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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Ears of the Lynx Magnetic Resonance Imaging Sign
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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A 60-year-old man with arm weakness and numbness
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Clinical Reasoning: A Teenager with Left Arm Weakness
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A 42-year-old man with unilateral leg weakness
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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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 Neonate with Micrognathia and Hypotonia
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
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Dopamine-Responsive Dystonia
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Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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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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Can We Prevent Cerebral Palsy?
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Familial Amyotrophic Lateral Sclerosis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Amyotrophic Lateral Sclerosis
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Distal Hereditary Upper Limb Muscular Atrophy
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
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Hereditary Form of Parkinsonism-Dementia
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Facial Nerve is Liable to Pressure Palsy
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
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