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Title: α-Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation. Author: Takei Y, Oguchi K, Koshihara H, Hineno A, Nakamura A, Ohara S. Journal: Hum Pathol; 2013 Jun; 44(6):1171-6. PubMed ID: 23352207. Abstract: Immunohistochemical studies were performed on postmortem brain and spinal cord from a patient with familial amyotrophic lateral sclerosis characterized by a C111Y mutation in the Cu/Zn superoxide dismutase gene. Clinically, the patient presented with classical amyotrophic lateral sclerosis and died of respiratory failure at age 53 years without ventilator dependence, 4 years after the onset. Pathologically, loss of motor neurons was more extensive than upper motor neurons. Lower motor neurons developed massive intracellular cytoplasmic neuronal inclusions, which were immunoreactive for Cu/Zn superoxide dismutase and phosphorylated α-synuclein, often colocalized. The inclusions were TAR DNA-binding protein 43 negative. The clinicopathologic significance of coaggregation of α-synuclein and Cu/Zn superoxide dismutase protein, a novel finding in neurodegenerative disorders, needs further investigation.[Abstract] [Full Text] [Related] [New Search]