A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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Cognitive Delay in a 7-year-old Girl
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Niemann-Pick Type C Disease
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023
An 8-Year-Old with Acute Onset Ataxia
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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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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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
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Complex Ataxia
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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019
When MRI is a Clue in Episodic Ataxia
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018
Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
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An Unusual Fundus Finding in a Teenage Girl
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017
Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017
A 27-year-old man with Acute-Onset 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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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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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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Reversible Cognitive Decline Diagnosed on Ear Examination
BMJ 352:e1215, Ellis, R.J.B.,et al, 2016
Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Extraintestinal Manifestations of Coeliac Disease
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014
Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014
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, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lead
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Cerebellitis (Acute Ataxia of Childhood)
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
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Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
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Subacute Sclerosing Panencephalitis
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Central Nervous System Involvement in Whipple Disease
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Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
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