Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
index medicus (134) 134
humans (124) 124
female (90) 90
clinical neurology (89) 89
male (88) 88
middle aged (67) 67
amyotrophic lateral sclerosis - genetics (58) 58
adult (55) 55
aged (54) 54
amyotrophic lateral sclerosis (54) 54
neurosciences (48) 48
life sciences (39) 39
abridged index medicus (38) 38
mutation (31) 31
neurology (31) 31
amyotrophic-lateral-sclerosis (28) 28
als (26) 26
aged, 80 and over (25) 25
animals (24) 24
adolescent (21) 21
gene (21) 21
pedigree (20) 20
santé publique et épidémiologie (20) 20
young adult (20) 20
anesthesiology (19) 19
mutations (19) 19
risk factors (19) 19
amyotrophic lateral sclerosis - epidemiology (18) 18
cohort studies (18) 18
genetic aspects (18) 18
genetics (18) 18
age of onset (17) 17
analysis (17) 17
genetics & heredity (17) 17
france - epidemiology (16) 16
mutation - genetics (16) 16
dna mutational analysis (15) 15
motor-neuron disease (15) 15
disease (14) 14
genotype (14) 14
superoxide dismutase - genetics (14) 14
dementia (13) 13
diagnosis (13) 13
disease progression (13) 13
neurons and cognition (13) 13
genes (12) 12
multiple sclerosis (12) 12
superoxide dismutase-1 (12) 12
survival (12) 12
tdp-43 (12) 12
phenotype (11) 11
double-blind method (10) 10
human health and pathology (10) 10
mice (10) 10
protein (10) 10
treatment outcome (10) 10
amyotrophic lateral sclerosis - pathology (9) 9
base sequence (9) 9
dna-binding proteins - genetics (9) 9
france (9) 9
genetic predisposition to disease - genetics (9) 9
hexanucleotide repeat (9) 9
medical and health sciences (9) 9
medicin och hälsovetenskap (9) 9
motor neurons (9) 9
research (9) 9
amyotrophic lateral sclerosis - metabolism (8) 8
biochemistry & molecular biology (8) 8
child (8) 8
criteria (8) 8
dose-response relationship, drug (8) 8
family health (8) 8
frontotemporal lobar degeneration (8) 8
genetic predisposition to disease (8) 8
genetic testing (8) 8
molecular sequence data (8) 8
mutation, missense (8) 8
nerve tissue proteins - genetics (8) 8
neurologi (8) 8
neurons (8) 8
alzheimers-disease (7) 7
amino acid sequence (7) 7
amyotrophic lateral sclerosis - diagnosis (7) 7
amyotrophic lateral sclerosis - etiology (7) 7
case-control studies (7) 7
cells, cultured (7) 7
clinical medicine (7) 7
clinical trials (7) 7
frontotemporal dementia (7) 7
gene frequency (7) 7
gene mutations (7) 7
genetic markers - genetics (7) 7
genetic research (7) 7
geriatrics & gerontology (7) 7
internal medicine (7) 7
klinisk medicin (7) 7
magnetic resonance imaging (7) 7
motor neuron disease (7) 7
nervous system diseases (7) 7
neurodegeneration (7) 7
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

by Kappos, Ludwig and Bar-Or, Amit and Cree, Bruce A C and Fox, Robert J and Giovannoni, Gavin and Gold, Ralf and Vermersch, Patrick and Arnold, Douglas L and Arnould, Sophie and Scherz, Tatiana and Wolf, Christian and Wallström, Erik and Dahlke, Frank and Achiron, Anat and Achtnichts, Lutz and Agan, Kadriye and Akman-Demir, Gulsen and Allen, Alison B and Antel, Jack P and Antiguedad, Alfredo Rodriguez and Apperson, Michelle and Applebee, Angela M and Ayuso, Guillermo Izquierdo and Baba, Masayuki and Bajenaru, Ovidiu and Balasa, Rodica and Balci, Belgin Petek and Barnett, Michael and Bass, Ann and Becker, Veit U and Bejinariu, Mihaela and Bergh, Florian Then and Bergmann, Arnfin and Bernitsas, Evanthia and Berthele, Achim and Bhan, Virender and Bischof, Felix and Bjork, Randall John and Blevins, Gregg and Boehringer, Matthias and Boerner, Thomas and Bonek, Robert and Bowen, James D and Bowling, Allen and Boyko, Alexey N and Boz, Cavit and Bracknies, Vera and Braune, Stefan and Brescia Morra, Vincenzo and Brochet, Bruno and Brola, Waldemar and Brownstone, Paul Kenneth and Brozman, Miroslav and Brunet, Donald and Buraga, Ioan and Burnett, Margaret and Buttmann, Mathias and Butzkueven, Helmut and Cahill, Jonathan and Calkwood, Jonathan C and Camu, William and Cascione, Mark and Castelnovo, Giovani and Centonze, Diego and Cerqueira, Joao and Chan, Andrew and Cimprichova, Andrea and Cohan, Stanley and Comi, Giancarlo and Conway, Jill and Cooper, Joanna A and Corboy, John and Correale, Jorge and Costell, Brian and Cottrell, David A and Coyle, Patricia K and Craner, Matthew and Cui, Liying and Cunha, Luis and Czlonkowska, Anna and da Silva, Ana Martins and de Sa, Joao and de Seze, Jérôme and Debouverie, Marc and Debruyne, Jan and Decoo, Danny and Defer, Gilles and Derfuss, Tobias and Deri, Norma H and Dihenia, Bhupesh and Dioszeghy, Peter and Donath, Vladimir and Dubois, Benedicte and Duddy, Martin and Duquette, Pierre and Edan, Gilles and Efendi, Husnu and Elias, Stanton and Emrich, Peter J and Estruch, Bonaventura Casanova and ... and EXPAND Clinical Investigators and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
The Lancet, ISSN 0140-6736, 03/2018, Volume 391, Issue 10127, pp. 1263 - 1273
Journal Article
by Nicolas, Aude and Kenna, Kevin P and Kenna, Aoife and Kenna, Kevin and Kenna, Brendan J and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Logullo, Francesco O and Simone, Isabella and Simone, Isabella L and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Cavallaro, Sebastiano and Mora, Gabriele and Mora, Jesús S and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Ricci, Claudia and Benigni, Michele and Cau, Tea B and ... and Genomic Translation ALS Care GTAC and ALS Sequencing Consortium and Clinical Res ALS Related Disorders and NYGC ALS Consortium and ITALSGEN Consortium and SLAGEN Consortium and French ALS Consortium and Project MinE ALS Sequencing Consor and Answer ALS Fdn and Project MinE ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Umeå universitet
Neuron, ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
Journal Article
by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M.C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A.C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and Di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and Wellcome Trust Case Control Consor and Int IBD Genetics Consortium IIBDGC and International Multiple Sclerosis Genetics Consortium (IMSGC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International IBD Genetics Consortium (IIBDGC) and Institutionen för fysik, kemi och biologi and Linköpings universitet and Bioinformatik and Tekniska högskolan
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 11, pp. 1353 - 1362
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, pp. e83406 - e83406
Journal Article
Journal Article