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Clinical testing panels for ALS: global distribution, consistency, and challenges
Author: Dilliott, Allison A.; Al Nasser, Ahmad; Elnagheeb, Marwa; Fifita, Jennifer; Henden, Lyndal; Keseler, Ingrid M.; Lenz, Steven; Marriott, Heather; Mccann, Emily; Mesaros, Maysen; Opie-Martin, Sarah; Owens, Emma; Palus, Brooke; Ross, Justyne; Wang, Zhanjun; White, Hannah; Al-Chalabi, Ammar; Andersen, Peter M.; Benatar, Michael; Blair, Ian; Cooper-Knock, Johnathan; Harrington, Elizabeth A.; Heckmann, Jeannine; Landers, John; Moreno, Cristiane; Nel, Melissa; Rampersaud, Evadnie; Roggenbuck, Jennifer; Rouleau, Guy; Traynor, Bryan; Van Blitterswijk, Marka; Van Rheenen, Wouter; Veldink, Jan; Weishaupt, Jochen; Drury, Luke; Harms, Matthew B.; Farhan, Sali M. K.
Journal: AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION. 2023; Vol. , Issue , pp. -. DOI: 10.1080/21678421.2023.2173015
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Associations between neuropsychiatric symptoms and cognition in Chinese patients with amyotrophic lateral sclerosis.
Author: Wei Q, Chen X, Cao B, Ou R, Zhao B, Wu Y, Shang H.
Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jul-Aug;17(5-6):358-65. doi: 10.3109/21678421.2016.1154574. Epub 2016 Mar 10.
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Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin.
Author: Zou ZY, Liu MS, Li XG, Cui LY.
Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Apr-May;17(3-4):249-52. doi: 10.3109/21678421.2016.1143012. Epub 2016 Mar 14.
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CHCHD10 is not a frequent causative gene in Chinese ALS patients.
Author: Li XL, Shu S, Li XG, Liu Q, Liu F, Cui B, Liu MS, Peng B, Cui LY, Zhang X.
Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jul-Aug;17(5-6):458-60. doi: 10.3109/21678421.2016.1170151. Epub 2016 Apr 14.
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Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.
Author: Shu S, Li XL, Liu Q, Liu F, Cui B, Liu MS, Cui LY, Li XG, Zhang X.
Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jun 3:1-3. [Epub ahead of print]
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H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression.
Author: Zou ZY, Liu MS, Li XG, Cui LY.
Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jun 27:1-4. [Epub ahead of print]
