A Model of the Optimal Tax Mix Including Capital Taxation von Revesz, John

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A Numerical Model of Optimal Differentiated Indirect Taxation von Revesz, John T

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Optimal indirect taxation and the uniformity debate: A review of theoretical results and empirical contributions von Nygård, Odd Erik, Revesz, John T.

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Optimal indirect taxation and the uniformity debate: A review of theoretical results and empirical contributions von Nygård, Odd Erik, Revesz, John T

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A literature review on optimal indirect taxation and the uniformity debate von Nygard, Odd E., Revesz, John T.

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The Spread of Neurodegenerative Disease von Hardy, John, Revesz, Tamas

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Correction to: A Model of the Optimal Tax Mix Including Capital Taxation von Revesz, John

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C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis von Rohrer, Jonathan D, Dr, Isaacs, Adrian M, PhD, Mizielinska, Sarah, PhD, Mead, Simon, Prof, Lashley, Tammaryn, PhD, Wray, Selina, PhD, Sidle, Katie, PhD, Fratta, Pietro, PhD, Orrell, Richard W, MD, Hardy, John, Prof, Holton, Janice, PhD, Revesz, Tamas, Prof, Rossor, Martin N, Prof, Warren, Jason D, Prof

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Age-dependent formation of TMEM106B amyloid filaments in human brains von Schweighauser, Manuel, Arseni, Diana, Bacioglu, Mehtap, Huang, Melissa, Lövestam, Sofia, Shi, Yang, Yang, Yang, Zhang, Wenjuan, Kotecha, Abhay, Garringer, Holly J., Vidal, Ruben, Hallinan, Grace I., Newell, Kathy L., Tarutani, Airi, Murayama, Shigeo, Miyazaki, Masayuki, Saito, Yuko, Yoshida, Mari, Hasegawa, Kazuko, Lashley, Tammaryn, Revesz, Tamas, Kovacs, Gabor G., van Swieten, John, Takao, Masaki, Hasegawa, Masato, Ghetti, Bernardino, Spillantini, Maria Grazia, Ryskeldi-Falcon, Benjamin, Murzin, Alexey G., Goedert, Michel, Scheres, Sjors H. W.

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Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study von Guerreiro, Rita, Ross, Owen A, Kun-Rodrigues, Celia, Hernandez, Dena G, Orme, Tatiana, Eicher, John D, Shepherd, Claire E, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G, Scholz, Sonja W, Troncoso, Juan C, Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E, Beach, Thomas G, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F, Petersen, Ronald C, Ferman, Tanis J, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J, Morris, John C, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M, Hardy, John, Trojanowski, John Q, Dickson, Dennis W, Singleton, Andrew, Stone, David J, Bras, Jose

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Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration von Rohrer, Jonathan D., Lashley, Tammaryn, Schott, Jonathan M., Warren, Jane E., Mead, Simon, Isaacs, Adrian M., Beck, Jonathan, Hardy, John, de Silva, Rohan, Warrington, Elizabeth, Troakes, Claire, Al-Sarraj, Safa, King, Andrew, Borroni, Barbara, Clarkson, Matthew J., Ourselin, Sebastien, Holton, Janice L., Fox, Nick C., Revesz, Tamas, Rossor, Martin N., Warren, Jason D.

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Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology von Ling, Helen, Kovacs, Gabor G, Vonsattel, Jean Paul G, Davey, Karen, Mok, Kin Y, Hardy, John, Morris, Huw R, Warner, Thomas T, Holton, Janice L, Revesz, Tamas

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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features von MAHONEY, Colin J, BECK, Jon, ROSSOR, Martin N, HARDY, John, COLLINGE, John, REVESZ, Tamas, MEAD, Simon, WARREN, Jason D, ROHRER, Jonathan D, LASHLEY, Tammaryn, MOK, Kin, SHAKESPEARE, Tim, YEATMAN, Tom, WARRINGTON, Elizabeth K, SCHOTT, Jonathan M, FOX, Nick C

