Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
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Neuro-Ophthalmic Manifestations of Lyme Disease
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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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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Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
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A 7-Year-Old Boy with Acute-Onset Altered Mental Status
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
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CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
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A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019
A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019
Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019
A 12-year-old girl with headache and change in mental status
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Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
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"Phacing" a New Cause of Carotid Artery Dissection
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017
The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
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Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
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Parry Romberg Syndrome: 7 Cases and Literature Review
AJNR 36:1355-1361, Wong, M.,et al, 2015
Extraintestinal Manifestations of Coeliac Disease
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Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
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Sturge-Weber Syndrome
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Mercury
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Inherited Metabolic Diseases of the Nervous System, Fabry Disease
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Transverse Myelitis Plus Syndrome and Acute Disseminated Encephalomyelitis Plus Syndrome
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The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
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Sturge-Weber Syndrome
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Clinical Characteristics of Pediatric-onset Neuro-Behcet Disease
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Neuroimaging in Cockayne Syndrome
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Lyme Neuroborreliosis: Manifestations of a Rapidly Emerging Zoonosis
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Aicardi-Gouti�res Syndrome
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Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
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Tuberous Sclerosis
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Acute Transverse Myelitis in Childhood: Center-Based Analysis of 47 Cases
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Practice Parameter: Treatment of Nervous System Lyme Disease (An Evidence-Based Review)
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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A Painful Hip as a Presentation of Guillain-Barre Syndrome in Children
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Optic Neuropathy in Children With Lyme Disease
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Dermatomyositis
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Characterization of Lyme Meningitis and Comparison with Viral Meningitis in Children
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Pain and the Guillain-Barre Syndrome in Children Under 6 Years
J Pediatr 134:773-776, Nguyen,D.K.,et al, 1999
Diversity in Presenting Manifestations of Systemic Lupus Erythematosus in Children
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
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