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Bioscience Reports
|
May 9, 2007
Mitochondria and neurodegeneration
Lucia 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 diseases
Fabio 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 disease
Nicoletta 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 hyperCKemia
Sihem 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 art
Lorenzo 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 disease
Fabio 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 genes
Lorenzo Kiferle, Roberto Ceravolo, Lucia Petrozzi, et al.
Neuromuscular Disorders : NMD
|
June 2, 2012
Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatment
Daniele 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 Supplementation
Lucia 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 diagnosis
Michelangelo Mancuso, Lucia Petrozzi, Massimiliano Filosto, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
Bioscience Reports
|
May 9, 2007
Mitochondria and neurodegeneration
Lucia 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 diseases
Fabio 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 disease
Nicoletta 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 hyperCKemia
Sihem 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 art
Lorenzo 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 disease
Fabio 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 genes
Lorenzo Kiferle, Roberto Ceravolo, Lucia Petrozzi, et al.
Neuromuscular Disorders : NMD
|
June 2, 2012
Nerve, muscle and heart acute toxicity following oxaliplatin and capecitabine treatment
Daniele 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 Supplementation
Lucia 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 diagnosis
Michelangelo Mancuso, Lucia Petrozzi, Massimiliano Filosto, et al.
Page
of 4