Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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A 23-Year-Old Man With Seizures and Visual Deficit
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Spinal Muscular Atrophy
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Amyotrophic Lateral Sclerosis
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Alzheimer's Disease and Parkinson's Disease
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Ion Channel Diseases:Episodic Disorders of the Nervous System
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998
Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Progress in Tuberous Sclerosis
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Anderson-Fabry Disease
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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