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101.
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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases. [electronic resource] by
- Lanoiselée, Hélène-Marie
- Nicolas, Gaël
- Wallon, David
- Rovelet-Lecrux, Anne
- Lacour, Morgane
- Rousseau, Stéphane
- Richard, Anne-Claire
- Pasquier, Florence
- Rollin-Sillaire, Adeline
- Martinaud, Olivier
- Quillard-Muraine, Muriel
- de la Sayette, Vincent
- Boutoleau-Bretonniere, Claire
- Etcharry-Bouyx, Frédérique
- Chauviré, Valérie
- Sarazin, Marie
- le Ber, Isabelle
- Epelbaum, Stéphane
- Jonveaux, Thérèse
- Rouaud, Olivier
- Ceccaldi, Mathieu
- Félician, Olivier
- Godefroy, Olivier
- Formaglio, Maite
- Croisile, Bernard
- Auriacombe, Sophie
- Chamard, Ludivine
- Vincent, Jean-Louis
- Sauvée, Mathilde
- Marelli-Tosi, Cecilia
- Gabelle, Audrey
- Ozsancak, Canan
- Pariente, Jérémie
- Paquet, Claire
- Hannequin, Didier
- Campion, Dominique
Producer: 20170612
In:
PLoS medicine vol. 14
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102.
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Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years. [electronic resource] by
- Lacour, Morgane
- Quenez, Olivier
- Rovelet-Lecrux, Anne
- Salomon, Bruno
- Rousseau, Stephane
- Richard, Anne-Claire
- Quillard-Muraine, Muriel
- Pasquier, Florence
- Rollin-Sillaire, Adeline
- Martinaud, Olivier
- Zarea, Aline
- de la Sayette, Vincent
- Boutoleau-Bretonniere, Claire
- Etcharry-Bouyx, Frédérique
- Chauviré, Valérie
- Sarazin, Marie
- le Ber, Isabelle
- Epelbaum, Stéphane
- Jonveaux, Thérèse
- Rouaud, Olivier
- Ceccaldi, Mathieu
- Godefroy, Olivier
- Formaglio, Maite
- Croisile, Bernard
- Auriacombe, Sophie
- Magnin, Eloi
- Sauvée, Mathilde
- Marelli, Cecilia
- Gabelle, Audrey
- Pariente, Jeremie
- Paquet, Claire
- Boland, Anne
- Deleuze, Jean-François
- Campion, Dominique
- Hannequin, Didier
- Nicolas, Gael
- Wallon, David
Producer: 20201013
In:
Journal of Alzheimer's disease : JAD vol. 71
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103.
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Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons. [electronic resource] by
- Nicolas, Gaël
- Wallon, David
- Charbonnier, Camille
- Quenez, Olivier
- Rousseau, Stéphane
- Richard, Anne-Claire
- Rovelet-Lecrux, Anne
- Coutant, Sophie
- Le Guennec, Kilan
- Bacq, Delphine
- Garnier, Jean-Guillaume
- Olaso, Robert
- Boland, Anne
- Meyer, Vincent
- Deleuze, Jean-François
- Munter, Hans Markus
- Bourque, Guillaume
- Auld, Daniel
- Montpetit, Alexandre
- Lathrop, Mark
- Guyant-Maréchal, Lucie
- Martinaud, Olivier
- Pariente, Jérémie
- Rollin-Sillaire, Adeline
- Pasquier, Florence
- Le Ber, Isabelle
- Sarazin, Marie
- Croisile, Bernard
- Boutoleau-Bretonnière, Claire
- Thomas-Antérion, Catherine
- Paquet, Claire
- Sauvée, Mathilde
- Moreaud, Olivier
- Gabelle, Audrey
- Sellal, François
- Ceccaldi, Mathieu
- Chamard, Ludivine
- Blanc, Frédéric
- Frebourg, Thierry
- Campion, Dominique
- Hannequin, Didier
Producer: 20161226
In:
European journal of human genetics : EJHG vol. 24
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104.
