Sfoglia per ???browse.type.metadata.subjectErc2011???  LS2_9 - Genetic epidemiology

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Data di pubblicazione Titolo Autore(i) File
1-gen-2014 A case-control study on proinflammatory genetic Polymorphisms on sudden sensorineural hearing loss Cadoni, Gabriella; Gaetani, Eleonora; Picciotti, Pasqualina Maria; Arzani, Dario; Quarta, Miriam; Giannantonio, Sara; Paludetti, Gaetano; Boccia, Stefania
1-gen-2014 A case-control study on the effect of metabolic gene polymorphisms, nutrition, and their interaction on the risk of non-alcoholic fatty liver disease Miele, L; Dall'Armi, V; Cefalo, C; Nedovic, B; Arzani, D; Amore, R; Rapaccini, G; Gasbarrini, A; Ricciardi, W; Grieco, Antonio; Boccia, S.
1-gen-2012 A case-control study on the effects of the apolipoprotein E genotypes in nonalcoholic fatty liver disease De Feo, Emma; Cefalo, Consuelo; Arzani, Dario; Amore, R; Landolfi, Raffaele; Grieco, Antonio; Ricciardi, Gualtiero; Miele, Luca; Boccia, Stefania
1-gen-2015 A functional 5HT2A receptor polymorphism (His452Tyr) and memory performances in Alzheimer's disease Guglielmi, Valeria; Bizzarro, Alessandra; Valenza, A; Lauria, Alessandra; Tiziano, Francesco Danilo; Lomastro, R; Masullo, Carlo
1-gen-2009 A premature infant with Costello syndrome due to a rare G13C HRAS mutation Piccione, Maria; Pomponi, Maria Grazia; Pietrobono, Roberta; Neri, Giovanni
1-gen-2009 A premature infant with Costello syndrome due to a rare G13C HRAS mutation. Neri, Giovanni; Piccione, M; Piro, Maddalena; Pomponi, Maria Grazia; Pietrobono, Roberta; Candela, E; Gabriele, B; Corsello, Giovanni
1-gen-2015 A Rare Truncating BRCA2 Variant and Genetic Susceptibility to Upper Aerodigestive Tract Cancer Delahaye Sourdeix, M; Anantharaman, D; Timofeeva, Mn; Gaborieau, V; Chabrier, A; Vallee, Mp; Lagiou, P; Holcatova, I; Richiardi, L; Kjaerheim, K; Agudo, A; Castellsague, X; Macfarlane, Tv; Barzan, L; Canova, C; Thakker, Ns; Conway, Di; Znaor, A; Healy, Cm; Ahrens, W; Zaridze, D; Szeszenia Dabrowska, N; Lissowska, J; Fabianova, E; Mates, In; Bencko, V; Foretova, L; Janout, V; Curado, Mp; Koifman, S; Menezes, A; Wunsch Filho, V; Eluf Neto, J; Boffetta, P; Fernandez Garrote, L; Polesel, J; Lener, M; Jaworowska, E; Lubiński, J; Boccia, Stefania; Rajkumar, T; Samant, Ta; Mahimkar, Mb; Matsuo, K; Franceschi, S; Byrnes, G; Brennan, P; Mckay, Jd
1-gen-2010 A RESTRICTED SPECTRUM OF NRAS MUTATION CAUSES NOONAN SYNDROME Zampino, Giuseppe; Digilio, C; Stuppia, L; Pantaleoni, F; Tartaglia, Marco; Dallapiccola, Bruno; Dentici, M. L; Zenker, M.
1-gen-2009 ALDH2 and Head and Neck Cancer: a Meta-analysis implementing a Mendelian Randomization approach Boccia, Stefania; Hashibe, Mia; Gallì, Paola; De Feo, Emma; Asakage, Takahiro; Hashimoto, Tomoko; Hiraki, Akio; Katoh, Takahiko; Nomura, Takeshi; Yokoyama, Akira; Van Duijn, Cornelia M; Ricciardi, Gualtiero; Boffetta, Paolo
1-gen-2012 Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism. Pola, Roberto; Gaetani, Eleonora
1-gen-2014 Association between Polymorphisms rs1333040 and rs7865618 of Chromosome 9p21 and Sporadic Brain Arteriovenous Malformations. Sturiale, Cl; Fontanella, Mm; Gatto, Ilaria; Puca, Alfredo; Giarretta, Igor; D'Arrigo, Sonia; Lofrese, Giorgio; Rainero, I; Gallone, S; Pinessi, L; Ducati, Alessandro; Maira, Giulio; Pola, Roberto
1-gen-2013 Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations Sturiale, Carmelo Lucio; Gatto, Ilaria; Puca, Alfredo; D'Arrigo, Sonia; Giarretta, Igor; Albanese, Alessio; Di Rocco, Concezio; Maira, Giulio; Pola, Roberto
1-gen-2007 Association of MBL2 variants with early preterm delivery Ameglio, F.; Romagnoli, Costantino; Vento, Giovanni; Giardina, Bruno; Capoluongo, E.
1-gen-2017 Association study reveals novel risk loci for sporadic inclusion body myositis Johari, M.; Arumilli, M.; Palmio, J.; Savarese, M.; Tasca, G.; Mirabella, M.; Sandholm, N.; Lohi, H.; Hackman, P.; Udd, B.
1-gen-2015 ATXN2 polyQ intermediate repeats are a modifier of ALS survival Chiò, A; Calvo, A; Moglia, C; Canosa, A; Brunetti, M; Barberis, M; Restagno, G; Conte, Amelia; Bisogni, Giulia; Marangi, Giuseppe; Moncada, Alice; Lattante, Serena; Zollino, Marcella; Sabatelli, Mario; Bagarotti, A; Corrado, L; Mora, G; Bersano, E; Mazzini, L; D'Alfonso, S.
1-gen-2012 Autism and intellectual disability: two sides of the same coin. Neri, Giovanni; Schwartz, Charles E.
1-gen-2011 Cardio-Facio-cutaneous syndrome: phenotypic variability and differential diagnosis in 3 cases with de novo BRAF mutations Neri, Giovanni; Mancano, Giorgia; Pomponi, Maria Grazia; Ozcelik, A; Gucuyener, K.
1-gen-2010 A case-control study on the effects of apoE genotype on head and neck cancer risk De Feo, Emma; Rowell, Jessica; Cadoni, Gabriella; Nicolotti, Nicola; Arzani, Dario; Giorgio, Arianna; Amore, Rosarita; Paludetti, Gaetano; Ricciardi, Gualtiero; Boccia, Stefania
1-gen-2021 Change in age distribution of COVID-19 deaths with the introduction of COVID-19 vaccination Pastorino, R; Pezzullo, Am; Villani, L; Causio, Fa; Axfors, C; Contopoulos-Ioannidis, Dg; Boccia, S; Ioannidis, Jpa
1-gen-2014 Characterization of the rs2802292 SNP identifies FOXO3A as a modifier locus predicting cancer risk in patients with PJS and PHTS hamartomatous polyposis syndromes. Forte, Giovanna; Grossi, Valentina; Celestini, Valentina; Lucisano, Giuseppe; Scardapane, Marco; Varvara, Dora; Patruno, Margherita; Bagnulo, Rosanna; Loconte, Daria; Giunti, Laura; Petracca, Antonio; Giglio, Sabrina; Genuardi, Maurizio; Pellegrini, Fabio; Resta, Nicoletta; Simone, Cristiano
Mostrati risultati da 1 a 20 di 139
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