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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Clinical Manifestations of the anti-IgLON5 Disease
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A Case of Refractory Nocturnal Seizures
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Anti-DPPX Encephalitis,Pathogenic Effects of Antibodies on Gut and Brain Neurons
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A 75-Year-Old Man With Cognitive Impairment and Gait Changes, Lewy Body Disease
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Managing the Late Complications of Parkinson's Disease
Neurol 49:549-557, Waters,C.H., 1997
Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Sleep Paralysis
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
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Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990
Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
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Narcolepsy-Cataplexy
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Obstructive Sleep Apnea in Family Members
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