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Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders. [electronic resource] by
- Ducharme, Simon
- Dols, Annemiek
- Laforce, Robert
- Devenney, Emma
- Kumfor, Fiona
- van den Stock, Jan
- Dallaire-Théroux, Caroline
- Seelaar, Harro
- Gossink, Flora
- Vijverberg, Everard
- Huey, Edward
- Vandenbulcke, Mathieu
- Masellis, Mario
- Trieu, Calvin
- Onyike, Chiadi
- Caramelli, Paulo
- de Souza, Leonardo Cruz
- Santillo, Alexander
- Waldö, Maria Landqvist
- Landin-Romero, Ramon
- Piguet, Olivier
- Kelso, Wendy
- Eratne, Dhamidhu
- Velakoulis, Dennis
- Ikeda, Manabu
- Perry, David
- Pressman, Peter
- Boeve, Bradley
- Vandenberghe, Rik
- Mendez, Mario
- Azuar, Carole
- Levy, Richard
- Le Ber, Isabelle
- Baez, Sandra
- Lerner, Alan
- Ellajosyula, Ratnavalli
- Pasquier, Florence
- Galimberti, Daniela
- Scarpini, Elio
- van Swieten, John
- Hornberger, Michael
- Rosen, Howard
- Hodges, John
- Diehl-Schmid, Janine
- Pijnenburg, Yolande
Producer: 20210119
In:
Brain : a journal of neurology vol. 143
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105.
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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. [electronic resource] by
- Keller, Annika
- Westenberger, Ana
- Sobrido, Maria J
- García-Murias, Maria
- Domingo, Aloysius
- Sears, Renee L
- Lemos, Roberta R
- Ordoñez-Ugalde, Andres
- Nicolas, Gael
- da Cunha, José E Gomes
- Rushing, Elisabeth J
- Hugelshofer, Michael
- Wurnig, Moritz C
- Kaech, Andres
- Reimann, Regina
- Lohmann, Katja
- Dobričić, Valerija
- Carracedo, Angel
- Petrović, Igor
- Miyasaki, Janis M
- Abakumova, Irina
- Mäe, Maarja Andaloussi
- Raschperger, Elisabeth
- Zatz, Mayana
- Zschiedrich, Katja
- Klepper, Jörg
- Spiteri, Elizabeth
- Prieto, Jose M
- Navas, Inmaculada
- Preuss, Michael
- Dering, Carmen
- Janković, Milena
- Paucar, Martin
- Svenningsson, Per
- Saliminejad, Kioomars
- Khorshid, Hamid R K
- Novaković, Ivana
- Aguzzi, Adriano
- Boss, Andreas
- Le Ber, Isabelle
- Defer, Gilles
- Hannequin, Didier
- Kostić, Vladimir S
- Campion, Dominique
- Geschwind, Daniel H
- Coppola, Giovanni
- Betsholtz, Christer
- Klein, Christine
- Oliveira, Joao R M
Producer: 20131126
In:
Nature genetics vol. 45
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106.
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ATXN2 trinucleotide repeat length correlates with risk of ALS. [electronic resource] by
- Sproviero, William
- Shatunov, Aleksey
- Stahl, Daniel
- Shoai, Maryam
- van Rheenen, Wouter
- Jones, Ashley R
- Al-Sarraj, Safa
- Andersen, Peter M
- Bonini, Nancy M
- Conforti, Francesca L
- Van Damme, Philip
- Daoud, Hussein
- Del Mar Amador, Maria
- Fogh, Isabella
- Forzan, Monica
- Gaastra, Ben
- Gellera, Cinzia
- Gitler, Aaron D
- Hardy, John
- Fratta, Pietro
- La Bella, Vincenzo
- Le Ber, Isabelle
- Van Langenhove, Tim
- Lattante, Serena
- Lee, Yi-Chung
- Malaspina, Andrea
- Meininger, Vincent
- Millecamps, Stéphanie
- Orrell, Richard
- Rademakers, Rosa
- Robberecht, Wim
- Rouleau, Guy
- Ross, Owen A
- Salachas, Francois
- Sidle, Katie
- Smith, Bradley N
- Soong, Bing-Wen
- Sorarù, Gianni
- Stevanin, Giovanni
- Kabashi, Edor
- Troakes, Claire
- van Broeckhoven, Christine
- Veldink, Jan H
- van den Berg, Leonard H
- Shaw, Christopher E
- Powell, John F
- Al-Chalabi, Ammar
Producer: 20170928
In:
Neurobiology of aging vol. 51
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107.
