Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Central Nervous System Involvement in Whipple Disease
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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Sarcoidosis of the Nervous System, A Clinical Approach
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Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
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Neurologic Abnormalities of Lyme Disease
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Neurological Problems in Endocrine Diseases
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
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An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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Wernekinck Commissure Syndrome
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A Dizzy Architect
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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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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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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A 60-year-old woman with ataxia
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
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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 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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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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Progressive Cerebellar Ataxia and New-Onset Diabetes
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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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Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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The Autosomal Recessive Cerebellar Ataxias
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Epstein-Barr Virus Infections of the Nervous System
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005
Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003
Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001
Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997
Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997
Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997
Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997
A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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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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