A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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Central Nervous System Involvement in Whipple Disease
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Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
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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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Neurotoxicity of Commonly Used Antineoplastic Agents
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022
Adult-Onset Niemann-Pick Disease Type C Masquerading As Spinocerebellar Ataxias
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Cerebellar Ataxia and Hearing Impairment
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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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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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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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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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
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Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
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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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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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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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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990
Progressive Rubella Panencephalitis
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Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
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