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. [electronic resource] by
- Majounie, Elisa
- Renton, Alan E
- Mok, Kin
- Dopper, Elise G P
- Waite, Adrian
- Rollinson, Sara
- Chiò, Adriano
- Restagno, Gabriella
- Nicolaou, Nayia
- Simon-Sanchez, Javier
- van Swieten, John C
- Abramzon, Yevgeniya
- Johnson, Janel O
- Sendtner, Michael
- Pamphlett, Roger
- Orrell, Richard W
- Mead, Simon
- Sidle, Katie C
- Houlden, Henry
- Rohrer, Jonathan D
- Morrison, Karen E
- Pall, Hardev
- Talbot, Kevin
- Ansorge, Olaf
- Hernandez, Dena G
- Arepalli, Sampath
- Sabatelli, Mario
- Mora, Gabriele
- Corbo, Massimo
- Giannini, Fabio
- Calvo, Andrea
- Englund, Elisabet
- Borghero, Giuseppe
- Floris, Gian Luca
- Remes, Anne M
- Laaksovirta, Hannu
- McCluskey, Leo
- Trojanowski, John Q
- Van Deerlin, Vivianna M
- Schellenberg, Gerard D
- Nalls, Michael A
- Drory, Vivian E
- Lu, Chin-Song
- Yeh, Tu-Hsueh
- Ishiura, Hiroyuki
- Takahashi, Yuji
- Tsuji, Shoji
- Le Ber, Isabelle
- Brice, Alexis
- Drepper, Carsten
- Williams, Nigel
- Kirby, Janine
- Shaw, Pamela
- Hardy, John
- Tienari, Pentti J
- Heutink, Peter
- Morris, Huw R
- Pickering-Brown, Stuart
- Traynor, Bryan J
Producer: 20120511
In:
The Lancet. Neurology vol. 11
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108.
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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers. [electronic resource] by
- Zhang, Ming
- Ferrari, Raffaele
- Tartaglia, Maria Carmela
- Keith, Julia
- Surace, Ezequiel I
- Wolf, Uri
- Sato, Christine
- Grinberg, Mark
- Liang, Yan
- Xi, Zhengrui
- Dupont, Kyle
- McGoldrick, Philip
- Weichert, Anna
- McKeever, Paul M
- Schneider, Raphael
- McCorkindale, Michael D
- Manzoni, Claudia
- Rademakers, Rosa
- Graff-Radford, Neill R
- Dickson, Dennis W
- Parisi, Joseph E
- Boeve, Bradley F
- Petersen, Ronald C
- Miller, Bruce L
- Seeley, William W
- van Swieten, John C
- van Rooij, Jeroen
- Pijnenburg, Yolande
- van der Zee, Julie
- Van Broeckhoven, Christine
- Le Ber, Isabelle
- Van Deerlin, Vivianna
- Suh, EunRan
- Rohrer, Jonathan D
- Mead, Simon
- Graff, Caroline
- Öijerstedt, Linn
- Pickering-Brown, Stuart
- Rollinson, Sara
- Rossi, Giacomina
- Tagliavini, Fabrizio
- Brooks, William S
- Dobson-Stone, Carol
- Halliday, Glenda M
- Hodges, John R
- Piguet, Olivier
- Binetti, Giuliano
- Benussi, Luisa
- Ghidoni, Roberta
- Nacmias, Benedetta
- Sorbi, Sandro
- Bruni, Amalia C
- Galimberti, Daniela
- Scarpini, Elio
- Rainero, Innocenzo
- Rubino, Elisa
- Clarimon, Jordi
- Lleó, Alberto
- Ruiz, Agustin
- Hernández, Isabel
- Pastor, Pau
- Diez-Fairen, Monica
- Borroni, Barbara
- Pasquier, Florence
- Deramecourt, Vincent
- Lebouvier, Thibaud
- Perneczky, Robert
- Diehl-Schmid, Janine
- Grafman, Jordan
- Huey, Edward D
- Mayeux, Richard
- Nalls, Michael A
- Hernandez, Dena
- Singleton, Andrew
- Momeni, Parastoo
- Zeng, Zhen
- Hardy, John
- Robertson, Janice
- Zinman, Lorne
- Rogaeva, Ekaterina
Producer: 20190705
In:
Brain : a journal of neurology vol. 141
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109.
