Telemedicine in Neurology
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Transition to Adult Care for Children with Chronic Neurological Disorders
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Mitochondrial DNA and Disease
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Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
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Genetic Counseling in Retinitis Pigmentosa
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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A 23-Year-Old Man With Seizures and Visual Deficit
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Clinical Uses of Intravenous Immunoglobulins
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Explanation & Management of Neurological Disability
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Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
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Neurological Problems in Endocrine Diseases
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Neurocutaneous Disease
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Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
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A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
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A 59-Year-Old Man with Acute-Onset Encephalopathy and Aphasia
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A 5-Year-Old Boy with Subacute and Refractory Myoclonus
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Melas Syndrome
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024
A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
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Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024
Vascular Malformations of the Central Nervous System
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
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Sturge-Weber Syndrome
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
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Chronic Meningitis
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Case Report: Anti-NMDA Receptor Encephalitis with Bilateral Hearing Loss as the Initial Symptom
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Clinicopathologic Conference, Borrelia Miyamotoi Infection
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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Childhood Primary Angiitis of the Central Nervous System
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Clinical Reasoning: A 66-year-old Woman with Seizures and Progressive Right-Sided Weakness
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Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
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Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018
FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Cerebellar Ataxia and Hearing Impairment
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Primary Angiitis of the Central Nervous System
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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