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Intracellular to Interorgan Mitochondrial Communication in Striated Muscle in Health and Disease.
Endocr Rev. 2023 Jul 11;44(4):668-692. doi: 10.1210/endrev/bnad004.
Endocr Rev. 2023.
PMID: 36725366
Free PMC article.
Review.
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy.
Verrigni D, Di Nottia M, Ardissone A, Baruffini E, Nasca A, Legati A, Bellacchio E, Fagiolari G, Martinelli D, Fusco L, Battaglia D, Trani G, Versienti G, Marchet S, Torraco A, Rizza T, Verardo M, D'Amico A, Diodato D, Moroni I, Lamperti C, Petrini S, Moggio M, Goffrini P, Ghezzi D, Carrozzo R, Bertini E.
Verrigni D, et al. Among authors: trani g.
Hum Mutat. 2019 May;40(5):601-618. doi: 10.1002/humu.23729. Epub 2019 Mar 9.
Hum Mutat. 2019.
PMID: 30801875
Free article.
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A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly.
Di Nottia M, Marchese M, Verrigni D, Mutti CD, Torraco A, Oliva R, Fernandez-Vizarra E, Morani F, Trani G, Rizza T, Ghezzi D, Ardissone A, Nesti C, Vasco G, Zeviani M, Minczuk M, Bertini E, Santorelli FM, Carrozzo R.
Di Nottia M, et al. Among authors: trani g.
Neurobiol Dis. 2020 Jul;141:104880. doi: 10.1016/j.nbd.2020.104880. Epub 2020 Apr 25.
Neurobiol Dis. 2020.
PMID: 32344152
Free article.
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