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Lucia Petrozzi

Showing results (1-10 of 36) with videos related to

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Bioscience Reports|May 9, 2007
Mitochondria and neurodegenerationLucia Petrozzi, Giulia Ricci, Noemi J Giglioli, et al.
Mutation Research|August 2, 2005
Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseasesFabio Coppedè, Chiara Armani, Damiana Della Bidia, et al.
Coronary Artery Disease|October 24, 2002
Elevated levels of oxidative DNA damage in patients with coronary artery diseaseNicoletta Botto, Serena Masetti, Lucia Petrozzi, et al.
Journal of the Neurological Sciences|October 2, 2010
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemiaSihem Souilem, Saber Chebel, Michelangelo Mancuso, et al.
Neuroscience Letters|October 1, 2013
Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of artLorenzo Kiferle, Daniele Orsucci, Michelangelo Mancuso, et al.
Neuroscience Letters|January 24, 2007
A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's diseaseFabio Coppedè, Michelangelo Mancuso, Annalisa Lo Gerfo, et al.
Neuroscience Letters|July 7, 2007
Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genesLorenzo Kiferle, Roberto Ceravolo, Lucia Petrozzi, et al.
Neuromuscular Disorders : NMD|June 2, 2012
Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatmentDaniele Orsucci, Chiara Pizzanelli, Greta Alì, et al.
CNS & Neurological Disorders Drug Targets|July 24, 2018
Amyotrophic Lateral Sclerosis and Oxidative Stress: A Double-Blind Therapeutic Trial After Curcumin SupplementationLucia Chico, Elena Caldarazzo Ienco, Costanza Bisordi, et al.
Biochemical and Biophysical Research Communications|February 6, 2007
MERRF syndrome without ragged-red fibers: the need for molecular diagnosisMichelangelo Mancuso, Lucia Petrozzi, Massimiliano Filosto, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Bioscience Reports|May 9, 2007
Mitochondria and neurodegenerationLucia Petrozzi, Giulia Ricci, Noemi J Giglioli, et al.
Mutation Research|August 2, 2005
Molecular implications of the human glutathione transferase A-4 gene (hGSTA4) polymorphisms in neurodegenerative diseasesFabio Coppedè, Chiara Armani, Damiana Della Bidia, et al.
Coronary Artery Disease|October 24, 2002
Elevated levels of oxidative DNA damage in patients with coronary artery diseaseNicoletta Botto, Serena Masetti, Lucia Petrozzi, et al.
Journal of the Neurological Sciences|October 2, 2010
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemiaSihem Souilem, Saber Chebel, Michelangelo Mancuso, et al.
Neuroscience Letters|October 1, 2013
Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: a case report and an update on the state of artLorenzo Kiferle, Daniele Orsucci, Michelangelo Mancuso, et al.
Neuroscience Letters|January 24, 2007
A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's diseaseFabio Coppedè, Michelangelo Mancuso, Annalisa Lo Gerfo, et al.
Neuroscience Letters|July 7, 2007
Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genesLorenzo Kiferle, Roberto Ceravolo, Lucia Petrozzi, et al.
Neuromuscular Disorders : NMD|June 2, 2012
Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatmentDaniele Orsucci, Chiara Pizzanelli, Greta Alì, et al.
CNS & Neurological Disorders Drug Targets|July 24, 2018
Amyotrophic Lateral Sclerosis and Oxidative Stress: A Double-Blind Therapeutic Trial After Curcumin SupplementationLucia Chico, Elena Caldarazzo Ienco, Costanza Bisordi, et al.
Biochemical and Biophysical Research Communications|February 6, 2007
MERRF syndrome without ragged-red fibers: the need for molecular diagnosisMichelangelo Mancuso, Lucia Petrozzi, Massimiliano Filosto, et al.
Pageof 4