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Ageing Research Reviews|November 16, 2023
Genomic and transcriptomic advances in amyotrophic lateral sclerosisMafalda Rizzuti, Luca Sali, Valentina Melzi, et al.
Journal of Cellular and Molecular Medicine|July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophyDelia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.
European Journal of Human Genetics : EJHG|December 23, 2011
The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairmentDario Ronchi, Monica Sciacco, Andreina Bordoni, et al.
Biochemical and Biophysical Research Communications|August 9, 2011
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutationDario Ronchi, Andreina Bordoni, Alessandra Cosi, et al.
Journal of the Neurological Sciences|June 22, 2011
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegiaDario Ronchi, Elisa Fassone, Andreina Bordoni, et al.
Progress in Neurobiology|April 27, 2020
miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosisAlessia Loffreda, Monica Nizzardo, Alessandro Arosio, et al.
Brain : a Journal of Neurology|October 9, 2012
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletionsDario Ronchi, Caterina Garone, Andreina Bordoni, et al.
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