Mitochondria in Sporadic Amyotrophic Lateral Sclerosis - Swerdlow, Russell H.; Parks, Janice K.; Cassarino, David S.; Trimmer, Patricia A.; Miller, Scott W.; Maguire, David J.; Sheehan, Jason P.; Maguire, Robyn S.; Pattee, Gary; Juel, Vern C.; Phillips, Lawrence H.; Tuttle, Jeremy B.; et al. (Experimental neurology, 1998)
Keywords: 1-Methyl-4-phenylpyridinium - metabolism; ALS; amyotrophic lateral sclerosis; Amyotrophic Lateral Sclerosis - genetics; Amyotrophic Lateral Sclerosis - pathology; Animals; Biological and medical sciences; calcium; Calcium - metabolism; Cell Line; cybrids; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; DNA; DNA, Mitochondrial - genetics; DNA, Mitochondrial - metabolism; Electron Transport - genetics; Electron Transport - physiology; Female; Free Radical Scavengers - metabolism; Humans; Hybrid Cells; Male; Medical sciences; Mice; Microscopy, Electron; Middle Aged; mitochondria; Mitochondria - metabolism; Mitochondria - physiology; Mitochondria - ultrastructure; Mutation - genetics; Neurology; oxidative; calcium; DNA; mitochondria; ALS; oxidative; amyotrophic lateral sclerosis; cybrids; Human; Nervous system diseases; Sporadic; Pathogenesis; Central nervous system disease; Amyotrophic lateral sclerosis; Degenerative disease; Mitochondrial DNA; Mutation; Spinal cord disease; Mitochondrial disorder