Linda Greensmith
Affiliations: | Sobell Department of Motor Neuroscience and Movement Disorders | UCL Institute of Neurology, Queen Square, London, England, United Kingdom |
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Ahmed M, Spicer C, Harley J, et al. (2023) Amplifying the Heat Shock Response Ameliorates ALS and FTD Pathology in Mouse and Human Models. Molecular Neurobiology |
Fisher EMC, Greensmith L, Malaspina A, et al. (2023) Opinion: more mouse models and more translation needed for ALS. Molecular Neurodegeneration. 18: 30 |
Bendotti C, Bonetto V, Pupillo E, et al. (2020) Focus on the heterogeneity of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-11 |
Gray AL, Annan L, Dick JRT, et al. (2020) Deterioration of muscle force and contractile characteristics are early pathological events in spinal and bulbar muscular atrophy mice. Disease Models & Mechanisms |
Fellows AD, Rhymes ER, Gibbs KL, et al. (2020) IGF1R regulates retrograde axonal transport of signalling endosomes in motor neurons. Embo Reports. e49129 |
Lombardi V, Bombaci A, Zampedri L, et al. (2019) Plasma pNfH levels differentiate SBMA from ALS. Journal of Neurology, Neurosurgery, and Psychiatry |
Klickovic U, Zampedri L, Sinclair CDJ, et al. (2019) Skeletal muscle MRI differentiates SBMA and ALS and correlates with disease severity. Neurology |
Tyzack GE, Luisier R, Taha DM, et al. (2019) Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis. Brain : a Journal of Neurology |
Clarke BE, Gil RS, Yip J, et al. (2019) Regional differences in the inflammatory and heat shock response in glia: implications for ALS. Cell Stress & Chaperones |
Malik B, Devine H, Patani R, et al. (2019) Gene expression analysis reveals early dysregulation of disease pathways and links Chmp7 to pathogenesis of spinal and bulbar muscular atrophy. Scientific Reports. 9: 3539 |