Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
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Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
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A 10-year-old boy with Bilateral Vision Loss
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Mouse Infestation Likely Source of Lymphocytic Choriomeningitis in Teen
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Molybdenum Cofactor Deficiency
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The Limbic-Girdle Muscular Dystrophies
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Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
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The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
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Heterogeneity of Coenzyme Q10 Deficiency
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
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Magnetic Resonance Imaging of Biceps Femoris Muscles in Benign Acute Childhood Myositis
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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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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Mitochondrial DNA Polymerase-y and Human Disease
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Sensorineural Hearing Loss in Children
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Adrenoleukodystrophy
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Dermatomyositis
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Benign Acute Childhood Myositis, Laboratory and Clinical Features
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Headaches in Children Younger than 7 Years of Age
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A Clinical Study of Noonan Syndrome
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Clinical Uses of Intravenous Immunoglobulins
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Cysticercosis-Review of 230 Patients
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Childhood Dermatomyositis:Factors Predicting Functional Outcome and Development of Dystrophic Calcification
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Benign Acute Childhood Myositis
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Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Clinical Features, Diagnosis and Management of Klinefelter Syndrome
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Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
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A Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023
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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An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022
The Phenotypic Continuum of ATP1A3-Related Disorders
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Acute Flaccid Myelitis: Cause, Diagnosis, and Management
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A Teenager with Shortness of Breath and Difficulty Walking
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Neurologic Involvement in Children and Adolescents Hospitalized in the United States for Covid-19 or Multisystem Inflammatory Syndrome
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021
Determination of Brain Death
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Hopkins Syndrome
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Childhood Multisystem Inflammatory Syndrome
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Determination of Brain Death/Death by Neurologic Criteria
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Radiologically Isolated Syndrome: A Review for Neuroradiologists
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