A Middle-Aged Man with Progressive Gait Abnormalities
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Mitochondrial DNA and Disease
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Clinicopath Conf
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Changes in the Basal Ganglia Following Cyanide Poisoning
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Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020
A 57-Year-Old Woman with Progressive Ataxia and Falls
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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When MRI is a Clue in Episodic Ataxia
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Recurrent Dysarthria and Ataxia in a Young Girl
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A Woman in Her 60s with Chronic Meningitis from Aspergillus
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A Case of Early-Onset Rapidly Progressive Dementia
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Subacute Sclerosing Panencephalitis
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The Thalamic Ataxia Syndrome
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023
A 67-YEar-Old Man with Multiple Intracranial Lesions
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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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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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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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Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
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Stridor in Multiple System Atrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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An Unusual Fundus Finding in a Teenage Girl
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