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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. [electronic resource] by
- Coppola, Giovanni
- Chinnathambi, Subashchandrabose
- Lee, Jason JiYong
- Dombroski, Beth A
- Baker, Matt C
- Soto-Ortolaza, Alexandra I
- Lee, Suzee E
- Klein, Eric
- Huang, Alden Y
- Sears, Renee
- Lane, Jessica R
- Karydas, Anna M
- Kenet, Robert O
- Biernat, Jacek
- Wang, Li-San
- Cotman, Carl W
- Decarli, Charles S
- Levey, Allan I
- Ringman, John M
- Mendez, Mario F
- Chui, Helena C
- Le Ber, Isabelle
- Brice, Alexis
- Lupton, Michelle K
- Preza, Elisavet
- Lovestone, Simon
- Powell, John
- Graff-Radford, Neill
- Petersen, Ronald C
- Boeve, Bradley F
- Lippa, Carol F
- Bigio, Eileen H
- Mackenzie, Ian
- Finger, Elizabeth
- Kertesz, Andrew
- Caselli, Richard J
- Gearing, Marla
- Juncos, Jorge L
- Ghetti, Bernardino
- Spina, Salvatore
- Bordelon, Yvette M
- Tourtellotte, Wallace W
- Frosch, Matthew P
- Vonsattel, Jean Paul G
- Zarow, Chris
- Beach, Thomas G
- Albin, Roger L
- Lieberman, Andrew P
- Lee, Virginia M
- Trojanowski, John Q
- Van Deerlin, Vivianna M
- Bird, Thomas D
- Galasko, Douglas R
- Masliah, Eliezer
- White, Charles L
- Troncoso, Juan C
- Hannequin, Didier
- Boxer, Adam L
- Geschwind, Michael D
- Kumar, Satish
- Mandelkow, Eva-Maria
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Dickson, Dennis W
- Haines, Jonathan L
- Mayeux, Richard
- Pericak-Vance, Margaret A
- Farrer, Lindsay A
- Ross, Owen A
- Rademakers, Rosa
- Schellenberg, Gerard D
- Miller, Bruce L
- Mandelkow, Eckhard
- Geschwind, Daniel H
Producer: 20130625
In:
Human molecular genetics vol. 21
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110.
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Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. [electronic resource] by
- Moore, Katrina M
- Nicholas, Jennifer
- Grossman, Murray
- McMillan, Corey T
- Irwin, David J
- Massimo, Lauren
- Van Deerlin, Vivianna M
- Warren, Jason D
- Fox, Nick C
- Rossor, Martin N
- Mead, Simon
- Bocchetta, Martina
- Boeve, Bradley F
- Knopman, David S
- Graff-Radford, Neill R
- Forsberg, Leah K
- Rademakers, Rosa
- Wszolek, Zbigniew K
- van Swieten, John C
- Jiskoot, Lize C
- Meeter, Lieke H
- Dopper, Elise Gp
- Papma, Janne M
- Snowden, Julie S
- Saxon, Jennifer
- Jones, Matthew
- Pickering-Brown, Stuart
- Le Ber, Isabelle
- Camuzat, Agnès
- Brice, Alexis
- Caroppo, Paola
- Ghidoni, Roberta
- Pievani, Michela
- Benussi, Luisa
- Binetti, Giuliano
- Dickerson, Bradford C
- Lucente, Diane
- Krivensky, Samantha
- Graff, Caroline
- Öijerstedt, Linn
- Fallström, Marie
- Thonberg, Håkan
- Ghoshal, Nupur
- Morris, John C
- Borroni, Barbara
- Benussi, Alberto
- Padovani, Alessandro
- Galimberti, Daniela
- Scarpini, Elio
- Fumagalli, Giorgio G
- Mackenzie, Ian R
- Hsiung, Ging-Yuek R
- Sengdy, Pheth
- Boxer, Adam L
- Rosen, Howie
- Taylor, Joanne B
- Synofzik, Matthis
- Wilke, Carlo
- Sulzer, Patricia
- Hodges, John R
- Halliday, Glenda
- Kwok, John
- Sanchez-Valle, Raquel
- Lladó, Albert
- Borrego-Ecija, Sergi
- Santana, Isabel
- Almeida, Maria Rosário
- Tábuas-Pereira, Miguel
- Moreno, Fermin
- Barandiaran, Myriam
- Indakoetxea, Begoña
- Levin, Johannes
- Danek, Adrian
- Rowe, James B
- Cope, Thomas E
- Otto, Markus
- Anderl-Straub, Sarah
- de Mendonça, Alexandre
- Maruta, Carolina
- Masellis, Mario
- Black, Sandra E
- Couratier, Philippe
- Lautrette, Geraldine
- Huey, Edward D
- Sorbi, Sandro
- Nacmias, Benedetta
- Laforce, Robert
- Tremblay, Marie-Pier L
- Vandenberghe, Rik
- Damme, Philip Van
- Rogalski, Emily J
- Weintraub, Sandra
- Gerhard, Alexander
- Onyike, Chiadi U
- Ducharme, Simon
- Papageorgiou, Sokratis G
- Ng, Adeline Su Lyn
- Brodtmann, Amy
- Finger, Elizabeth
- Guerreiro, Rita
- Bras, Jose
- Rohrer, Jonathan D
Producer: 20200715
In:
The Lancet. Neurology vol. 19
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111.
