Corpus callosum agenesis, myopathy and pinpoint pupils: consider Stormorken syndrome von Alonso‐Jiménez, A., Ramón, C., Dols‐Icardo, O., Roig, C., Gallardo, E., Clarimón, J., Núñez‐Peralta, C., Díaz‐Manera, J.

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20734. EL SEXO BIOLÓGICO CONDICIONA UNA MAYOR RESERVA EJECUTIVA Y CONDUCTUAL EN MUJERES CON DEMENCIA FRONTOTEMPORAL AUTOSÓMICA DOMINANTE von García Castro, J., Rubio Guerra, S., Selma González, J., Memel, M., Dols Icardo, O., Bejanin, A., Belbin, O., Fortea Ormaechea, J., Alcolea Rodríguez, D., Carmona Iragui, M., Barroeta, I., Santos Santos, M., Sánchez Saudinós, M., Sala Matavera, I., Heuer, H., Staffaroni, A., Casaletto, K., Boeve, B., Boxer, A., Rosen, H., Lleó Bisa, A., Illán Gala, I.

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20769. IDENTIFICACIÓN DE UNA MUTACIÓN PATOGÉNICA EN ARPP21 EN PACIENTES CON ESCLEROSIS LATERAL AMIOTRÓFICA von Carbayo Viejo, Á., Dols Icardo, O., Jericó Pascual, I., Blasco Martínez, O., López Pérez, M., Bernal Noguera, S., Rodríguez Santiago, B., Cusco, I., Turon Sans, J., Vesperinas Castro, A., Llansó Caldentey, L., Caballero Álvarez, M., Cabezas Torres, M., Pagoda Lorz, I., Torné, L., Illán Gala, I., Rubio Guerra, S., Álvarez Sánchez, E., Muñoz Llahuna, L., Valle Tamayo, N., Gelpi, E., Cortés Vicente, E., Rojas García, R.

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Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation von Suárez-Calvet, Marc, Dols-Icardo, Oriol, Lladó, Albert, Sánchez-Valle, Raquel, Hernández, Isabel, Amer, Guillermo, Antón-Aguirre, Sofía, Alcolea, Daniel, Fortea, Juan, Ferrer, Isidre, van der Zee, Julie, Dillen, Lubina, Van Broeckhoven, Christine, Molinuevo, José Luís, Blesa, Rafael, Clarimón, Jordi, Lleó, Alberto

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Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset von Billingsley, Kimberley J., Barbosa, Ines A., Bandrés-Ciga, Sara, Quinn, John P., Bubb, Vivien J., Deshpande, Charu, Botia, Juan A., Reynolds, Regina H., Zhang, David, Simpson, Michael A., Blauwendraat, Cornelis, Gan-Or, Ziv, Gibbs, J. Raphael, Nalls, Mike A., Singleton, Andrew, Ryten, Mina, Koks, Sulev

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Cortical microstructure in primary progressive aphasia: a multicenter study von Illán Gala, I, Montal, V, Borrego Écija, Sergi, Mandelli, M. L, Falgàs, N, Welch, A. E, Pegueroles, J, Santos Santos, M, Bejanin, A, Alcolea, D, Dols Icardo, O, Belbin, O, Sanchez Saudinos, M. B, Bargallo, N, Gonzalez Ortiz, S, Llado, A, Blesa, R, Dickerson, B. C, Rosen, H. J, Miller, B. L, Lleo, A, Gorno Tempini, M. L, Sanchez Valle, R, Fortea, J

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Comparison of 2 Diagnostic Criteria for the Behavioral Variant of Frontotemporal Dementia von Costa, Sónia, Suárez-Calvet, Marc, Antón, Sofia, Dols-Icardo, Oriol, Clarimón, Jordi, Alcolea, Daniel, Fortea, Juan, Carmona, María, Sala, Isabel, Sánchez-Saudinós, M. Belén, Blesa, Rafael, Lleó, Alberto

