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Spinal Muscular Atrophy
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Clinicopath Conf
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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Progressive Pontobulbar Palsy With Deafness
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Familial Occurrence of Meralgia Paresthetica
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Bilateral Hearing Loss and Constricted Visual Fields
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Amyotrophic Lateral Sclerosis
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 53-year-old Woman with Lower Extremity Paresthesias
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Clinical Reasoning: A Teenager with Left Arm 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 10-year-old boy with Bilateral Vision Loss
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A Neonate with Micrognathia and Hypotonia
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Hydrocephalus in Children
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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A Young Man with Progressive Vision and Hearing Loss
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Neurological Management of Von Hippel-Lindau Disease
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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The Limbic-Girdle Muscular Dystrophies
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The Autosomal Recessive Cerebellar Ataxias
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Spinal Muscular Atrophy A Timely Review
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
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Neurofibromatosis Type 2
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Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Neurologic Manifestations of von Hippel-Lindau Disease
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