Restructuring complex for cosmetic compositions von COPE SANDRA E

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Restructuring complex for cosmetic compositions von Cope, Sandra E

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Rapid implementation of mobile technology for real-time epidemiology of COVID-19 von Drew, David A, Nguyen, Long H, Steves, Claire J, Menni, Cristina, Freydin, Maxim, Varsavsky, Thomas, Sudre, Carole H, Cardoso, M Jorge, Ourselin, Sebastien, Wolf, Jonathan, Spector, Tim D, Chan, Andrew T

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The COronavirus Pandemic Epidemiology (COPE) Consortium: A Call to Action von Chan, Andrew T, Drew, David A, Nguyen, Long H, Joshi, Amit D, Ma, Wenjie, Guo, Chuan-Guo, Lo, Chun-Han, Mehta, Raaj S, Kwon, Sohee, Sikavi, Daniel R, Magicheva-Gupta, Marina V, Fatehi, Zahra S, Flynn, Jacqueline J, Leonardo, Brianna M, Albert, Christine M, Andreotti, Gabriella, Beane-Freeman, Laura E, Balasubramanian, Bijal A, Brownstein, John S, Bruinsma, Fiona, Cowan, Annie N, Deka, Anusila, Ernst, Michael E, Figueiredo, Jane C, Franks, Paul W, Gardner, Christopher D, Ghobrial, Irene M, Haiman, Christopher A, Hall, Janet E, Deming-Halverson, Sandra L, Kirpach, Brenda, Lacey, Jr, James V, Marchand, Loïc Le, Marinac, Catherine R, Martinez, Maria Elena, Milne, Roger L, Murray, Anne M, Nash, Denis, Palmer, Julie R, Patel, Alpa V, Rosenberg, Lynn, Sandler, Dale P, Sharma, Shreela V, Schurman, Shepherd H, Wilkens, Lynne R, Chavarro, Jorge E, Eliassen, A Heather, Hart, Jaime E, Kang, Jae Hee, Koenen, Karestan C, Kubzansky, Laura D, Mucci, Lorelei A, Ourselin, Sebastien, Rich-Edwards, Janet W, Song, Mingyang, Stampfer, Meir J, Steves, Claire J, Willett, Walter C, Wolf, Jonathan, Spector, Tim

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Comparing the DNA hypermethylome with gene mutations in human colorectal cancer von Schuebel, Kornel E, Chen, Wei, Cope, Leslie, Glöckner, Sabine C, Suzuki, Hiromu, Yi, Joo-Mi, Chan, Timothy A, Van Neste, Leander, Van Criekinge, Wim, van den Bosch, Sandra, van Engeland, Manon, Ting, Angela H, Jair, Kamwing, Yu, Wayne, Toyota, Minoru, Imai, Kohzoh, Ahuja, Nita, Herman, James G, Baylin, Stephen B

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Looking Upstream: Promoting Health Equity in Philadelphia through Novel Partnership Strategies von Cope, Adrea E, Nash, David B, Brooks, Sandra E, Platt, David

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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease von Splinter, Kimberly, Adams, David R, Bacino, Carlos A, Bellen, Hugo J, Bernstein, Jonathan A, Cheatle-Jarvela, Alys M, Eng, Christine M, Esteves, Cecilia, Gahl, William A, Hamid, Rizwan, Jacob, Howard J, Kikani, Bijal, Koeller, David M, Kohane, Isaac S, Lee, Brendan H, Loscalzo, Joseph, Luo, Xi, McCray, Alexa T, Metz, Thomas O, Mulvihill, John J, Nelson, Stanley F, Palmer, Christina G.S, Phillips, John A, Pick, Leslie, Postlethwait, John H, Reuter, Chloe, Shashi, Vandana, Sweetser, David A, Tifft, Cynthia J, Walley, Nicole M, Wangler, Michael F, Westerfield, Monte, Wheeler, Matthew T, Wise, Anastasia L, Worthey, Elizabeth A, Yamamoto, Shinya, Ashley, Euan A

