Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
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Spastic Paraparesis after Anaesthesia
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Long-Term Postoperative Cognitive Dysfunction in the Elderly:ISPOCD1 Study
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Cognitive and Functional Competence after Anaesthesia in Patients Aged Over 60:General and Regional Anaesthesia
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Tuberous Sclerosis Complex:Clinical Features
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Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022
Sturge-Weber Syndrome
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The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022
CLOVES Syndrome
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Congenital Cytomegalovirus Infection
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Antibody-Mediated Encephalitis
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Primary Angiitis of the Central Nervous System
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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An 11-year-old Boy with Language Disorder and Epilepsy
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016
Sturge-Weber Syndrome
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Mystery Case: A Young Boy with Myoclonic Jerks
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Cognitive Delay in a 7-year-old Girl
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Sturge-Weber Syndrome
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
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Autoimmune encephalitis
BMJ 342:d1918, Irani, S.R.,et all, 2011
Huntingtons Disease
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Aicardi-Gouti�res Syndrome
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A 23-Year-Old Man With Seizures and Visual Deficit
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Overview of Phenylketonuria
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GAMT Deficiency: Features, Treatment, and Outcome in an Inborn Error of Creatine Synthesis
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Central Nervous System Injury Associated with Cardiac Surgery
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West Nile Virus Neuroinvasive Disease
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Agenesis of the Corpus Callosum:A United Kingdom Series of 56 Cases
JNNP 64:131-134, Taylor,M.&David,A.S., 1998
Atrial Fibrillation is an Independent Determinant of Low Cognitive Function
Stroke 29:1816-1820, Kilander,L.,et al, 1998
Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997
Bilirubin Metabolism and Kernicterus
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Clinicopath Conf
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Cognitive Impairment & Mortality in a Cohort of Elderly People
BMJ 312:608-611, Gale,C.R.,et al, 1996
Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996
Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
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Primary Brain Tumors:Review of Etiology Diagnosis and Treatment
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