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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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A Child with Delayed Motor Milestones and Ptosis
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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The Autosomal Recessive Cerebellar Ataxias
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An unusual cause of stroke and hypoxia
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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The Tuberous Sclerosis Complex
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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A 9-Year-Old Girl with CNS Immune Dysregulation
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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