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Temporal order of clinical and biomarker changes in familial frontotemporal dementia von Staffaroni, Adam M., Quintana, Melanie, Wendelberger, Barbara, Heuer, Hilary W., Russell, Lucy L., Cobigo, Yann, Wolf, Amy, Petrucelli, Leonard, Gendron, Tania F., Heller, Carolin, Clark, Annie L., Taylor, Jack Carson, Wise, Amy, Ong, Elise, Forsberg, Leah, Brushaber, Danielle, Rojas, Julio C., VandeVrede, Lawren, Ljubenkov, Peter, Kramer, Joel, Casaletto, Kaitlin B., Appleby, Brian, Botha, Hugo, Dickerson, Bradford C., Domoto-Reilly, Kimiko, Fields, Julie A., Foroud, Tatiana, Gavrilova, Ralitza, Geschwind, Daniel, Ghoshal, Nupur, Goldman, Jill, Graff-Radford, Jonathon, Graff-Radford, Neill, Grossman, Murray, Hall, Matthew G. H., Hsiung, Ging-Yuek, Huey, Edward D., Irwin, David, Jones, David T., Kantarci, Kejal, Kaufer, Daniel, Knopman, David, Kremers, Walter, Lago, Argentina Lario, Lapid, Maria I., Litvan, Irene, Lucente, Diane, Mackenzie, Ian R., Mendez, Mario F., Mester, Carly, Miller, Bruce L., Onyike, Chiadi U., Rademakers, Rosa, Ramanan, Vijay K., Ramos, Eliana Marisa, Rao, Meghana, Rascovsky, Katya, Rankin, Katherine P., Roberson, Erik D., Savica, Rodolfo, Tartaglia, M. Carmela, Weintraub, Sandra, Wong, Bonnie, Cash, David M., Bouzigues, Arabella, Swift, Imogen J., Peakman, Georgia, Bocchetta, Martina, Todd, Emily G., Convery, Rhian S., Rowe, James B., Borroni, Barbara, Tiraboschi, Pietro, Masellis, Mario, Finger, Elizabeth, van Swieten, John C., Seelaar, Harro, Jiskoot, Lize C., Sorbi, Sandro, Butler, Chris R., Graff, Caroline, Gerhard, Alexander, Langheinrich, Tobias, Laforce, Robert, Sanchez-Valle, Raquel, de Mendonça, Alexandre, Moreno, Fermin, Synofzik, Matthis, Vandenberghe, Rik, Ducharme, Simon, Levin, Johannes, Danek, Adrian, Otto, Markus, Pasquier, Florence, Santana, Isabel, Kornak, John, Boeve, Bradley F., Rosen, Howard J., Rohrer, Jonathan D., Boxer, Adam. L.

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Transactional sex, HIV and health among young cisgender men and transgender women who have sex with men in Thailand von Weir, Brian W., Dun, Chen, Wirtz, Andrea L., Mon, Sandra Hsu Hnin, Qaragholi, Noor, Chemnasiri, Tareerat, Pattanasin, Sarika, Sukwicha, Wichuda, Varangrat, Anchalee, Dunne, Eileen F., Holtz, Timothy H., Janyam, Surang, Jin, Harry, Linjongrat, Danai, Mock, Philip A., Thigpen, Michael C., Rooney, James F., Sullivan, Patrick S., Hickey, Andrew C., Sirivongrangson, Pachara, Beyrer, Chris

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IRF2BPL Is Associated with Neurological Phenotypes von Marcogliese, Paul C., Rosenfeld, Jill A., Koenig, Mary Kay, Chen, Agnes H., Dickson, Patricia I., Vera, Moin U., Salamon, Noriko, Infante, Elena, Poppe, Bruce, Chung, Hyung-Lok, Zuo, Zhongyuan, Kanca, Oguz, Xia, Fan, Smith, Edward C., Jasien, Joan, Kansagra, Sujay, Lark, Robert, Riley, Kacie, Golden-Grant, Katie, Poppe, Bruce, Terryn, Wim, Adams, David R., Allard, Patrick, Bacino, Carlos A., Bick, David P., Bostwick, Bret L., Brush, Matthew, Burrage, Lindsay C., Clark, Gary D., Cooper, Cynthia M., D’Souza, Precilla, Davids, Mariska, Dell’Angelica, Esteban C., Dhar, Shweta U., Dillon, Ani, Dorrani, Naghmeh, Dorset, Daniel C., Esteves, Cecilia, Fogel, Brent L., Gahl, William A., Gourdine, Jean-Philippe F., Haendel, Melissa, Hamid, Rizwan, Hanchard, Neil A., Howerton, Ellen M., Jiang, Yong-hui, Johnston, Jean M., Krier, Joel B., Lalani, Seema R., Lau, C. Christopher, Lee, Brendan H., Levy, Shawn E., Lewis, Richard A., Lipson, Allen, Loo, Sandra K., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Martínez-Agosto, Julian A., McConkie-Rosell, Allyn, McCormack, Colleen E., Morimoto, Marie, Mulvihill, John J., Muzny, Donna M., Nelson, Stan F., Newberry, J. Scott, Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Phillips, John A., Posey, Jennifer E., Postlethwait, John H., Potocki, Lorraine, Robertson, Amy K., Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Smith, Kevin S., Splinter, Kimberly, Stoler, Joan M., Sweetser, David A., Toro, Camilo, Urv, Tiina K., Vilain, Eric, Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Walsh, Chris A., Waters, Katrina M., Westerfield, Monte, Yu, Guoyun, Zheng, Allison, Yamamoto, Shinya, Wangler, Michael F., Lee, Brendan, Nelson, Stanley F., Goldstein, David B., Bellen, Hugo J.

