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Neonatal Seizures
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Huntington Disease: Clinical Features and Diagnosis
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
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Genetic Aspects of Alzheimer Disease
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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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CT in Ceroid Lipofuscinosis
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Thyrotoxic Periodic Paralysis
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