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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration von Van der Zee, J, Van Langenhove, T, Kovacs, GG, Dillen, L, Deschamps, W, Engelborghs, S, Matej, R, Vandenbulcke, M, Sieben, A, Dermaut, B, Smets, K, Van Damme, P, Merlin, C, Laureys, A, Van Den Broeck, M, Mattheijssens, M, Peeters, K, Benussi, L, Binetti, G, Ghidoni, R, Borroni, B, Padovani, A, Archetti, S, Pastor, P, Razquin, C, Ortega-Cubero, S, Hernandez, I, Boada, M, Ruiz, A, De Mendonca, A, Miltenberger-Miltenyi, G, Do Couto, FS, Sorbi, S, Nacmias, B, Bagnoli, S, Graff, C, Chiang, H-H, Thonberg, H, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Frisoni, GB, Bonvicini, C, Synofzik, M, Maetzler, W, Vom Hagen, JM, Schoels, L, Haack, TB, Strom, TM, Prokisch, H, Dols-Icardo, O, Clarimon, J, Lleo, A, Santana, I, Almeida, MR, Santiago, B, Heneka, MT, Jessen, F, Ramirez, A, Sanchez-Valle, R, Llado, A, Gelpi, E, Sarafov, S, Tournev, I, Jordanova, A, Parobkova, E, Fabrizi, GM, Testi, S, Salmon, E, Stroebel, T, Santens, P, Robberecht, W, De Jonghe, P, Martin, J-J, Cras, P, Vandenberghe, R, De Deyn, PP, Cruts, M, Sleegers, K, Van Broeckhoven, C

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Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALS von Chatterjee, M, Özdemir, S, Fritz, C, Möbius, W, Kleineidam, L, Mandelkow, E, Biernat, J, Doğdu, C, Peters, O, Cosma, N.C, Wang, X, Schneider, L.-S, Priller, J, Spruth, E, Kühn, A.A, Krause, P, Klockgether, T, Vogt, I.R, Kimmich, O, Spottke, A, Hoffmann, D.C, Fliessbach, K, Miklitz, C, McCormick, C, Weydt, P, Falkenburger, B, Brandt, M, Guenther, R, Dinter, E, Wiltfang, J, Hansen, N, Bähr, M, Zerr, I, Flöel, A, Nestor, P.J, Düzel, E, Glanz, W, Incesoy, E, Bürger, K, Janowitz, D, Perneczky, R, Rauchmann, B.S, Hopfner, F, Wagemann, O, Levin, J, Teipel, S, Kilimann, I, Goerss, D, Prudlo, J, Gasser, T, Brockmann, K, Mengel, D, Zimmermann, M, Synofzik, M, Wilke, C, Selma-González, J, Turon-Sans, J, Santos-Santos, M.A, Alcolea, D, Rubio-Guerra, S, Fortea, J, Carbayo, Á, Lleó, A, Rojas-García, R, Illán-Gala, I, Wagner, M, Frommann, I, Roeske, S, Bertram, L, Heneka, M.T, Brosseron, F, Ramirez, A, Schmid, M, Beschorner, R, Halle, A, Herms, J, Neumann, M, Barthélemy, N.R, Bateman, R.J, Rizzu, P, Heutink, P, Dols-Icardo, O, Höglinger, G, Hermann, A, Schneider, A

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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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C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts von Costa, B, Manzoni, C, Bernal-Quiros, M, Kia, D, Aguilar, M, Alvarez, I, Alvarez, V, Andreassen, O, Anfoss, M, Bagnoli, S, Benussi, L, Bernardi, L, Binetti, G, Blackburn, D, Boada, M, Borroni, B, Bowns, L, Bråthen, G, Bruni, A, Chiang, H-H, Clarimon, J, Colville, S, Conidi, M, Cope, T, Cruchaga, C, Cupidi, C, Di Battista, ME, Diehl-Schmid, J, Diez-Fairen, M, Dols-Icardo, O, Durante, E, Flisar, D, Frangipane, F, Galimberti, D, Gallo, M, Gallucc, M, Ghidoni, R, Graff, C, Grafman, J, Grossman, M, Hardy, J