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Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome von Jabbari, Edwin, Holland, Negin, Chelban, Viorica, Jones, P. Simon, Lamb, Ruth, Rawlinson, Charlotte, Guo, Tong, Costantini, Alyssa A, Tan, Manuela M. X, Heslegrave, Amanda J, Roncaroli, Federico, Klein, Johannes C, Ansorge, Olaf, Allinson, Kieren S. J, Jaunmuktane, Zane, Holton, Janice L, Revesz, Tamas, Warner, Thomas T, Lees, Andrew J, Zetterberg, Henrik, Russell, Lucy L, Bocchetta, Martina, Rohrer, Jonathan D, Williams, Nigel M, Grosset, Donald G, Burn, David J, Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, Hu, Michele T. M, Woodside, John, Houlden, Henry, Rowe, James B, Morris, Huw R

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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study von Jabbari, Edwin, Koga, Shunsuke, Valentino, Rebecca R, Reynolds, Regina H, Ferrari, Raffaele, Tan, Manuela M X, Rowe, James B, Dalgard, Clifton L, Scholz, Sonja W, Dickson, Dennis W, Warner, Thomas T, Revesz, Tamas, Höglinger, Günter U, Ross, Owen A, Ryten, Mina, Hardy, John, Shoai, Maryam, Morris, Huw R, Mok, Kin Y., Murphy, David P., Al-Sarraj, Safa, Troakes, Claire, Gentleman, Steve M., Allinson, Kieren S.J., Jaunmuktane, Zane, Holton, Janice L., Lees, Andrew J., Morris, Christopher M., Compta, Yaroslau, Gelpi, Ellen, van Swieten, John C., Rajput, Alex, Ferguson, Leslie, Cookson, Mark R., Gibbs, J. Raphael, Blauwendraat, Cornelis, Ding, Jinhui, Chia, Ruth, Traynor, Bryan J., Pantelyat, Alexander, Viollet, Coralie, Pletnikova, Olga, Troncoso, Juan C., Rosenthal, Liana S., Boxer, Adam L., Respondek, Gesine, Arzberger, Thomas, Roeber, Sigrun, Giese, Armin, Burn, David J., Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, T.M. Hu, Michele

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The genetics of Parkinson's syndromes: a critical review von Hardy, John, Lewis, Patrick, Revesz, Tamas, Lees, Andrew, Paisan-Ruiz, Coro

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Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease von Neumann, Juliane, Bras, Jose, Deas, Emma, O'Sullivan, Sean S., Parkkinen, Laura, Lachmann, Robin H., Li, Abi, Holton, Janice, Guerreiro, Rita, Paudel, Reema, Segarane, Badmavady, Singleton, Andrew, Lees, Andrew, Hardy, John, Houlden, Henry, Revesz, Tamas, Wood, Nicholas W.

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A common LRRK2 mutation in idiopathic Parkinson's disease von Gilks, William P, Abou-Sleiman, Patrick M, Gandhi, Sonia, Jain, Shushant, Singleton, Andrew, Lees, Andrew J, Shaw, Karen, Bhatia, Kailash P, Bonifati, Vincenzo, Quinn, Niall P, Lynch, John, Healy, Daniel G, Holton, Janice L, Revesz, Tamas, Wood, Nicholas W

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Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update von Mackenzie, Ian R. A., Neumann, Manuela, Bigio, Eileen H., Cairns, Nigel J., Alafuzoff, Irina, Kril, Jillian, Kovacs, Gabor G., Ghetti, Bernardino, Halliday, Glenda, Holm, Ida E., Ince, Paul G., Kamphorst, Wouter, Revesz, Tamas, Rozemuller, Annemieke J. M., Kumar-Singh, Samir, Akiyama, Haruhiko, Baborie, Atik, Spina, Salvatore, Dickson, Dennis W., Trojanowski, John Q., Mann, David M. A.

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Pembrolizumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma von Rini, Brian I, Plimack, Elizabeth R, Stus, Viktor, Gafanov, Rustem, Hawkins, Robert, Nosov, Dmitry, Pouliot, Frédéric, Alekseev, Boris, Soulières, Denis, Melichar, Bohuslav, Vynnychenko, Ihor, Kryzhanivska, Anna, Bondarenko, Igor, Azevedo, Sergio J, Borchiellini, Delphine, Szczylik, Cezary, Markus, Maurice, McDermott, Raymond S, Bedke, Jens, Tartas, Sophie, Chang, Yen-Hwa, Tamada, Satoshi, Shou, Qiong, Perini, Rodolfo F, Chen, Mei, Atkins, Michael B, Powles, Thomas

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