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Differential early subcortical involvement in genetic FTD within the GENFI cohort von Bocchetta, Martina, Todd, Emily G., Cash, David M., Convery, Rhian S., van Swieten, John C., Seelaar, Harro, Sanchez-Valle, Raquel, Moreno, Fermin, Graff, Caroline, Masellis, Mario, Carmela Tartaglia, Maria, Rowe, James B., Finger, Elizabeth, de Mendonça, Alexandre, Santana, Isabel, Butler, Chris R., Ducharme, Simon, Gerhard, Alexander, Danek, Adrian, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Le Ber, Isabelle, Rohrer, Jonathan D., Andersson, Christin, Archetti, Silvana, Arighi, Andrea, Balasa, Mircea, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Bertrand, Anne, Borrego-Ecija, Sergi, Brice, Alexis, Camuzat, Agnès, Cañada, Marta, Cantoni, Valentina, Caroppo, Paola, de Arriba, María, Di Fede, Giuseppe, Díez, Alina, Duro, Diana, Ferreira, Catarina B., Fox, Nick, Freedman, Morris, Fumagalli, Giorgio, Funkiewiez, Aurélie, Gabilondo, Alazne, Gasparotti, Roberto, Gauthier, Serge, Gazzina, Stefano, Guerreiro, Rita, Heller, Carolin, Jelic, Vesna, Keren, Ron, Kuchcinski, Gregory, Langheinrich, Tobias, Lebouvier, Thibaud, João Leitão, Maria, Lladó, Albert, Maruta, Carolina, Mitchell, Sara, Moore, Katrina, Nacmias, Benedetta, Nelson, Annabel, Nicholas, Jennifer, Öijerstedt, Linn, Olives, Jaume, Panman, Jessica, Pijnenburg, Yolande, Polito, Cristina, Premi, Enrico, Prix, Catharina, Rademakers, Rosa, Redaelli, Veronica, Rinaldi, Daisy, Rogaeva, Ekaterina, Rollin, Adeline, Rosa-Neto, Pedro, Rossi, Giacomina, Rossor, Martin, Santiago, Beatriz, Scarpini, Elio, Schönecker, Sonja, Semler, Elisa, Swift, Imogen, Tábuas-Pereira, Miguel, Tainta, Mikel, Taipa, Ricardo, Tang-Wai, David, Timberlake, Carolyn, Tiraboschi, Pietro, Veldsman, Michele, Verdelho, Ana, Warren, Jason, Wilke, Carlo, Woollacott, Ione, Wlasich, Elisabeth, Zetterberg, Henrik, Zulaica, Miren