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Investigation of Autosomal Genetic Sex Differences in Parkinson's disease von Makarious, MB, Bandres-Ciga, S, Grenn, FP, Tan, M, Kim, JJ, Gibbs, JR, Pihlstrøm, L, Toft, M, van Hilten, JJ, Siitonen, A, Majamaa, K, Tienari, PJ, Corvol, J-C, Wood, N, Noyce, AJ, Middlehurst, B, Kia, DA, Houlden, H, Storm, CS, Trabzuni, D, Manzoni, C, Rizig, M, Ryten, M, Escott-Price, V, Foltynie, T, Williams, N, Morrison, KE, Clarke, C, Jacobs, BM, Danjou, F, Simón-Sánchez, J, Rizzu, P, Schneider, SA, Cookson, MR, Craig, DW, Leonard, HL, Lubbe, S, Troycoco, T, Reed, X, Ross, OA, Moore, A, Alcalay, RN, Wszolek, ZK, Mufti, K, Adarmes-Gómez, AD, Alvarez, I, Alvarez, V, Barrero, FJ, Bernal-Bernal, I, Bonilla-Toribio, M, Botía, JA, Boungiorno, MT, Buiza-Rueda, D, Carrillo, F, Carrión-Claro, M, Clarimón, J, Compta, Y, Diez-Fairen, M, Dols-Icardo, O, Duarte, J, Duran, R, Ezquerra, M, Garcia, C, García-Ruiz, P, Gómez-Garre, P, Pagola, AG, Infante, J, Jesús, S, Jimenez-Escrig, A, Labrador-Espinosa, MA, Lopez-Sendon, JL, de Munain Arregui, AL, Martínez-Castrillo, JC, Méndez-Del-Barrio, C, González, MM, Mínguez, A, Mir, P, Rezola, EM, Muñoz, E, Pagonabarraga, J, Periñán-Tocino, T, Ruz, C, Rodriguez, AS, Sierra, M, Suarez-Sanmartin, E, Tabernero, C, Tejera-Parrado, C, Valldeoriola, F, Vela, L, Vives, F, Zimprich, A, Pihlstrom, L, Hassin-Baer, S, Tienari, P, Ojo, OO, Zharkinbekova, N, Akhmetzhanov, V, Kaishybayeva, G, Karimova, A, Khaibullin, T

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Identification of sixteen novel candidate genes for late onset Parkinson’s disease von Gialluisi, A, Reccia, MG, Lombardi, A, Di Giovannantonio, LG, Pietracupa, S, Ruggiero, D, Gambardella, S, Tan, M, Houlden, H, Hardy, J, Trabzuni, D, Mok, KY, Billingsley, K, Wood, NW, Lewis, P, R’Bibo, L, Manzoni, C, Foltynie, T, Williams, N, Morrison, KE, Danjou, F, Corvol, J-C, Heutink, P, Rizzu, P, Sharma, M, Gasser, T, Bandres-Ciga, S, Blauwendraat, C, Craig, DW, Narendra, D, Faghri, F, Shulman, JM, Iwaki, H, Leonard, HL, Nalls, MA, Lubbe, S, Finkbeiner, S, Mencacci, NE, Lungu, C, Singleton, AB, Alcalay, RN, Krohn, L, van Hilten, JJ, Aguilar, M, Alvarez, I, Alvarez, V, Barrero, FJ, Yarza, JAB, Blazquez, M, Bonilla-Toribio, M, Cerdan, D, Clarimón, J, Dols-Icardo, O, Duran, R, Escamilla-Sevilla, F, Fernández, M, Fernández-Santiago, R, Garcia, C, Gómez-Garre, P, Heredia, MJG, Gonzalez-Aramburu, I, Hoenicka, J, Jimenez-Escrig, A, Kulisevsky, J, Labrador-Espinosa, MA, de Munain Arregui, AL, Macias, D, Torres, IM, Marín, J, Marti, MJ, Méndez-del-Barrio, C, Mata, M, Mínguez, A, Mir, P, Pagonabarraga, J, Pastor, P, Errazquin, FP, Periñán-Tocino, T, Ruiz-Martínez, J, Sierra, M, Tabernero, C, Tartari, JP, Tolosa, E, Valldeoriola, F, Vargas-González, L, Vela, L, Vives, F, Zimprich, A, Pihlstrom, L, Koks, S, Taba, P, Hassin-Baer, S, Siitonen, A, Zharkynbekova, N, Akhmetzhanov, V, Sadykova, D, Acampora, D, D’Esposito, M, Simeone, A, Ciullo, M

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Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease von Rosas, I, Martínez, C, Clarimón, J, Lleó, A, Illán-Gala, I, Dols-Icardo, O, Borroni, B, Almeida, MR, van der Zee, J, Van Broeckhoven, C, Bruni, AC, Anfossi, M, Bernardi, L, Maletta, R, Serpente, M, Galimberti, D, Scarpini, E, Rossi, G, Caroppo, P, Benussi, L, Ghidoni, R, Binetti, G, Nacmias, B, Sorbi, S, Piaceri, I, Bagnoli, S, Antonell, A, Sánchez-Valle, R, De la Casa-Fages, B, Grandas, F, Diez-Fairen, M, Pastor, P, Ferrari, R, Álvarez, V, Menéndez-González, M

