151. C9orf72 and the Care of the Patient With ALS or FTD: Progress and Recommendations After 10 Years. (February 2021) Authors: Roggenbuck, Jennifer Journal: Neurology Issue: Volume 7:Number 1(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
152. Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls. (June 2017) Authors: Reimann, Jens; Lehmann, Diana; Hardy, Steven A.; Falkous, Gavin; Knowles, Charlotte V.Y.; Jones, Rachel L.; Kunz, Wolfram S.; Taylor, Robert W.; Kornblum, Cornelia 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) ↗
153. Can Anti–β-amyloid Monoclonal Antibodies Work in Autosomal Dominant Alzheimer Disease?. (February 2021) Authors: Imbimbo, Bruno P.; Lucca, Ugo; Watling, Mark Journal: Neurology Issue: Volume 7:Number 1(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
154. Carey-Fineman-Ziter syndrome with mutations in the myomaker gene and muscle fiber hypertrophy. (August 2018) Authors: Hedberg-Oldfors, Carola; Lindberg, Christopher; Oldfors, Anders 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) ↗
155. Case of late-onset Sandhoff disease due to a novel mutation in the HEXB gene. (August 2018) Authors: Sung, Angela R.; Moretti, Paolo; Shaibani, Aziz 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) ↗
156. Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging. (August 2021) Authors: Kikumoto, Mai; Nezu, Tomohisa; Shiga, Yuji; Motoda, Atsuko; Toko, Megumi; Kurashige, Takashi; Ueno, Hiroki; Takahashi, Tetsuya; Morino, Hiroyuki; Sone, Jun; Iwasaki, Yasushi; Sobue, Gen; Maruyama, Hirofumi Journal: Neurology Issue: Volume 7:Number 4(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
157. Cataglyphis meets Drosophila. (2nd January 2020) Authors: Wehner, Rüdiger Journal: Journal of neurogenetics Issue: Volume 34:Number 1(2020) Page Start: 184 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
158. CDKL5 variants: Improving our understanding of a rare neurologic disorder. (December 2017) Authors: Hector, Ralph D.; Kalscheuer, Vera M.; Hennig, Friederike; Leonard, Helen; Downs, Jenny; Clarke, Angus; Benke, Tim A.; Armstrong, Judith; Pineda, Mercedes; Bailey, Mark E.S.; Cobb, Stuart R. Journal: Neurology Issue: Volume 3:Number 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
159. Cell Adhesion in the Assembly of the Drosophila Eye. (December 2014) Authors: Bao, Sujin Journal: Journal of neurogenetics Issue: Volume 28:Number 3/4(2014) Page Start: 282 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
160. Cell-type-specific promoters for C. elegans glia. (1st October 2020) Authors: Fung, Wendy; Wexler, Leigh; Heiman, Maxwell G. Journal: Journal of neurogenetics Issue: Volume 34:Number 3/4(2020) Page Start: 335 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