91. ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia. (June 2018) Authors: Zhang, Kang; Liu, Qing; Liu, Keqiang; Shen, Dongchao; Tai, Hongfei; Shu, Shi; Ding, Qingyun; Fu, Hanhui; Liu, Shuangwu; Wang, Zhili; Li, Xiaoguang; Liu, Mingsheng; Zhang, Xue; Cui, Liying Journal: Neurology Issue: Volume 4:Number 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
92. AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?. (February 2018) Authors: Roubertie, Agathe; Hieu, Nelson; Roux, Charles-Joris; Leboucq, Nicolas; Manes, Gael; Charif, Majida; Echenne, Bernard; Goizet, Cyril; Guissart, Claire; Meyer, Pierre; Marelli, Cecilia; Rivier, François; Burglen, Lydie; Horvath, Rita; Hamel, Christian P.; Lenaers, Guy Journal: Neurology Issue: Volume 4:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
93. APOE polymorphisms influence longitudinal lipid trends preceding intracerebral hemorrhage. (August 2016) Authors: Phuah, Chia-Ling; Raffeld, Miriam R.; Ayres, Alison M.; Gurol, M. Edip; Viswanathan, Anand; Greenberg, Steven M.; Biffi, Alessandro; Rosand, Jonathan; Anderson, Christopher D. Journal: Neurology Issue: Volume 2:Number 4(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
94. APOE ϵ4 modifies the relationship between infectious burden and poor cognition. (August 2020) Authors: Zhao, Chen; Strobino, Kevin; Moon, Yeseon Park; Cheung, Ying Kuen; Sacco, Ralph L.; Stern, Yaakov; Elkind, Mitchell S.V. Journal: Neurology Issue: Volume 6:Number 4(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
95. Are migraineurs naturally born "well-hearted"?. (June 2015) Authors: Ducros, Anne Journal: Neurology Issue: Volume 1:Number 1(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
96. ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansion. (October 2017) Authors: Farhan, Sali M.K.; Gendron, Tania F.; Petrucelli, Leonard; Hegele, Robert A.; Strong, Michael J. Journal: Neurology Issue: Volume 3:Number 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
97. ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. (June 2017) Authors: Alber, Michael; Kalscheuer, Vera M.; Marco, Elysa; Sherr, Elliott; Lesca, Gaetan; Till, Marianne; Gradek, Gyri; Wiesener, Antje; Korenke, Christoph; Mercier, Sandra; Becker, Felicitas; Yamamoto, Toshiyuki; Scherer, Stephen W.; Marshall, Christian R.; Walker, Susan; Dutta, Usha R.; Dalal, Ashwin B... Journal: Neurology Issue: Volume 3:Number 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
98. ARHGEF9 mutations cause a specific recognizable X-linked intellectual disability syndrome. (June 2017) Authors: Striano, Pasquale; Zara, Federico Journal: Neurology Issue: Volume 3:Number 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
99. ASFMR1 splice variant: A predictor of fragile X-associated tremor/ataxia syndrome. (August 2018) Authors: Vittal, Padmaja; Pandya, Shrikant; Sharp, Kevin; Berry-Kravis, Elizabeth; Zhou, Lili; Ouyang, Bichun; Jackson, Jonathan; Hall, Deborah A. Journal: Neurology Issue: Volume 4:Number 4(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
100. Association Between Polymorphisms in Genes Encoding Methylenetetrahydrofolate Reductase and the Risk of Ménière's Disease. (June 2013) Authors: Huang, Yang; Teranishi, Masaaki; Uchida, Yasue; Nishio, Naoki; Kato, Ken; Otake, Hironao; Yoshida, Tadao; Sone, Michihiko; Sugiura, Saiko; Ando, Fujiko; Shimokata, Hiroshi; Nakashima, Tsutomu Journal: Journal of neurogenetics Issue: Volume 27:Number 1/2(2013) Page Start: 5 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