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You searched for: Author/Creator Jokela, Manu

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1. An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy. (2nd April 2019)

2. CHCHD10 mutations and motor neuron disease: the distribution in Finnish patients. Issue 3 (3rd November 2016)

3. Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy. Issue 4 (7th March 2022)

7. Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial. Issue 10 (October 2021)