Treffer 1 - 20 von 20 für Suche 'María Fox Pascual', Suchdauer: 1,50s Treffer weiter einschränken
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    Prevalence of amyloid‐β pathology in distinct variants of primary progressive aphasia von Bergeron, David, Gorno‐Tempini, Maria L., Rabinovici, Gil D., Santos‐Santos, Miguel A., Seeley, William, Miller, Bruce L., Pijnenburg, Yolande, Keulen, M. Antoinette, Groot, Colin, van Berckel, Bart N. M., van der Flier, Wiesje M., Scheltens, Philip, Rohrer, Jonathan D., Warren, Jason D., Schott, Jonathan M., Fox, Nick C., Sanchez‐Valle, Raquel, Grau‐Rivera, Oriol, Gelpi, Ellen, Seelaar, Harro, Papma, Janne M., van Swieten, John C., Hodges, John R., Leyton, Cristian E., Piguet, Olivier, Rogalski, Emily J., Mesulam, Marsel M., Koric, Lejla, Nora, Kristensen, Pariente, Jeéreémie, Dickerson, Bradford, Mackenzie, Ian R., Hsiung, Ging‐Yuek R., Belliard, Serge, Irwin, David J., Wolk, David A., Grossman, Murray, Jones, Matthew, Harris, Jennifer, Mann, David, Snowden, Julie S., Chrem‐Mendez, Patricio, Calandri, Ismael L., Amengual, Alejandra A., Miguet‐Alfonsi, Carole, Magnin, Eloi, Magnani, Giuseppe, Santangelo, Roberto, Deramecourt, Vincent, Pasquier, Florence, Mattsson, Niklas, Nilsson, Christer, Hansson, Oskar, Keith, Julia, Masellis, Mario, Black, Sandra E., Matías‐Guiu, Jordi A., Cabrera‐Martin, María‐Nieves, Paquet, Claire, Dumurgier, Julien, Teichmann, Marc, Sarazin, Marie, Bottlaender, Michel, Dubois, Bruno, Rowe, Christopher C., Villemagne, Victor L., Vandenberghe, Rik, Granadillo, Elias, Teng, Edmond, Mendez, Mario, Meyer, Philipp T., Frings, Lars, Lleó, Alberto, Blesa, Rafael, Fortea, Juan, Seo, Sang Won, Diehl‐Schmid, Janine, Grimmer, Timo, Frederiksen, Kristian Steen, Sánchez‐Juan, Pascual, Chételat, Gaël, Jansen, Willemijn, Bouchard, Rémi W., Laforce, Robert Jr, Visser, Pieter Jelle, Ossenkoppele, Rik

    Veröffentlicht in Annals of neurology

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    Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen G. J., Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J., Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, DeStefano, Anita L., Farrer, Lindsay A., Fox, Nick C., Galimberti, Daniela, Gille, Johan J. P., Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Marc, Lemstra, Afina W., Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M., Marshall, Rachel, Martin, Eden R., Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O., Morgan, Kevin, Myers, Richard M., Nacmias, Benedetta, Naj, Adam C., Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T., Riedel-Heller, Steffi G., Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S., Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D., Scheltens, Philip, Schott, Jonathan M., Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A., Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André G., van der Lee, Sven J., Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C., Greicius, Michael D., Yokoyama, Jennifer S., Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M., van Duijn, Cornelia M., Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

    Veröffentlicht in Nature genetics

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    Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary, Berr, Claudine, Bis, Joshua, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, Destefano, Anita, Farrer, Lindsay, Fernández, Maria Victoria, Fox, Nick, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan, Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris, Kraaij, Robert, Lathrop, Marc, Lemstra, Afina, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel, Marshall, Rachel, Martin, Eden, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel, Morgan, Kevin, Myers, Richard, Nacmias, Benedetta, Naj, Adam, Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret, Raybould, Rachel, Redon, Richard, Reinders, Marcel, Richard, Anne-Claire, Riedel-Heller, Steffi, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard, Scheltens, Philip, Schott, Jonathan, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André, van der Lee, Sven, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John, Greicius, Michael, Yokoyama, Jennifer, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo

