Friedreich Ataxia
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Cardiac Dysfunction in Neuromuscular Diseases
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Genetic Counseling in Retinitis Pigmentosa
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Cerebellar Ataxia in Children
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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The Autosomal Recessive Cerebellar Ataxias
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Genetic Testing in Spinocerebellar Ataxias
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Molecular Basis of the Neurodegenerative Disorders
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
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The Inherited Ataxias and the New Genetics
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Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
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Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
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Physostigmine in Familial Ataxias
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Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
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A Case of Cerebellar Ataxia, with a Discussion of Classification
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Hereditary Ataxias
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