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JAMA Neurology, ISSN 2168-6149, 10/2015, Volume 72, Issue 10, pp. 1155 - 1155
Because dietary intake may influence pathophysiologic mechanisms in sporadic amyotrophic lateral sclerosis (ALS), the association between premorbid dietary... 
Journal Article
Muscle and Nerve, ISSN 0148-639X, 2010, Volume 41, Issue 1, pp. 32 - 41
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 01/2012, Volume 83, Issue 4, pp. 383 - 388
OBJECTIVES: Amyotrophic lateral sclerosis (ALS) is a fatal disease characterised by combined upper and lower motor neuron degeneration. An early and accurate... 
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0007-1161, 04/2012, Volume 83, Issue 4, p. 383
ObjectivesAmyotrophic lateral sclerosis (ALS) is a fatal disease characterised by combined upper and lower motor neuron degeneration. An early and accurate... 
Journal Article
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2012, Volume 8, Issue 4, pp. P106 - P107
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 01/2011, Volume 82, Issue 10, pp. 1165 - 1170
BACKGROUND: Variation in the incidence rate in epidemiological studies on amyotrophic lateral sclerosis (ALS) may be due to a small population size and under... 
Journal Article
Amyotrophic lateral sclerosis and frontotemporal degeneration, ISSN 2167-8421, 04/2013, Volume 14, Issue 3, pp. 224 - 227
Sporadic ALS is a multifactorial disease for which there are probably multiple genetic risk factors. An association with increased parental age might suggest... 
Journal Article
Annals of Clinical and Translational Neurology, 02/2016, Volume 3, Issue 2, pp. 146 - 149
LRSAM1 mutations have been found in recessive and dominant forms of Charcot–Marie–Tooth disease. Within one generation of the original Dutch family in which... 
Proteins | Walking | Legs | Parkinsons disease | Mutation | Autophagy | Age
Journal Article
by Helbig, Ingo and Helbig, Katherine L and Lauerer, Robert J and Bahr, Jacqueline C and Souza, Ivana A and Myers, Candace T and Uysal, Betül and Schwarz, Niklas and Gandini, Maria A and Huang, Sun and Keren, Boris and Mignot, Cyril and Afenjar, Alexandra and Billette de Villemeur, Thierry and Héron, Delphine and Nava, Caroline and Valence, Stéphanie and Buratti, Julien and Fagerberg, Christina R and Soerensen, Kristina P and Kibaek, Maria and Kamsteeg, Erik-Jan and Koolen, David A and Gunning, Boudewijn and Schelhaas, H. Jurgen and Kruer, Michael C and Fox, Jordana and Bakhtiari, Somayeh and Jarrar, Randa and Padilla-Lopez, Sergio and Lindstrom, Kristin and Jin, Sheng Chih and Zeng, Xue and Bilguvar, Kaya and Papavasileiou, Antigone and Xing, Qinghe and Zhu, Changlian and Boysen, Katja and Vairo, Filippo and Lanpher, Brendan C and Klee, Eric W and Tillema, Jan-Mendelt and Payne, Eric T and Cousin, Margot A and Kruisselbrink, Teresa M and Wick, Myra J and Baker, Joshua and Haan, Eric and Smith, Nicholas and Smith, Lacey A and Smith, Edward and Sadeghpour, Azita and Davis, Erica E and Katsanis, Nicholas and Katsanis, Sara and Allori, Alexander and Angrist, Misha and Ashley, Patricia and Bidegain, Margarita and Boyd, Brita and Chambers, Eileen and Cope, Heidi and Cotten, C. Michael and Curington, Theresa and Ellestad, Sarah and Fisher, Kimberley and French, Amanda and Gallentine, William and Goldberg, Ronald and Hill, Kevin and Kansagra, Sujay and Kurtzberg, Joanne and Marcus, Jeffrey and McDonald, Marie and Mikati, Mohammed and Miller, Stephen and Murtha, Amy and Perilla, Yezmin and Pizoli, Carolyn and Purves, Todd and Ross, Sherry and Wiener, John and Corbett, Mark A and MacLennan, Alastair H and Gecz, Jozef and Biskup, Saskia and Goldmann, Eva and Rodan, Lance H and Kichula, Elizabeth and Segal, Eric and Jackson, Kelly E and Asamoah, Alexander and Dimmock, David and McCarrier, Julie and Botto, Lorenzo D and Filloux, Francis and Tvrdik, Tatiana and Cascino, Gregory D and Klingerman, Sherry and Neumann, Catherine and ... and Deciphering Dev Disorders Study and Deciphering Developmental Disorders Study 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 American Journal of Human Genetics, ISSN 0002-9297, 11/2018, Volume 103, Issue 5, pp. 666 - 678
Journal Article
Journal Article