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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Spinal Muscular Atrophy
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Genetics of Cluster Headache Takes a Leap
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Huntington Disease: Clinical Features and Diagnosis
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
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Diagnosis and New Treatments in Muscular Dystrophies
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Recessive Ataxia With Ocular Apraxia
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Familial Occurrence of Cluster Headache
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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X-Linked Pure Familial Spastic Paraparesis
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Cerebral Involvement in McLeod Syndrome
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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