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Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study von Pengo, Marta, Mattioli, Irene, Cantoni, Valentina, Dukart, Juergen, Gasparotti, Roberto, Buratti, Emanuele, Todd, Emily G., Bouzigues, Arabella, Cash, David M., Russell, Lucy L., Foster, Phoebe, van Swieten, John C., Jiskoot, Lize C., Galimberti, Daniela, Laforce, Robert, Moreno, Fermin, Synofzik, Matthis, Graff, Caroline, Rowe, James B., Finger, Elizabeth, de Mendonça, Alexandre, Santana, Isabel, Butler, Chris R., Ducharme, Simon, Gerhard, Alexander, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Le Ber, Isabelle, Rohrer, Jonathan D., Heller, Carolin, Samra, Kiran, Shafei, Rachelle, Timberlake, Carolyn, Arighi, Andrea, Rossi, Giacomina, Giaccone, Giorgio, Caroppo, Paola, Tiraboschi, Pietro, Prioni, Sara, Redaelli, Veronica, Tang-Wai, David, Rogaeva, Ekaterina, Bartha, Robart, Poos, Jackie, van Minkelen, Rick, Nacmias, Benedetta, Polito, Cristina, Veldsman, Michele, Andersson, Christin, Öijerstedt, Linn, Jelic, Vesna, Thompson, Paul, Langheinrich, Tobias, Lladó, Albert, Antonell, Anna, Olives, Jaume, Balasa, Mircea, Bargalló, Nuria, Verdelho, Ana, Maruta, Carolina, Ferreira, Catarina B., Miltenberger, Gabriel, Gabilondo, Alazne, Gorostidi, Ana, Villanua, Jorge, Cañada, Marta, Tainta, Mikel, Zulaica, Miren, Barandiaran, Myriam, Alves, Patricia, Bender, Benjamin, Wilke, Carlo, Vogels, Annick, Vandenbulcke, Mathieu, Van Damme, Philip, Bruffaerts, Rose, Poesen, Koen, Rosa-Neto, Pedro, Gauthier, Serge, Camuzat, Agnès, Bertrand, Anne, Rinaldi, Daisy, Colliot, Olivier, Prix, Catharina, Wlasich, Elisabeth, Wagemann, Olivia, Loosli, Sandra, Schönecker, Sonja, Lombardi, Jolina, Rollin, Adeline, Kuchcinski, Gregory, Bertoux, Maxime, Deramecourt, Vincent, Santiago, Beatriz, Duro, Diana, Leitão, Maria João, Almeida, Maria Rosario, Tábuas-Pereira, Miguel, Afonso, Sónia

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Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay von Sullivan, Jennifer A., Shashi, Vandana, Jiang, Yong-hui, Stong, Nicholas, Fiala, Elise, Willing, Marcia, Pfundt, Rolph, Kleefstra, Tjitske, Orellana, Carmen, Monfort, Sandra, Roscioli, Tony, Jones, Wendy D., Sebastian, Jessica, Sonal, Desai, Sakkubai, Naidu, Faivre, Laurence, Krantz, Ian D., Adams, David R., Alejandro, Mercedes E., Azamian, Mahshid S., Barseghyan, Hayk, Batzli, Gabriel F., Beggs, Alan H., Bican, Anna, Birch, Camille L., Bonner, Devon, Boone, Braden E., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Chen, Shan, Coakley, Terra R., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dillon, Ani, Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Dorset, Daniel C., Eskin, Ascia, Friedman, Noah D., Glanton, Emily, Godfrey, Rena A., Gould, Sarah E., Gropman, Andrea L., Hom, Jason, Jacob, Howard J., Jain, Mahim, Jiang, Yong-hui, Kohane, Isaac S., Krieg, Elizabeth L., Lau, C. Christopher, Lazar, Jozef, Lee, Brendan H., Lee, Hane, Lewis, Richard A., Loo, Sandra K., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martínez-Agosto, Julian A., Marwaha, Shruti, May, Thomas, McCray, Alexa T., Might, Matthew, Mulvihill, John J., Murphy, Jennifer L., Nelson, Stan F., Newman, John H., Novacic, Donna, Orange, Jordan S., Pallais, J. Carl, Pena, Loren D.M., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Rosenfeld, Jill A., Sharma, Prashant, Shashi, Vandana, Signer, Rebecca, Sinsheimer, Janet S., Spillmann, Rebecca C., Splinter, Kimberly, Stoler, Joan M., Stong, Nicholas, Sweetser, David A., Tran, Alyssa A., Valivullah, Zaheer M., Wahl, Colleen E., Waters, Katrina M., Westerfield, Monte, Wise, Anastasia L., Worthey, Elizabeth A., Yang, Yaping, Zastrow, Diane B., Campeau, Philippe M.

