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A Child with Delayed Motor Milestones and Ptosis
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Mitochondrial DNA Polymerase-y and Human Disease
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Erroneous Diagnosis Corrected After 28 Years
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Mitochondrial DNA and Disease
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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
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Ophthalmologic Manifestations in MELAS Syndrome
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Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
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Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
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External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
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Progressive Supranuclear Palsy-Case Study
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Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
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Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
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A Man with Rapidly Progressive Weakness and Respiratory Failure
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Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
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A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
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Pharyngeal-Cervical-Brachial Variant of Guillain-Barr� Syndrome
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Mitochondrial Respiratory-Chain Diseases
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Difference in Distribution of Muscle Weakness Between Myasthenia Gravis and the Lambert-Eaton Myasthenic Syndrome
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