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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Intracerebral Hemorrhage
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Migraine and Cerebral White Matter Lesions
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A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
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Genetic Factors in Alzheimer's Disease
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Heritability of Carotid Artery Atherosclerotic Lesions
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Unusual Variants of Alexander's Disease
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Sensorineural Hearing Loss in Children
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
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Role of Cerebral Amyloid Angiopathy in Intracerebral Hemorrhage in Hypertensive Patients
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The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
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Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
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The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
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Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
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Recommended Standard of Cerebrospial Fluid Analysis in the Diagnosis of Multiple Sclerosis, A Consensus Statement
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Malignant Hyperthermia, Update on Susceptibility Testing
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A 10-Item Smell Identification Scale Related to Risk for Alzheimers Disease
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Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
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Phaeochromocytoma
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Update on Susacs Syndrome
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Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
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Unusual Presentation of Central Nervous System Cryptococcal Infection in an Immunocompetent Patient
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Diagnosis, Treatment, and Prognosis of Mycoplasma Pneumoniae Childhood Encephalitis: Systematic Review of 58 Cases
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Clinical Manifestations of Cerebral Amyloid Angiopathy-Related Inflammation
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Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
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Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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CADASIL: Cerebral Autosomal Subcortical Infarcts and Leukoecephalopathy
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
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The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
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Gene Transfer for Neurologic Disease
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Systemic Inflammatory Response Depends on Initial Stroke Severity but is Attenuated by Successful Thrombolysis
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Pathogenetic Mechanisms of Parkin in Parkinson's Disease
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White Matter Lesions, Congition, and Recurrent Hemorrhage in Lobar Intracerebral Hemorrhage
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The Occurence of Guillain-Barre Syndrome Within Families
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The Metabolic Syndrome, Inflammation, and Risk of Cognitive Decline
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Natural History of Nonketotic Hyperglycinemia in 65 Patients
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CJD--A Case of Mistaken Identity
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MR Spectroscopy in the Diagnosis of Cerebral Amyloid Angiopathy Presenting as a Brain Tumor
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Reversible Leukoencephalopathy Associated with Cerebral Amyloid Angiopathy
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Cognitive Functions in Survivors of Primary Central Nervous System Lymphoma
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