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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
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Clinicopath Conf, Infantile Krabbe Disease
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Metabolic Disease and Stroke: MELAS
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Unusual Variants of Alexander's Disease
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Complex Ataxia
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
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Cerebellar Ataxia and Hearing Impairment
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Polycythemia Vera Presenting with Ischemic Strokes in Multiple Arterial Territories
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The Autosomal Recessive Cerebellar Ataxias
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An unusual cause of stroke and hypoxia
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Personalized Approaches to Clopidogrel Therapy: Are We There Yet?
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Neurologic Manifestations of von Hippel-Lindau Disease
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Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord
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Fragile X Premutation With Atypical Symptoms at Onset
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
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New Strategy for Prenatal Diagnosis of X-Linked Disorders
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Motor Changes in Presymptomatic Huntington Disease Gene Carriers
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The Inherited Ataxias and the New Genetics
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Trinucleotide Repeat Expansion in Neurological Disease
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