Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986
Neurotoxicity of Commonly Used Antineoplastic Agents
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Rabies
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Mitochondrial DNA Polymerase-y and Human Disease
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Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996
Mitochondrial DNA and Disease
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
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Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Diagnostic Tests for Choreoacanthocytosis
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991
Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987
The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986
Neurologic Dysfunction in the Idiopathic Hypereosinophilic Syndrome
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
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Clin. Path. Conference
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981
Juvenile Metachromatic Leukodystrophy
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Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
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Central Nervous System Toxicity Associated With Metronidazole Therapy
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979
Late Adult-onset Metachromatic Leukodystrophy
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Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978
Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973
Multiple Sclerosis Associated with Defects in Neuromuscular Transmission
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Genetic Counseling in Retinitis Pigmentosa
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Central Nervous System Manifestations of Periarteritis Nodosa
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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
Behcets Syndrome
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
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Neonatal Seizures
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Posterior Reversible Encephalopathy Syndrome
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Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Neurological Events Reported after COVID-19 Vaccines: An Analysis of Vaccine Adverse Event Reporting System
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