The Phenotypic Continuum of ATP1A3-Related Disorders
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Dizzy Architect
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
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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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Rhombencephalitis A Series of 97 Patients
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
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Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Mitochondrial DNA and Disease
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Angelman Syndrome: Clinical Profile
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Self-Limited Granulomatous Angiitis of the Cerebellum
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Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
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Clinicopathological Conference, Powasan Virus Encephalitis
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The Spectrum of Fragile X Disorders
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
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