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Showing articles 0 to 6 of 6 Filter Applied: lactic acidemia (Click to remove) Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 Showing articles 0 to 6 of 6