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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Natural History in Proximal Spinal Muscular Atrophy
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Sensory Testing in Human Immunodeficiency Virus Type 1-Infected Men
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Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Predominantly Sensory Neuropathy in Pts with AIDS & AIDS-Related Complex
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Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
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Neurologic Manifestations of AIDS
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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Neurodegenerative Disease of Infancy & Childhood
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Risdiplam in Presymptomatic Spinal Muscular Atrophy
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Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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