Niemann-Pick Type C Disease
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A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022
Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022
A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021
Alzheimers Disease
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017
Huntington Disease: Clinical Features and Diagnosis
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Cerebral Amyloid Angiopathy
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009
MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
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Neuroimaging Findings in Human Prion Disease
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
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Migraine and Cerebral White Matter Lesions
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003
A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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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
Altered Brain Activation in Cognitively Intact Individuals at High Risk for Alzheimer's Disease
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997
X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997
Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Wilson Disease
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Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026
Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026
Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
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Infantile Epileptic Spasms Syndrome (West Syndrome)
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Neurosyphilis
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Niemann-Pick Disease Type C
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Vitamin B12 Deficiency:NICE Guideline Summary
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Primary Central Nervous System Vasculitis
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Genome Sequencing in the NICU and PICU is Here to Stay
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Revised Criteria for Diagnosis and Staging of Alzheimers Disease: Alzheimers Association Workgroup
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023
Neonatal Seizures
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Current and Emerging Issues in Wilsons Disease
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