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Accounting Historians Journal, ISSN 0148-4184, 08/2019
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2016, Volume 22, Issue 12, pp. 1402 - 1410
Journal Article
by Cirulli, Elizabeth T and Lasseigne, Brittany N and Petrovski, Slavé and Sapp, Peter C and Dion, Patrick A and Leblond, Claire S and Couthouis, Julien and Lu, Yi-Fan and Wang, Quanli and Krueger, Brian J and Ren, Zhong and Keebler, Jonathan and Han, Yujun and Levy, Shawn E and Boone, Braden E and Wimbish, Jack R and Waite, Lindsay L and Jones, Angela L and Carulli, John P and Day-Williams, Aaron G and Staropoli, John F and Xin, Winnie W and Chesi, Alessana and Raphael, Alya R and McKenna-Yasek, Diane and Cady, Janet and de Jong, J. M. B. Vianney and Kenna, Kevin P and Smith, Bradley N and Topp, Simon and Miller, Jack and Gkazi, Athina and Al-Chalabi, Ammar and van den Berg, Leonard H and Veldink, Jan and Silani, Vincenzo and Ticozzi, Nicola and Shaw, Christopher E and Baloh, Robert H and Appel, Stanley and Simpson, Ericka and Lagier-Tourenne, Clotilde and Pulst, Stefan M and Gibson, Summer and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Grossman, Murray and Shneider, Neil A and Chung, Wendy K and Ravits, John M and Glass, Jonathan D and Sims, Katherine B and van Deerlin, Vivianna M and Maniatis, Tom and Hayes, Sebastian D and Ordureau, Alban and Swarup, Sharan and Landers, John and Baas, Frank and Allen, Anew S and Bedlack, Richard S and Harper, J. Wade and Gitler, Aaron D and Rouleau, Guy A and Brown, Robert and Harms, Matthew B and Cooper, Gregory M and Harris, Tim and Myers, Richard M and Goldstein, David B and Hardiman, Orla and McLaughlin, Russell L and Mazzini, Letizia and Blair, Ian P and Williams, Kelly L and Nicholson, Garth A and Al-Sarraj, Safa and King, Anew and Scotter, Emma L and Troakes, Claire and Vance, Caroline and D'alfonso, Sana and Duga, Stefano and Corrado, Lucia and ten Asbroek, Anneloor L. M. A and Calini, Daniela and Colombrita, Claudia and Ratti, Antonia and Tiloca, Cinzia and Wu, Zheyang and Asress, Seneshaw and Polak, Meraida and Diekstra, Frank and van Rheenen, Wouter and Danielson, Eric W and Fallini, Claudia and Keagle, Pamela and Lewis, Elizabeth A and Kost, Jason and ... and FALS Sequencing Consortium
Science, ISSN 0036-8075, 2015, Volume 347, Issue 6229, pp. 1436 - 1441
Journal Article
Science, ISSN 0036-8075, 2/2009, Volume 323, Issue 5918, pp. 1208 - 1211
Journal Article
Science, ISSN 0036-8075, 3/2008, Volume 319, Issue 5870, pp. 1668 - 1672
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2012, Volume 33, Issue 10, pp. 2527.e3 - 2527.e10
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 2015, Volume 25, pp. 62 - 64
Abstract The diagnosis of cervical dystonia (CD) is based on physical examination and is therefore reliant on clinician experience. Due to variability of... 
Neurology | Delay to diagnosis | Cervical dystonia | Diagnosis | PREVALENCE | NEUROSCIENCES | CLINICAL NEUROLOGY | Time Factors | Physicians | Torticollis - diagnosis | Humans | Middle Aged | Female | Surveys and Questionnaires | Referral and Consultation - statistics & numerical data | Delayed Diagnosis - statistics & numerical data | Medical personnel | Dystonia
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, pp. 20881 - 20890
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Aggregation | Proteins | Yeasts | Nervous system diseases | Neurodegenerative diseases | Neurons | Drosophila | Prions | Amyotrophic lateral sclerosis | Genetic mutation | WILD-TYPE | TDP-43 PROTEINOPATHY | DROSOPHILA MODEL | MULTIDISCIPLINARY SCIENCES | NEURODEGENERATION | AMYLOID PORES | TOXICITY | AMYOTROPHIC-LATERAL-SCLEROSIS | FUS MUTATIONS | FRONTOTEMPORAL LOBAR DEGENERATION | AGGREGATION | Immunohistochemistry | Protein Structure, Tertiary | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Saccharomyces cerevisiae - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Cells, Cultured | Computational Biology | Genetic Association Studies - methods | TATA-Binding Protein Associated Factors - genetics | Drosophila melanogaster - genetics | Mutation, Missense - genetics | Motor Neurons - metabolism | Animals | Spinal Cord - cytology | Yeast fungi | Gene mutations | Physiological aspects | Development and progression | Genetic aspects | Research | Binding proteins | Health aspects | Biological Sciences | amyotrophic-lateral-sclerosis; frontotemporal lobar degeneration; drosophila model; fus mutations; tdp-43 proteinopathy; amyloid pores; wild-type; toxicity; neurodegeneration; aggregation | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Internal Medicine Journal, ISSN 1444-0903, 04/2018, Volume 48, Issue 4, pp. 469 - 471
Journal Article
Journal Article