Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
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A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021
A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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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
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Neurosyphilis
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Subacute Sclerosing Panencephalitis
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
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The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
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Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
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Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
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Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
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Neurological Presentation of Fabry's Disease in a 52 Year Old Man
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Niemann-Pick Disease Type C: Two Cases and an Update
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Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
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The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Niemann-Pick Disease Type C from Bench to Bedside
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Cytomegalovirus Encephalitis
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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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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
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HIV Encephalopathy and Dementia
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
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