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MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options
Publication date: Available online 15 June 2015 Source:Molecular Genetics and Metabolism Author(s): Ayman W. El-Hattab , Adekunle M. Adesina , Jeremy Jones , Fernando Scaglia Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is one of the most frequent maternally inherited mitochondrial disorders. MELAS syndrome is a multi-organ disease with broad manifestations including stroke-like episodes, dementia, epilepsy, lactic acidemia, myopathy, recurrent headaches, hearing impairment, diabetes, and short stature. The most common mutation associated with MELAS syndrome is the m.3243A&a...
Source: Molecular Genetics and Metabolism - June 27, 2015 Category: Genetics & Stem Cells Source Type: research
