Phosphorylase Deficiency
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McArdle's Disease in the 1980s
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Pernicious Anaemia
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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Clinopathologic Conference, Celiac Disease
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Challenges in the Identification of Cobalamin-Deficiency Polyneuropathy
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Practice Parameter: Diagnosis of Dementia (an Evidence-Based Review)
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Presenting Features and Value of Diagnostic Procedures in Leptomeningeal Metastases
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Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Neurologic Aspects of Cobalamin Deficiency
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Retinitis Pigmentosa
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Acid Maltase Deficiency
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Primary Central Nervous System Lymphoma:Clinical Features, Diagnosis, and Extent of Disease Evaluation
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Updates on Sturge-Weber Syndrome
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Sturge-Weber Syndrome
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Paraneoplastic Myeloneuropathies
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021
Clinicopathologic Conference, Normal Pressure Hydrocephalus
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Congenital Cytomegalovirus Infection
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Duchenne Muscular Dystrophy
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"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
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Muscular Dystrophies
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Imaging Features (CT, MRI, MRS, PET/CT) of Primary Central Nervous System Lymphoma in Immunocompetent Patients
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Neurodegeneration with Brain Iron Accumulation
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Antibody-Mediated Encephalitis
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Diagnosis and Management of the Antiphospholipid Syndrome
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Spontaneous Subarachnoid Haemorrhage
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Primary Angiitis of the Central Nervous System
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Overview of IgG4-related Disease
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Huntington Disease: Clinical Features and Diagnosis
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Myasthenia Gravis
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Kleine-Levin Syndrome in 120 Patients: Differential Diagnosis and Long Episodes
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Inflammatory Muscle Diseases
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Prevalence of Amyloid PET Positivity in Dementia Syndromes
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Diagnostic Criteria for IgG4-Related Ophthalmic Disease
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Diagnosis and Management of Marchiafava-Bignami Disease: A Review of CT/MRI Confirmed Cases
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
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Copper Deficiency Clinical Case Conference: In Defense of Checklists
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IgG4-Related Hypertrophic Pachymeningitis
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
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The Limbic-Girdle Muscular Dystrophies
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A Systematic Approach to the Diagnosis of Suspected Central Nervous System Lymphoma
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