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MELAS
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Precipitating Factors in Pituitary Apoplexy
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Twelve Cases of Pituitary Apoplexy
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Malignant Tumors in the Pituitary Gland
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Neuro-Ophthalmologic Signs of AIDS:50 patients
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Neurological Problems in Endocrine Diseases
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Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
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The Tolosa-Hunt Syndrome
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Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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Orbital Apex Syndrome
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A Child with Arthrogryposis
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Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018
A Child with Delayed Motor Milestones and Ptosis
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Myasthenia Gravis
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Ptosis, Erythema, and Rapidly Decreasing Vision
JAMA 309:2382-2383, Zanation, A.,et al, 2013
Central Nervous System Involvement in Whipple Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Cytomegalovirus Ventriculoencephalitis Presenting as a Wernicke's Encephalopathy-like Sydrome
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Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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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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Oculo-Facial-Skeletal Myorhythmia in Whipple Disease:Treatment with Ceftriazone
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Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990
Neurologic Sequelae of Domoic Acid Intoxication Due to the Ingestion of Contaminated Mussels
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Orbital Myositis and Giant Cell Myocarditis
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Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Clinical Signs in the Wernicke-Korsakoff Complex:A Retrospective Analysis of 131 Cases Diagnosed at Necropsy
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985
Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984
Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983
Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981
Nervous System Toxicity of Chemo Agents
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Neurologic Abnormalities of Lyme Disease
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