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Parkinsonism & Related Disorders|April 20, 2006
Anticipation of onset age in familial Parkinson's disease without SCA gene mutationsYue Huang, Michael Hayes, Antony J Harding, et al.BMJ Open|October 4, 2016
Identification and outcomes of clinical phenotypes in amyotrophic lateral sclerosis/motor neuron disease: Australian National Motor Neuron Disease observational cohortPaul Talman, Thi Duong, Steve Vucic, et al.Journal of Neurochemistry|September 2, 2005
Differential effects of human neuromelanin and synthetic dopamine melanin on neuronal and glial cellsJie Li, Carsten Scheller, Eleni Koutsilieri, et al.Trials|January 6, 2025
Polysomnographic titration of non-invasive ventilation in motor neurone disease (3TLA): study protocol for a randomised controlled trialDavid J Berlowitz, Dominic Rowe, Mark E Howard, et al.Stem Cell Research|February 2, 2020
The mRNA-based reprogramming of fibroblasts from a SOD1E101G familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007Rachelle Balez, Tracey Berg, Monique Bax, et al.Communications Medicine|January 27, 2022
Pathological manifestation of human endogenous retrovirus K in frontotemporal dementiaKatherine Phan, Ying He, YuHong Fu, et al.Neuro-Degenerative Diseases|November 14, 2017
Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral SclerosisJennifer A Fifita, Katharine Y Zhang, Jasmin Galper, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 30, 2021
MiNDAUS partnership: a roadmap for the cure and management of motor Neurone diseaseSteve Vucic, Naomi Wray, Anjali Henders, et al.BMJ Open|June 18, 2026
Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profileAnjali K Henders, Laura Ziser, Fleur C Garton, et al.Pageof 2