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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. [electronic resource] by
- Pottier, Cyril
- Zhou, Xiaolai
- Perkerson, Ralph B
- Baker, Matt
- Jenkins, Gregory D
- Serie, Daniel J
- Ghidoni, Roberta
- Benussi, Luisa
- Binetti, Giuliano
- López de Munain, Adolfo
- Zulaica, Miren
- Moreno, Fermin
- Le Ber, Isabelle
- Pasquier, Florence
- Hannequin, Didier
- Sánchez-Valle, Raquel
- Antonell, Anna
- Lladó, Albert
- Parsons, Tammee M
- Finch, NiCole A
- Finger, Elizabeth C
- Lippa, Carol F
- Huey, Edward D
- Neumann, Manuela
- Heutink, Peter
- Synofzik, Matthis
- Wilke, Carlo
- Rissman, Robert A
- Slawek, Jaroslaw
- Sitek, Emilia
- Johannsen, Peter
- Nielsen, Jørgen E
- Ren, Yingxue
- van Blitterswijk, Marka
- DeJesus-Hernandez, Mariely
- Christopher, Elizabeth
- Murray, Melissa E
- Bieniek, Kevin F
- Evers, Bret M
- Ferrari, Camilla
- Rollinson, Sara
- Richardson, Anna
- Scarpini, Elio
- Fumagalli, Giorgio G
- Padovani, Alessandro
- Hardy, John
- Momeni, Parastoo
- Ferrari, Raffaele
- Frangipane, Francesca
- Maletta, Raffaele
- Anfossi, Maria
- Gallo, Maura
- Petrucelli, Leonard
- Suh, EunRan
- Lopez, Oscar L
- Wong, Tsz H
- van Rooij, Jeroen G J
- Seelaar, Harro
- Mead, Simon
- Caselli, Richard J
- Reiman, Eric M
- Noel Sabbagh, Marwan
- Kjolby, Mads
- Nykjaer, Anders
- Karydas, Anna M
- Boxer, Adam L
- Grinberg, Lea T
- Grafman, Jordan
- Spina, Salvatore
- Oblak, Adrian
- Mesulam, M-Marsel
- Weintraub, Sandra
- Geula, Changiz
- Hodges, John R
- Piguet, Olivier
- Brooks, William S
- Irwin, David J
- Trojanowski, John Q
- Lee, Edward B
- Josephs, Keith A
- Parisi, Joseph E
- Ertekin-Taner, Nilüfer
- Knopman, David S
- Nacmias, Benedetta
- Piaceri, Irene
- Bagnoli, Silvia
- Sorbi, Sandro
- Gearing, Marla
- Glass, Jonathan
- Beach, Thomas G
- Black, Sandra E
- Masellis, Mario
- Rogaeva, Ekaterina
- Vonsattel, Jean-Paul
- Honig, Lawrence S
- Kofler, Julia
- Bruni, Amalia C
- Snowden, Julie
- Mann, David
- Pickering-Brown, Stuart
- Diehl-Schmid, Janine
- Winkelmann, Juliane
- Galimberti, Daniela
- Graff, Caroline
- Öijerstedt, Linn
- Troakes, Claire
- Al-Sarraj, Safa
- Cruchaga, Carlos
- Cairns, Nigel J
- Rohrer, Jonathan D
- Halliday, Glenda M
- Kwok, John B
- van Swieten, John C
- White, Charles L
- Ghetti, Bernardino
- Murell, Jill R
- Mackenzie, Ian R A
- Hsiung, Ging-Yuek R
- Borroni, Barbara
- Rossi, Giacomina
- Tagliavini, Fabrizio
- Wszolek, Zbigniew K
- Petersen, Ronald C
- Bigio, Eileen H
- Grossman, Murray
- Van Deerlin, Vivianna M
- Seeley, William W
- Miller, Bruce L
- Graff-Radford, Neill R
- Boeve, Bradley F
- Dickson, Dennis W
- Biernacka, Joanna M
- Rademakers, Rosa
Producer: 20190321
In:
The Lancet. Neurology vol. 17
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112.
