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Showing articles 0 to 10 of 10 Filter Applied: mitochondrial disease (Click to remove) Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Late-Onset Mitochondrial Myopathy Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995 Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995 Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction Ann Neurol 29:606-614, Mhiri,C.,et al, 1991 Showing articles 0 to 10 of 10