11. Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies. (2nd January 2018) Authors: Burnor, Elisabeth; Yang, Li; Zhou, Hao; Patterson, Kristina R.; Quinn, Colin; Reilly, Mary M.; Rossor, Alexander M.; Scherer, Steven S.; Lancaster, Eric Journal: Neurology Issue: Volume 90:Number 1(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Plasma neurofilament heavy chain is not a useful biomarker in Charcot–Marie–Tooth disease. Issue 6 (27th April 2016) Authors: Rossor, Alexander M.; Liu, Ching‐Hua; Petzold, Axel; Malaspina, Andreas; Laura, Matilde; Greensmith, Linda; Reilly, Mary M. Journal: Muscle & nerve Issue: Volume 53:Issue 6(2016) Page Start: 972 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Plasma neurofilament light chain concentration in the inherited peripheral neuropathies. (6th February 2018) Authors: Sandelius, Åsa; Zetterberg, Henrik; Blennow, Kaj; Adiutori, Rocco; Malaspina, Andrea; Laura, Matilde; Reilly, Mary M.; Rossor, Alexander M. Journal: Neurology Issue: Volume 90:Number 6(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Recent advances in the genetic neuropathies. Issue 5 (October 2016) Authors: Rossor, Alexander M.; Tomaselli, Pedro J.; Reilly, Mary M. Journal: Current opinion in neurology Issue: Volume 29:Issue 5(2016:Oct.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy. (10th June 2015) Authors: Rossor, Alexander M.; Oates, Emily C.; Salter, Hannah K.; Liu, Yang; Murphy, Sinead M.; Schule, Rebecca; Gonzales, Michael A.; Scoto, Mariacristina; Phadke, Rahul; Sewry, Caroline A.; Houlden, Henry; Jordanova, Albena; Tournev, Iyailo; Chamova, Teodora; Litvinenko, Ivan; Zuchner, Stephan; Herrman... Journal: Brain Issue: Volume 138:Part 11(2015:Nov.) Page Start: e392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Semi‐dominant mutations in MFN2‐related neuropathy and implications for genetic counselling. Issue 1 (March 2016) Authors: Tomaselli, Pedro J.; Rossor, Alexander M.; Polke, James M.; Poh, Roy; Blake, Julian; Reilly, Mary M. Journal: Journal of the peripheral nervous system Issue: Volume 21:Issue 1(2016) Page Start: 52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Severe cognitive impairment in a patient with CMT2A. Issue 2 (26th March 2018) Authors: Tomaselli, Pedro J.; Kapoor, Mahima; Cortese, Andrea; Polke, James M.; Rossor, Alexander M.; Reilly, Mary M. Journal: Journal of the peripheral nervous system Issue: Volume 23:Issue 2(2018) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN. (26th February 2019) Authors: Rossor, Alexander M.; Jaunmuktane, Zane; Rossor, Martin N.; Hoti, Glen; Reilly, Mary M. Journal: Neurology Issue: Volume 92:Number 9(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A. Issue 1 (12th December 2019) Authors: Wang, Hongge; Davison, Matthew; Wang, Kathryn; Xia, Tai‐He; Kramer, Martin; Call, Katherine; Luo, Jun; Wu, Xingyao; Zuccarino, Riccardo; Bacon, Chelsea; Bai, Yunhong; Moran, John J.; Gutmann, Laurie; Feely, Shawna M. E.; Grider, Tiffany; Rossor, Alexander M.; Reilly, Mary M.; Svaren, John; Shy, M... Journal: Annals of clinical and translational neurology Issue: Volume 7:Issue 1(2020) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