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Frontotemporal dementia and its subtypes: a genome-wide association study. [electronic resource] by
- Ferrari, Raffaele
- Hernandez, Dena G
- Nalls, Michael A
- Rohrer, Jonathan D
- Ramasamy, Adaikalavan
- Kwok, John B J
- Dobson-Stone, Carol
- Brooks, William S
- Schofield, Peter R
- Halliday, Glenda M
- Hodges, John R
- Piguet, Olivier
- Bartley, Lauren
- Thompson, Elizabeth
- Haan, Eric
- Hernández, Isabel
- Ruiz, Agustín
- Boada, Mercè
- Borroni, Barbara
- Padovani, Alessandro
- Cruchaga, Carlos
- Cairns, Nigel J
- Benussi, Luisa
- Binetti, Giuliano
- Ghidoni, Roberta
- Forloni, Gianluigi
- Galimberti, Daniela
- Fenoglio, Chiara
- Serpente, Maria
- Scarpini, Elio
- Clarimón, Jordi
- Lleó, Alberto
- Blesa, Rafael
- Waldö, Maria Landqvist
- Nilsson, Karin
- Nilsson, Christer
- Mackenzie, Ian R A
- Hsiung, Ging-Yuek R
- Mann, David M A
- Grafman, Jordan
- Morris, Christopher M
- Attems, Johannes
- Griffiths, Timothy D
- McKeith, Ian G
- Thomas, Alan J
- Pietrini, P
- Huey, Edward D
- Wassermann, Eric M
- Baborie, Atik
- Jaros, Evelyn
- Tierney, Michael C
- Pastor, Pau
- Razquin, Cristina
- Ortega-Cubero, Sara
- Alonso, Elena
- Perneczky, Robert
- Diehl-Schmid, Janine
- Alexopoulos, Panagiotis
- Kurz, Alexander
- Rainero, Innocenzo
- Rubino, Elisa
- Pinessi, Lorenzo
- Rogaeva, Ekaterina
- St George-Hyslop, Peter
- Rossi, Giacomina
- Tagliavini, Fabrizio
- Giaccone, Giorgio
- Rowe, James B
- Schlachetzki, Johannes C M
- Uphill, James
- Collinge, John
- Mead, Simon
- Danek, Adrian
- Van Deerlin, Vivianna M
- Grossman, Murray
- Trojanowski, John Q
- van der Zee, Julie
- Deschamps, William
- Van Langenhove, Tim
- Cruts, Marc
- Van Broeckhoven, Christine
- Cappa, Stefano F
- Le Ber, Isabelle
- Hannequin, Didier
- Golfier, Véronique
- Vercelletto, Martine
- Brice, Alexis
- Nacmias, Benedetta
- Sorbi, Sandro
- Bagnoli, Silvia
- Piaceri, Irene
- Nielsen, Jørgen E
- Hjermind, Lena E
- Riemenschneider, Matthias
- Mayhaus, Manuel
- Ibach, Bernd
- Gasparoni, Gilles
- Pichler, Sabrina
- Gu, Wei
- Rossor, Martin N
- Fox, Nick C
- Warren, Jason D
- Spillantini, Maria Grazia
- Morris, Huw R
- Rizzu, Patrizia
- Heutink, Peter
- Snowden, Julie S
- Rollinson, Sara
- Richardson, Anna
- Gerhard, Alexander
- Bruni, Amalia C
- Maletta, Raffaele
- Frangipane, Francesca
- Cupidi, Chiara
- Bernardi, Livia
- Anfossi, Maria
- Gallo, Maura
- Conidi, Maria Elena
- Smirne, Nicoletta
- Rademakers, Rosa
- Baker, Matt
- Dickson, Dennis W
- Graff-Radford, Neill R
- Petersen, Ronald C
- Knopman, David
- Josephs, Keith A
- Boeve, Bradley F
- Parisi, Joseph E
- Seeley, William W
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- Scheltens, Philip
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- Puca, Annibale A
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- Milan, Graziella
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Producer: 20140811
In:
The Lancet. Neurology vol. 13
Availability: No items available.
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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. [electronic resource] by
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Producer: 20190715
In:
Neuron vol. 97
Availability: No items available.
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