    Veröffentlicht in Nature genetics

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    Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia von Bergeron, David, Gorno-Tempini, Maria L, Rabinovici, Gil D, Santos-Santos, Miguel A, Seeley, William, Miller, Bruce L, Pijnenburg, Yolande, Keulen, M. Antoinette, Groot, Colin, van Berckel, Bart N.M, van der Flier, Wiesje M, Scheltens, Philip, Rohrer, Jonathan D, Warren, Jason D, Schott, Jonathan M, Fox, Nick C, Sanchez-Valle, Raquel, Grau-Rivera, Oriol, Gelpi, Ellen, Seelaar, Harro, Papma, Janne M, van Swieten, John C, Hodges, John R, Leyton, Cristian E, Piguet, Olivier, Rogalski, Emily J, Mesulam, Marsel M, Koric, Lejla, Nora, Kristensen, Pariente, Jeereemie, Dickerson, Bradford, Mackenzie, Ian R, Hsiung, Ging-Yuek R, Belliard, Serge, Irwin, David J, Wolk, David A, Grossman, Murray, Jones, Matthew, Harris, Jennifer, Mann, David, Snowden, Julie S, Chrem-Mendez, Patricio, Calandri, Ismael L, Amengual, Alejandra A, Miguet-Alfonsi, Carole, Magnin, Eloi, Magnani, Giuseppe, Santangelo, Roberto, Deramecourt, Vincent, Pasquier, Florence, Mattsson, Niklas, Nilsson, Christer, Hansson, Oskar, Keith, Julia, Masellis, Mario, Black, Sandra E, Matias-Guiu, Jordi A, Cabrera-Martin, Maria-Nieves, Paquet, Claire, Dumurgier, Julien, Teichmann, Marc, Sarazin, Marie, Bottlaender, Michel, Dubois, Bruno, Rowe, Christopher C, Villemagne, Victor L, Vandenberghe, Rik, Granadillo, Elias, Teng, Edmond, Mendez, Mario, Meyer, Philipp T, Frings, Lars, Lleo, Alberto, Blesa, Rafael, Fortea, Juan, Seo, Sang Won, Diehl-Schmid, Janine, Grimmer, Timo, Frederiksen, Kristian Steen, Sanchez-Juan, Pascual, Chetelat, Gael, Jansen, Willemijn, Bouchard, Remi W, Laforce, Robert, Visser, Pieter Jelle, Ossenkoppele, Rik

    Veröffentlicht in ANNALS OF NEUROLOGY

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    Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen GJ, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan JP, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M Arfan, Ikram, M Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel MAM, Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O, Morgan, Kevin, Myers, Richard M, Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel JT, Richard, Anne-Claire, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D, Scheltens, Philip, Schott, Jonathan M, Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

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    Summary statistics for "Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's Disease" von Henne Holstege, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, Van Rooij, Jeroen G.J., Sims, Rebecca, Ahmad, Shahzad, Norsworthy, Penny J., Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Alzheimer's Disease Neuroimaging Initiative (ADNI) Database, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, J. Nicholas Cochran, Daniele, Antonio, Jean-François Dartigues, Debette, Stéphanie, Jean-François Deleuze, Denning, Nicola, Fernandez, Maria Victoria, Fox, Nick C., Galimberti, Daniela, Gille, Hans, Guen, Yann Le, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, M. Arfan Ikram, M. Kamran Ikram, Jansen, Iris, Kraaij, Robert, Lathrop, Marc, Afina W. Lemstra, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M., Marshall, Rachel, Martin, Eden R, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O., Myers, Richard M., Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pau Pastor, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J.T., Anne-Claire Richard, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S., Sanchez-Juan, Pascual, Schellenberg, Gerard D., Scheltens, Philip, Schott, Jonathan M., Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik, Sorbi, Sandro, Van Spaendonk, Resie, Spalletta, Gianfranco, Niccólo Tesi, Tijms, Betty, Uitterlinden, André G, Van Der Lee, Sven J., De Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Li-San Wang, Zarea, Aline, Van Swieten, John C., Greicius, Michael, Yokoyama, Jennifer S., Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, Van Der Flier, Wiesje M., Van Duijn, Cornelia M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Jean-Charles Lambert

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