona; Kastner, Daniel L
1-gen-2007 Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy Pandit, B.; Sarkozy, A.; Pennacchio, L. A.; Carta, C.; Oishi, K.; Martinelli, S.; Pogna, E. A.; Schackwitz, W.; Ustaszewska, A.; Landstrom, A.; Bos, J. M.; Ommen, S. R.; Esposito, G.; Lepri, F.; Faul, C.; Mundel, P.; Lopez Siguero, J. P.; Tenconi, Romano; Selicorni, A.; Rossi, C.; Mazzanti, L.; Torrente, I.; Marino, Bruno; Digilio, M. C.; Zampino, Giuseppe; Ackerman, M. J.; Dallapiccola, Bruno; Tartaglia, Marco; Gelb, B. T.
1-gen-2007 GAIN-OF-FUNCTION SOS1 MUTATIONS CAUSE A DISTINCTIVE FORM OF NOONAN SYNDROME. Tartaglia, Marco; Pennacchio, La; Zampino, Giuseppe; Gelb, Bd
Mostrati risultati da 11.773 a 11.792 di 31.841
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