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Browsing by Author Carrozzo, Rosalba

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Issue DateTitleAuthor(s)
2009Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNADi Fabio, Roberto; Santorelli, Filippo M.; Nola, Giuseppe; Cricchi, Federica; Masi, Roberto; Ingrosso, Angelo; Fattori, Fabiana; Carrozzo, Rosalba; Vanacore, Nicola; Pierelli, Francesco; Ralli, Giovanni; Casali, Carlo
2003Leigh syndrome associated mutations induce apoptotic proneness by yelding hyperpolarization of mitochondriaMatarrese, Paola; Carrozzo, Rosalba; Santorelli, Filippo M.; Rizza, Teresa; Ascione, Barbara; Malorni, Walter
2004Maternally-inherited Leigh syndrome-related mutations bolster mitochondrial-mediated apoptosisCarrozzo, Rosalba; Rizza, Teresa; Stringaro, Annarita; Pierini, Roberta; Mormone, Elisabetta; Santorelli, Filippo M.; Malorni, Walter; Matarrese, Paola
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