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Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets von Zhang, D, Manzoni, C, Hubbard, L, Ryten, M, Ferrari, R, Lewis, PA, Williams, N, Trabzuni, D, Hardy, J, Noyce, AJ, Kaiyrzhanov, R, Middlehurst, B, Tan, M, Houlden, H, Holmans, P, Bras, J, PhD, JQ, Mok, KY, Kinghorn, KJ, Lewis, P, Lovering, R, Escott-Price, V, Foltynie, T, Brice, A, Danjou, F, Lesage, S, Corvol, J-C, Schulte, C, Brockmann, K, Simón-Sánchez, J, Heutink, P, Rizzu, P, Sharma, M, Nicolas, A, Cookson, MR, Craig, DW, Faghri, F, Gibbs, JR, Hernandez, DG, Van Keuren-Jensen, K, Shulman, JM, Robak, L, Finkbeiner, S, Mencacci, NE, Lungu, C, Singleton, AB, Scholz, SW, Alcalay, RN, van Hilten, JJ, Marinus, J, Adarmes-Gómez, AD, Alvarez, I, Javier Barrero, F, Bergareche Yarza, JA, Bonilla-Toribio, M, Botía, JA, Boungiorno, MT, Buiza-Rueda, D, Carrillo, F, Carrión-Claro, M, Cerdan, D, Diez-Fairen, M, Ezquerra, M, Feliz, C, Fernàndez, M, Fernàndez-Santiago, R, Garcia, C, García-Ruiz, P, Gomez Heredia, MJ, Pagola, AG, Infante, J, Jimenez-Escrig, A, Kulisevsky, J, Macias, D, Torres, IM, Marín, J, Martínez-Castrillo, JC, Mèndez-del-Barrio, C, Adolfo Mínguez, MM, Mir, P, Pagonabarraga, J, Pastor, P, Errazquin, FP, Ruiz-Martínez, J, Ruz, C, Rodriguez, AS, Suarez-Sanmartin, E, Tabernero, C, Tartari, JP, Tejera-Parrado, C, Valldeoriola, F, Vargas-González, L, Vela, L, Vives, F, Pihlstrom, L, Toft, M, Hassin-Baer, S, Smith, C, Guelfi, MS, D'sa, K

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of lon... von van der Lee, SJ, Conway, OJ, Jansen, I, Carrasquillo, MM, van den Akker, E, Hernández, I, van Eijk, KR, Chen, JA, Zettergren, A, Andlauer, TFM, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, JE, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, MJ, Blennow, K, Skoog, I, Friese, MA, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, CM, Indakoetxea, B, Collij, LE, Scherer, M, Morenas-Rodríguez, E, Ironside, JW, van Berckel, BNM, Alcolea, D, Wiendl, H, Strickland, SL, Pastor, P, Rodríguez Rodríguez, E, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, Netherlands Brain Bank (NBB), Boeve, BF, Petersen, RC, Ferman, TJ, van Gerpen, JA, Reinders, MJT, Uitti, RJ, Tárraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, MC, Boada, M, Zettl, UK, van Schoor, NM, Beekman, M, Allen, M, Masliah, E, de Munain, AL, Pantelyat, A, Wszolek, ZK, Ross, OA, Dickson, DW, Graff-Radford, NR, Knopman, D, Rademakers, R, Lemstra, AW, Pijnenburg, YAL, Scheltens, P, Chinnery, PF, Hemmer, B, Huisman, MA, Troncoso, J, Moreno, F, Nohr, EA, Sørensen, TIA, Sánchez-Juan, P, Posthuma, D, Clarimón, J, Christensen, K, Scholz, SW, Ruiz, A, Slagboom, E, van der Flier, WM, Holstege, H