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Neuronal pentraxin 2: a synapse-derived CSF biomarker in genetic frontotemporal dementia von van der Ende, EL, Xiao, MF, Xu, DS, Poos, JM, Panman, JL, Jiskoot, LC, Meeter, LH, Dopper, EGP, Papma, JM, Heller, C, Convery, R, Moore, K, Bocchetta, M, Neason, M, Peakman, G, Cash, DM, Teunissen, CE, Graff, C, Synofzik, M, Moreno, F, Finger, E, Sanchez-Valle, R, Vandenberghe, R, Laforce, R, Masellis, M, Tartaglia, MC, Rowe, JB, Butler, CR, Ducharme, S, Gerhard, A, Danek, A, Levin, J, Pijnenburg, YAL, Otto, M, Borroni, B, Tagliavini, F, de Mendonca, A, Santana, I, Galimberti, D, Seelaar, H, Rohrer, JD, Worley, PF, van Swieten, JC

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A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative von Schoch, Kelly, Spillmann, Rebecca, Tan, Queenie K.-G., McConkie-Rosell, Allyn, Jiang, Yong-Hui, Goldstein, David B., Adams, David R., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Beggs, Alan H., Birch, Camille L., Bonner, Devon, Boone, Braden E., Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Davidson, Jean M., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Friedman, Noah D., Gahl, William A., Goldstein, David B., Gourdine, Jean-Philippe F., Haendel, Melissa, Handley, Lori H., Krasnewich, Donna M., Krier, Joel B., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martin, Martin G., McConkie-Rosell, Allyn, McCormack, Colleen E., Might, Matthew, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina GS, Parker, Neil H., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Sampson, Jacinda B., Scott, Daryl A., Sharma, Prashant, Shashi, Vandana, Silverman, Edwin K., Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wan, Jijun, Wangler, Michael F., Ward, Patricia A., Wheeler, Matthew T., Wolfe, Lynne A., Worthey, Elizabeth A., Yamamoto, Shinya, Yang, Yaping, Yu, Guoyun, Zhao, Chunli, Zheng, Allison

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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder von Yoon, Wan Hee, Jangam, Sharayu, Davidson, Jean M., Grove, Megan E., Kohler, Jennefer N., Holmes, Matthew, Zhao, Chunli, Contrepois, Kévin, Heyman, Heino M., Webb-Robertson, Bobbie-Jo M., Alejandro, Mercedes E., Allard, Patrick, Balasubramanyam, Ashok, Barseghyan, Hayk, Bican, Anna, Birch, Camille L., Bostwick, Bret L., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dayal, Jyoti G., Dell’Angelica, Esteban C., Dorset, Daniel C., Draper, David D., Eckstein, David J., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Glanton, Emily, Godfrey, Rena A., Goldstein, David B., Gould, Sarah E., Gourdine, Jean-Philippe F., Hanchard, Neil A., Herzog, Matthew R., Hom, Jason, Howerton, Ellen M., Huang, Yong, Jacob, Howard J., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krier, Joel B., Lazar, Jozef, Lee, Hane, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, May, Thomas, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo M., Novacic, Donna, Orange, Jordan S., Palmer, Christina G.S., Potocki, Lorraine, Pusey, Barbara N., Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Samson, Susan L., Schoch, Kelly, Schroeder, Molly C., Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Spillmann, Rebecca C., Stong, Nicholas, Tifft, Cynthia J., Tran, Alyssa A., Valivullah, Zaheer M., Ward, Patricia A., Yamamoto, Shinya, Snyder, Michael, Merker, Jason D., Fisher, Paul G., Mayr, Johannes A., Morris, Andrew A., Schelley, Susan, Friederich, Marisa W., Yamamoto, Shinya, Wangler, Michael F., Taylor, Robert W., Bernstein, Jonathan A.

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Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia von Panman, JL, Venkatraghavan, V, van der Ende, EL, Steketee, RME, Jiskoot, LC, Poos, JM, Dopper, EGP, Meeter, LHH, Kaat, LD, Rombouts, SARB, Vernooij, MW, Kievit, AJA, Premi, E, Cosseddu, M, Bonomi, E, Olives, J, Rohrer, JD, Sanchez-Valle, R, Borroni, B, Bron, EE, Van Swieten, JC, Papma, JM, Klein, S

