1. A population‐based study of scoliosis among males diagnosed with a dystrophinopathy identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet). Issue 2 (1st December 2021) Authors: Conway, Kristin M.; Gedlinske, Amber; Mathews, Katherine D.; Perlman, Seth; Johnson, Nicholas; Butterfield, Russell; Hung, Man; Bounsanga, Jerry; Matthews, Dennis; Oleszek, Joyce; Romitti, Paul A. Journal: Muscle & nerve Issue: Volume 65:Issue 2(2022) Page Start: 193 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional study. (12th July 2016) Authors: Johnson, Nicholas E.; Butterfield, Russell; Berggren, Kiera; Hung, Man; Chen, Wei; DiBella, Deanna; Dixon, Melissa; Hayes, Heather; Pucillo, Evan; Bounsanga, Jerry; Heatwole, Chad; Campbell, Craig Journal: Neurology Issue: Volume 87:Number 2(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Muscle at the junction: Where next generation sequencing is sending us. (26th March 2019) Authors: Johnson, Nicholas E.; Butterfield, Russell Journal: Neurology Issue: Volume 92:Number 13(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Rapid clinical diagnostic variant investigation of genomic patient sequencing data with iobio web tools. Issue 6 (23rd April 2018) Authors: Ward, Alistair; Karren, Mary A.; Di Sera, Tonya; Miller, Chase; Velinder, Matt; Qiao, Yi; Filloux, Francis M.; Ostrander, Betsy; Butterfield, Russell; Bonkowsky, Joshua L.; Dere, Willard; Marth, Gabor T. Journal: Journal of clinical and translational science Issue: Volume 1:Issue 6(2017) Page Start: 381 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial. Issue 10329 (12th March 2022) Authors: McDonald, Craig M; Marbán, Eduardo; Hendrix, Suzanne; Hogan, Nathaniel; Ruckdeschel Smith, Rachel; Eagle, Michelle; Finkel, Richard S; Tian, Cuixia; Janas, Joanne; Harmelink, Matthew M; Varadhachary, Arun S; Taylor, Michael D; Hor, Kan N; Mayer, Oscar H; Henricson, Erik K; Furlong, Pat; Ascheim, ... Journal: Lancet Issue: Volume 399:Issue 10329(2022) Page Start: 1049 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