971. White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutations. (February 2016) Authors: Ameur, Fatima; Colliot, Olivier; Caroppo, Paola; Ströer, Sebastian; Dormont, Didier; Brice, Alexis; Azuar, Carole; Dubois, Bruno; Le Ber, Isabelle; Bertrand, Anne Journal: Neurology Issue: Volume 2:Number 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
972. Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington Disease. (February 2021) Authors: Amador, Maria del Mar; Gargiulo, Marcela; Boucher, Christilla; Herson, Ariane; Staraci, Stéphanie; Salachas, François; Clot, Fabienne; Cazeneuve, Cécile; Le Ber, Isabelle; Durr, Alexandra 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) ↗
973. Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease. (October 2017) Authors: Ruiz-Martínez, Javier; Azcona, Luis J.; Bergareche, Alberto; Martí-Massó, Jose F.; Paisán-Ruiz, Coro 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) ↗
974. Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome. (April 2018) Authors: Alrohaif, Hadil; Töpf, Ana; Evangelista, Teresinha; Lek, Monkol; McArthur, Daniel; Lochmüller, Hanns Journal: Neurology Issue: Volume 4:Number 2(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
975. Whole-exome sequencing in neurologic practice: Reducing the diagnostic odyssey. (December 2015) Authors: Johnson, Nicholas E. Journal: Neurology Issue: Volume 1:Number 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
976. Whole-exome sequencing to disentangle the complex genetics of hippocampal sclerosis–temporal lobe epilepsy. (June 2018) Authors: Striano, Pasquale; Nobile, Carlo 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) ↗
977. Whole-Genome and Long-Read Sequencing Identify a Novel Mechanism in RFC1 Resulting in CANVAS Syndrome. (1st December 2022) Authors: King, Katherine Abell; Wegner, Daniel J.; Bucelli, Robert C.; Shapiro, Jessica; Paul, Alexander J.; Dickson, Patricia I.; Wambach, Jennifer A. Journal: Neurology Issue: Volume 8:Number 6(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
978. Wiring dendrites in layers and columns. (2nd April 2016) Authors: Luo, Jiangnan; McQueen, Philip G.; Shi, Bo; Lee, Chi-Hon; Ting, Chun-Yuan Journal: Journal of neurogenetics Issue: Volume 30:Number 2(2016) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
979. Women in science: a daughter's perspective. (3rd July 2021) Authors: Sokolowski, H. Moriah Journal: Journal of neurogenetics Issue: Volume 35:Number 3(2021) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
980. Women in science: a son's perspective. (3rd July 2021) Authors: Sokolowski, Dustin J. Journal: Journal of neurogenetics Issue: Volume 35:Number 3(2021) Page Start: 104 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