A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024
A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024
Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023
Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020
Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Immune Checkpoint Inhibitor-Related Myositis and Myocarditis in Patients with Cancer
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016
Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
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Heterogeneity of Coenzyme Q10 Deficiency
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Dropped Head Syndrome: Report of Three Cases During Treatment with a Mek Inhibitor
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The Floppy Infant: Evaluation of Hypotonia
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A Forearm Exercise Screening Test for Mitochondrial Myopathy
Neurol 58:1533-1538, Jensen,T.D.,et al, 2002
Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998
Bent Spine Syndrome
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Late-Onset Mitochondrial Myopathy
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Mitochondrial DNA and Disease
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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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
Sudden Onset of Profound Weakness in a Toddler
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Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
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Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992
Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
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Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
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Muscle Carnitine Deficiency in Patients Using Valproic Acid
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Adult Phosphorylase b Kinase Deficiency
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Mitochondrial Myopathies, Mechanisms Now Better Understood
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
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MELAS Syndrome Involving a Mother & Two Children
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Unusual Neurotoxicity Associated with Amiodarone Therapy
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