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies von Nalls, MA, Blauwendraat, C, Vallerga, CL, Heilbron, K, Bandres-Ciga, S, Chang, D, Tan, M, Kia, DA, Noyce, AJ, Xue, A, Bras, J, Young, E, von Coelln, R, Simón-Sánchez, J, Schulte, C, Sharma, M, Krohn, L, Pihlstrøm, L, Siitonen, A, Iwaki, H, Leonard, H, Faghri, F, Gibbs, JR, Hernandez, DG, Scholz, SW, Botia, JA, Martinez, M, Corvol, JC, Lesage, S, Jankovic, J, Shulman, LM, Sutherland, M, Tienari, P, Majamaa, K, Toft, M, Andreassen, OA, Bangale, T, Brice, A, Yang, J, Gan-Or, Z, Gasser, T, Heutink, P, Shulman, JM, Wood, NW, Hinds, DA, Hardy, JA, Morris, HR, Gratten, J, Visscher, PM, Graham, RR, Singleton, AB, Adarmes-Gómez, AD, Aguilar, M, Aitkulova, A, Akhmetzhanov, V, Alcalay, RN, Alvarez, I, Alvarez, V, Barrero, FJ, Bergareche Yarza, JA, Bernal-Bernal, I, Billingsley, K, Blazquez, M, Bonilla-Toribio, M, Botía, JA, Boungiorno, MT, Brockmann, K, Bubb, V, Buiza-Rueda, D, Cámara, A, Carrillo, F, Carrión-Claro, M, Cerdan, D, Chelban, V, Clarimón, J, Clarke, C, Compta, Y, Cookson, MR, Craig, DW, Danjou, F, Diez-Fairen, M, Dols-Icardo, O, Duarte, J, Duran, R, Escamilla-Sevilla, F, Escott-Price, V, Ezquerra, M, Feliz, C, Fernández, M, Fernández-Santiago, R, Finkbeiner, S, Foltynie, T, Garcia, C, García-Ruiz, P, Gomez Heredia, MJ, Gómez-Garre, P, González, MM, Gonzalez-Aramburu, I, Guelfi, S, Guerreiro, R

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity von van der Lee, SJ, Conway, OJ, Jansen, I, Carrasquillo, MM, van den Akker, E, Hernández, I, van Eijk, KR, Chen, JA, Zettergren, A, Andlauer, TFM, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, JE, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, MJ, Blennow, K, Skoog, I, Friese, MA, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, CM, Indakoetxea, B, Collij, LE, Scherer, M, Morenas-Rodríguez, E, Ironside, JW, van Berckel, BNM, Alcolea, D, Wiendl, H, Strickland, SL, Pastor, P, Rodríguez Rodríguez, E, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer, EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The Interna, IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, Netherlands Brain Bank (NBB), Boeve, BF, Petersen, RC, Ferman, TJ, van Gerpen, JA, Reinders, MJT, Uitti, RJ, Tárraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, MC, Boada, M, Zettl, UK, van Schoor, NM, Beekman, M, Allen, M, Masliah, E, de Munain, AL, Pantelyat, A, Wszolek, ZK, Ross, OA, Dickson, DW, Graff-Radford, NR, Knopman, D, Rademakers, R, Lemstra, AW, Pijnenburg, YAL, Scheltens, P, Chinnery, PF, Hemmer, B, Huisman, MA, Troncoso, J, Moreno, F, Nohr, EA, Sørensen, TIA, Sánchez-Juan, P, Posthuma, D, Clarimón, J, Christensen, K, Scholz, SW, Ruiz, A, Slagboom, E, van der Flier, WM, Holstege, H

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Cortical microstructure in primary progressive aphasia: a multicenter study von Illán-Gala, Ignacio, Montal, Victor, Borrego-Écija, Sergi, Mandelli, Maria Luisa, Falgàs, Neus, Welch, Ariane E, Pegueroles, Jordi, Santos-Santos, Miguel, Bejanin, Alexandre, Alcolea, Daniel, Dols-Icardo, Oriol, Belbin, Olivia, Sánchez-Saudinós, Mª Belén, Bargalló, Nuria, González-Ortiz, Sofía, Lladó, Albert, Blesa, Rafael, Dickerson, Bradford C, Rosen, Howard J, Miller, Bruce L, Lleó, Alberto, Gorno-Tempini, Maria Luisa, Sánchez-Valle, Raquel, Fortea, Juan

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Correction: Cortical microstructure in primary progressive aphasia: a multicenter study von Illán-Gala, Ignacio, Montal, Victor, Borrego-Écija, Sergi, Mandelli, Maria Luisa, Falgàs, Neus, Welch, Ariane E., Pegueroles, Jordi, Santos-Santos, Miguel, Bejanin, Alexandre, Alcolea, Daniel, Dols-Icardo, Oriol, Belbin, Olivia, Sánchez-Saudinós, Mª. Belén, Bargalló, Nuria, González-Ortiz, Sofía, Lladó, Albert, Blesa, Rafael, Dickerson, Bradford C., Rosen, Howard J., Miller, Bruce L., Lleó, Alberto, Gorno-Tempini, Maria Luisa, Sánchez-Valle, Raquel, Fortea, Juan

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