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Gene|June 1, 2005
Disorders of nuclear-mitochondrial intergenomic signalingAntonella Spinazzola, Massimo ZevianiAdvances in Experimental Medicine and Biology|March 13, 2010
Mitochondrial diseases: a cross-talk between mitochondrial and nuclear genomesAntonella Spinazzola, Massimo ZevianiBioscience Reports|May 19, 2007
Disorders of nuclear-mitochondrial intergenomic communicationAntonella Spinazzola, Massimo ZevianiCurrent Neurology and Neuroscience Reports|August 14, 2003
Mitochondrial disordersMassimo Zeviani, Antonella SpinazzolaCurrent Opinion in Genetics & Development|June 6, 2003
Nuclear genes in mitochondrial disordersMassimo Zeviani, Antonella Spinazzola, Valerio CarelliNeuromuscular Disorders : NMD|November 27, 2004
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G-->A mitochondrial DNA mutationAntonella Spinazzola, Franco Carrara, Marina Mora, et al.Neuromuscular Disorders : NMD|February 12, 2008
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and ItaliansAntonella Spinazzola, Valeria Massa, Michio Hirano, et al.Human Molecular Genetics|September 27, 2008
Early-onset liver mtDNA depletion and late-onset proteinuric nephropathy in Mpv17 knockout miceCarlo Viscomi, Antonella Spinazzola, Marco Maggioni, et al.Nature Genetics|April 4, 2006
Systematic identification of human mitochondrial disease genes through integrative genomicsSarah Calvo, Mohit Jain, Xiaohui Xie, et al.Pageof 31