Sfoglia per Rivista JAMA NEUROLOGY
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease
2022 Le Guen, Yann; Belloy, Michael E; Grenier-Boley, Benjamin; de Rojas, Itziar; Castillo-Morales, Atahualpa; Jansen, Iris; Nicolas, Aude; Bellenguez, Céline; Dalmasso, Carolina; Küçükali, Fahri; Eger, Sarah J; Rasmussen, Katrine Laura; Thomassen, Jesper Qvist; Deleuze, Jean-François; He, Zihuai; Napolioni, Valerio; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick G; van Duijn, Cornelia; Tsolaki, Magda; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Rossi, Giacomina; Hiltunen, Mikko; Sims, Rebecca; van der Flier, Wiesje M; Ramirez, Alfredo; Andreassen, Ole A; Frikke-Schmidt, Ruth; Williams, Julie; Ruiz, Agustín; Lambert, Jean-Charles; Greicius, Michael D; Arosio, Beatrice; Benussi, Luisa; Boland, Anne; Borroni, Barbara; Caffarra, Paolo; Daian, Delphine; Daniele, Antonio; Debette, Stéphanie; Dufouil, Carole; Düzel, Emrah; Galimberti, Daniela; Giedraitis, Vilmantas; Grimmer, Timo; Graff, Caroline; Grünblatt, Edna; Hanon, Olivier; Hausner, Lucrezia; Heilmann-Heimbach, Stefanie; Holstege, Henne; Hort, Jakub; Jürgen, Deckert; Kuulasmaa, Teemu; van der Lugt, Aad; Masullo, Carlo; Mecocci, Patrizia; Mehrabian, Shima; de Mendonça, Alexandre; Moebus, Susanne; Nacmias, Benedetta; Nicolas, Gael; Olaso, Robert; Papenberg, Goran; Parnetti, Lucilla; Pasquier, Florence; Peters, Oliver; Pijnenburg, Yolande A L; Popp, Julius; Rainero, Innocenzo; Ramakers, Inez; Riedel-Heller, Steffi; Scarmeas, Nikolaos; Scheltens, Philip; Scherbaum, Norbert; Schneider, Anja; Seripa, Davide; Soininen, Hilkka; Solfrizzi, Vincenzo; Spalletta, Gianfranco; Squassina, Alessio; van Swieten, John; Tegos, Thomas J; Tremolizzo, Lucio; Verhey, Frans; Vyhnalek, Martin; Wiltfang, Jens; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Real, Luis M; Álvarez, Victoria; Bullido, María J; Clarimon, Jordi; García-Alberca, José María; Mir, Pablo; Moreno, Fermin; Pastor, Pau; Piñol-Ripoll, Gerard; Molina-Porcel, Laura; Pérez-Tur, Jordi; Rodríguez-Rodríguez, Eloy; Royo, Jose Luís; Sánchez-Valle, Raquel; Dichgans, Martin; Rujescu, Dan
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders.
2018 Savarese, M; Maggi, L; Vihola, A; Jonson, Ph; Tasca, G; De Ruggiero, Luigi; Bello, L; Magri, F; Giugliano, T; Torella, A; Evilä, A; Di Fruscio, G; Vanakker, O; Gibertini, S; Vercelli, L; Ruggieri, A; Antozzi, C; Luque, H; Janssens, S; Pasanisi, Mb; Fiorillo, Claudio; Raimondi, M; Ergoli, M; Politano, L; Bruno, C; Rubegni, A; Pane, Marika; Santorelli, Fm; Minetti, C; Angelini, Carlo; De Bleecker, J; Moggio, M; Mongini, T; Comi, Gp; Santoro, L; Mercuri, Eugenio Maria; Pegoraro, E; Mora, M; Hackman, P; Udd, B; Nigro, V.
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2022 | Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease | Le Guen, Yann; Belloy, Michael E; Grenier-Boley, Benjamin; de Rojas, Itziar; Castillo-Morales, Atahualpa; Jansen, Iris; Nicolas, Aude; Bellenguez, Céline; Dalmasso, Carolina; Küçükali, Fahri; Eger, Sarah J; Rasmussen, Katrine Laura; Thomassen, Jesper Qvist; Deleuze, Jean-François; He, Zihuai; Napolioni, Valerio; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick G; van Duijn, Cornelia; Tsolaki, Magda; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Rossi, Giacomina; Hiltunen, Mikko; Sims, Rebecca; van der Flier, Wiesje M; Ramirez, Alfredo; Andreassen, Ole A; Frikke-Schmidt, Ruth; Williams, Julie; Ruiz, Agustín; Lambert, Jean-Charles; Greicius, Michael D; Arosio, Beatrice; Benussi, Luisa; Boland, Anne; Borroni, Barbara; Caffarra, Paolo; Daian, Delphine; Daniele, Antonio; Debette, Stéphanie; Dufouil, Carole; Düzel, Emrah; Galimberti, Daniela; Giedraitis, Vilmantas; Grimmer, Timo; Graff, Caroline; Grünblatt, Edna; Hanon, Olivier; Hausner, Lucrezia; Heilmann-Heimbach, Stefanie; Holstege, Henne; Hort, Jakub; Jürgen, Deckert; Kuulasmaa, Teemu; van der Lugt, Aad; Masullo, Carlo; Mecocci, Patrizia; Mehrabian, Shima; de Mendonça, Alexandre; Moebus, Susanne; Nacmias, Benedetta; Nicolas, Gael; Olaso, Robert; Papenberg, Goran; Parnetti, Lucilla; Pasquier, Florence; Peters, Oliver; Pijnenburg, Yolande A L; Popp, Julius; Rainero, Innocenzo; Ramakers, Inez; Riedel-Heller, Steffi; Scarmeas, Nikolaos; Scheltens, Philip; Scherbaum, Norbert; Schneider, Anja; Seripa, Davide; Soininen, Hilkka; Solfrizzi, Vincenzo; Spalletta, Gianfranco; Squassina, Alessio; van Swieten, John; Tegos, Thomas J; Tremolizzo, Lucio; Verhey, Frans; Vyhnalek, Martin; Wiltfang, Jens; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Real, Luis M; Álvarez, Victoria; Bullido, María J; Clarimon, Jordi; García-Alberca, José María; Mir, Pablo; Moreno, Fermin; Pastor, Pau; Piñol-Ripoll, Gerard; Molina-Porcel, Laura; Pérez-Tur, Jordi; Rodríguez-Rodríguez, Eloy; Royo, Jose Luís; Sánchez-Valle, Raquel; Dichgans, Martin; Rujescu, Dan | |
| 1-gen-2018 | Interpreting Genetic Variants in Titin in Patients With Muscle Disorders. | Savarese, M; Maggi, L; Vihola, A; Jonson, Ph; Tasca, G; De Ruggiero, Luigi; Bello, L; Magri, F; Giugliano, T; Torella, A; Evilä, A; Di Fruscio, G; Vanakker, O; Gibertini, S; Vercelli, L; Ruggieri, A; Antozzi, C; Luque, H; Janssens, S; Pasanisi, Mb; Fiorillo, Claudio; Raimondi, M; Ergoli, M; Politano, L; Bruno, C; Rubegni, A; Pane, Marika; Santorelli, Fm; Minetti, C; Angelini, Carlo; De Bleecker, J; Moggio, M; Mongini, T; Comi, Gp; Santoro, L; Mercuri, Eugenio Maria; Pegoraro, E; Mora, M; Hackman, P; Udd, B; Nigro, V. |
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