Niemann-Pick Type C Disease
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
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Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
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CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
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An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
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Antibody-Mediated Encephalitis
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Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Neuroimaging Changes in Menkes Disease, Part 1
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Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
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Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
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Current Concept of Neuromyelitis Optica (NMO) and NMO Spectrum Disorders
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Brain Abnormalities in Neuromyelitis Optica Spectrum Disorder
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Late onset autism and anti-NMDA-receptor encephalitis
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Encephalitis Associated with Glutamic Acid Decarboxylase Autoantibodies in a Child A Treatable Condition?
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Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
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Huntingtons Disease
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A 23-Year-Old Man With Seizures and Visual Deficit
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Spinal Muscular Atrophy
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Recessive Ataxia With Ocular Apraxia
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Mucolipidosis Type IV; Characteristic MRI Findings
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Zorevunersen in Children and Adolescents with Dravet Syndrome
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Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
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A 5-Year-Old Boy with Subacute and Refractory Myoclonus
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
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Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
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Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
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Neuroimaging Features of Biotinidase Deficiency
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A 17-Year-Old Girl with Progressive Cognitive Impairment
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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A 6-Year-Old Girl with Progressive Toe Walking
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An 8-Year-Old with Acute Onset Ataxia
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
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The Phenotypic Continuum of ATP1A3-Related Disorders
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