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Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia von Patel, Raihaan, Van Langenhove, Tim, Nielsen, Jørgen E., Remes, Anne M., Schroeter, Matthias L., Pasquier, Florence, Levin, Johannes, Le Ber, Isabelle, Vandenberghe, Rik, Moreno, Fermin, Sanchez‐Valle, Raquel, Gerhard, Alexander, Graff, Caroline, Sorbi, Sandro, Seelaar, Harro, Swieten, John C., Finger, Elizabeth, Tartaglia, Maria Carmela, Tiraboschi, Pietro, Galimberti, Daniela, Borroni, Barbara, Rowe, James B., Bocchetta, Martina, Rohrer, Jonathan D., Chakravarty, M. Mallar, Ducharme, Simon, Nelson, Annabel, Bouzigues, Arabella, Heller, Carolin, Greaves, Caroline V, Thomas, David L, Zetterberg, Henrik, Russell, Lucy L, Bocchetta, Martina, Convery, Rhian S, Cope, Thomas, Rittman, Timothy, Benussi, Alberto, Gasparotti, Roberto, Arighi, Andrea, Borracci, Vittoria, Rossi, Giacomina, Giaccone, Giorgio, Caroppo, Paola, Prioni, Sara, Tang‐Wai, David, Castelo‐Branco, Miguel, Keren, Ron, Black, Sandra, Bartha, Robart, Rademakers, Rosa, Poos, Jackie, Papma, Janne M., Giannini, Lucia, Pijnenburg, Yolande, Polito, Cristina, Lombardi, Gemma, Andersson, Christin, Öijerstedt, Linn, Jelic, Vesna, Lladó, Albert, Olives, Jaume, Balasa, Mircea, Bargalló, Nuria, Borrego‐Ecija, Sergi, Verdelho, Ana, Maruta, Carolina, Ferreira, Catarina B., Miltenberger, Gabriel, Couto, Frederico Simões, Gabilondo, Alazne, Gorostidi, Ana, Villanua, Jorge, Cañada, Marta, Tainta, Mikel, Barandiaran, Myriam, Bender, Benjamin, Wilke, Carlo, Graf, Lisa, Vogels, Annick, Van Damme, Philip, Poesen, Koen, Camuzat, Agnès, Brice, Alexis, Funkiewiez, Aurélie, Sayah, Sabrina, Wlasich, Elisabeth, Wagemann, Olivia, Hoegen, Tobias, Lombardi, Jolina, Anderl‐Straub, Sarah, Rollin, Adeline, Kuchcinski, Gregory, Lebouvier, Thibaud, Santiago, Beatriz, Leitão, Maria João, Almeida, Maria Rosario, Tábuas‐Pereira, Miguel, Afonso, Sónia, Polyakova, Maryna

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Apathy in presymptomatic genetic frontotemporal dementia predicts cognitive decline and is driven by structural brain changes von Malpetti, Maura, Jones, P. Simon, Tsvetanov, Kamen A., Rittman, Timothy, Swieten, John C., Borroni, Barbara, Sanchez‐Valle, Raquel, Moreno, Fermin, Laforce, Robert, Graff, Caroline, Synofzik, Matthis, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Finger, Elizabeth, Vandenberghe, Rik, Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Chris R., Gerhard, Alexander, Levin, Johannes, Danek, Adrian, Otto, Markus, Frisoni, Giovanni B., Ghidoni, Roberta, Sorbi, Sandro, Heller, Carolin, Todd, Emily G., Bocchetta, Martina, Cash, David M., Convery, Rhian S., Peakman, Georgia, Moore, Katrina M., Rohrer, Jonathan D., Kievit, Rogier A., Rowe, James B., (GENFI), Genetic FTD Initiative

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Longitudinal Cognitive Changes in Genetic Frontotemporal Dementia Within the GENFI Cohort von Poos, Jackie M., MacDougall, Amy, van den Berg, Esther, Jiskoot, Lize C., Papma, Janne M., van der Ende, Emma L., Seelaar, Harro, Russell, Lucy L., Peakman, Georgia, Convery, Rhian, Pijnenburg, Yolande A.L., Moreno, Fermin, Sanchez-Valle, Raquel, Borroni, Barbara, Laforce, Robert, Doré, Marie-Claire, Masellis, Mario, Tartaglia, Maria Carmela, Graff, Caroline, Galimberti, Daniela, Rowe, James B., Finger, Elizabeth, Synofzik, Matthis, Vandenberghe, Rik, Mendonça, Alexandre, Tiraboschi, Pietro, Santana, Isabel, Ducharme, Simon, Butler, Christopher, Gerhard, Alexander, Levin, Johannes, Danek, Adrian, Otto, Markus, Le Ber, Isabelle, Pasquier, Florence, van Swieten, John, Rohrer, Jonathan D.

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