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11. Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice. (28th November 2017)

12. Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. Issue 5 (May 2018)

13. SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed. Issue 4 (7th October 2021)

14. Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment bias. Issue 3 (30th September 2018)