Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Genetic Aspects of Alzheimer Disease
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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Familial Alzheimer's Disease
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
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Predisposing Locus for Alzheimer's Disease on Chromosome 21
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Parkinsons Disease and Genetics
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The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
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Complete Genomic Screen in Parkinson Disease
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Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
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Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
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Familial Aggregation in Frontotemporal Dementia
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Hereditary Form of Parkinsonism-Dementia
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Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
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Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
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Preclinical Detection of Parkinson's Disease
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A Large Kindred with Autosomal Dominant Parkinson's Disease
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Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
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Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978
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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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022
Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Spinal Muscular Atrophy
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Alzheimers Disease
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Duchenne Muscular Dystrophy
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Muscular Dystrophies
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017
Molybdenum Cofactor Deficiency
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Red Papules on the Tongue of a Patient with Hemiparesis
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A 52-year-old Woman with Progressive Proximal Weakness
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Sturge-Weber Syndrome
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Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures
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Degenerative Diseases of the Nervous System, Alzheimer Disease
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The Limbic-Girdle Muscular Dystrophies
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Sturge-Weber Syndrome
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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