Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
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Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
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Niemann-Pick Type C Disease
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Niemann-Pick Disease Type C
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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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A Triad of Tremor, Ataxia, and Cognitive Impairment
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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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 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
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Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
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Cognitive Delay in a 7-year-old Girl
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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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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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First Symptom in Sporadic Creutzfeldt-Jakob Disease
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Mitochondrial DNA Polymerase-y and Human Disease
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Clinical Manifestations of Sarin Nerve Gas Exposure
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Neurological Complications of Coeliac Disease
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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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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
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Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
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Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
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BSE Linked to New Variant of CJD in Humans
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Niemann-Pick Disease Type C from Bench to Bedside
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Opsoclonus
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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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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