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Sleep Transitions in Hypocretin-Deficient Narcolepsy
Author(s) -
Gertrud Laura Sørensen,
Stine Knudsen,
Poul Jennum
Publication year - 2013
Publication title -
sleep
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.222
H-Index - 207
eISSN - 1550-9109
pISSN - 0161-8105
DOI - 10.5665/sleep.2880
Subject(s) - narcolepsy , cataplexy , orexin , non rapid eye movement sleep , psychology , sleep (system call) , polysomnography , sleep disorder , sleep stages , medicine , endocrinology , neurology , neuroscience , eye movement , insomnia , psychiatry , electroencephalography , neuropeptide , receptor , computer science , operating system
Narcolepsy is characterized by instability of sleep-wake, tonus, and rapid eye movement (REM) sleep regulation. It is associated with severe hypothalamic hypocretin deficiency, especially in patients with cataplexy (loss of tonus). As the hypocretin neurons coordinate and stabilize the brain's sleep-wake pattern, tonus, and REM flip-flop neuronal centers in animal models, we set out to determine whether hypocretin deficiency and/or cataplexy predicts the unstable sleep-wake and REM sleep pattern of the human phenotype.

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