Mitochondrial DNA and Disease
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994
Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987
A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Mitochondrial Respiratory-Chain Diseases
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Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996
Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996
Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
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Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
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Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
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