Results 71 to 80 of about 1,328,941 (179)

MONOSEMPTOMATİK KLEINE-LEVIN SENDROMU: Bir Olgu Sunumu

open access: yesCerrahpaşa Medical Journal, 2014
Background.- Kleine-Levin syndrome is characterized by recurring episodes of hypersomnia, mental disturbances and abnormal behaviour including hyperphagia and hypersexuality.
Derya KARADENiZ   +5 more
doaj  

Sleep‐related disorders in children: A narrative review

open access: yesPediatric Discovery, Volume 2, Issue 2, June 2024.
Abstract Sleep‐related disorders in children can significantly impact children's physical, emotional, and cognitive development and constitute a major source of parental concern. This comprehensive review aims to describe sleep‐related disorders commonly encountered in pediatric practice, their etiology, diagnosis, and management strategies. The review
Yogev Cohen   +2 more
wiley   +1 more source

New hypothesis on pontine-frontal eye field connectivity in Kleine-Levin syndrome

open access: yes, 2016
Previous studies have indicated involvement of the thalamus and the pons in Kleine-Levin syndrome. In the present study, functional connectivity of the thalamus and the pons was investigated in asymptomatic patients with Kleine-Levin syndrome and healthy
Karlsson, Thomas   +5 more
core   +1 more source

Kleine-Levin syndrome: interface between neurology and psychiatry Síndrome de Kleine-Levin: interface entre neurologia e psiquiatria

open access: yesArquivos de Neuro-Psiquiatria, 2007
We report the first episode of Kleine-Levin (KLS) syndrome in a 17-year-old male. The illness onset, clinical features, neuropsychological evaluation and polysomnographic recording are described.
Luís Pereira Justo   +3 more
doaj   +1 more source

Functional recovery after ischemic stroke: Impact of different sleep health parameters

open access: yesJournal of Sleep Research, Volume 33, Issue 1, February 2024.
Summary Sleep disturbances after ischaemic stroke include alterations of sleep architecture, obstructive sleep apnea, restless legs syndrome, daytime sleepiness and insomnia. Our aim was to explore their impacts on functional outcomes at month 3 after stroke, and to assess the benefit of continuous positive airway pressure in patients with severe ...
Claire Denis   +13 more
wiley   +1 more source

Idiopathic hypersomnia, Kleine–Levin syndrome, and symptomatic hypersomnias

open access: yes, 2017
Besides obstructive sleep apnea syndrome and narcolepsy, there are a number of other causes of excessive daytime sleepiness, listed in the International Classification of Sleep Disorders, third edition, as central disorders of hypersomnolence.
Michel Billiard, Yves Dauvilliers
core   +1 more source

Kleine-Levin syndrome as a neuropsychiatric presentation: A case report and review

open access: yesSouth African Journal of Psychiatry, 2014
Kleine-Levin syndrome (KLS) is a rare disorder characterised by hypersomnia, hyperphagia and behavioural disturbances. It typically occurs in adolescent men and may mimic a variety of neuropsychiatric conditions.
Anusha Lachman
doaj   +1 more source

Short-term memory dysfunction in Kleine-Levin syndrome

open access: yes, 2003
Background - A previous investigation at our department of a young man with typical Kleine-Levin syndrome revealed short-term memory dysfunction as well as hypoperfusion of the temporal lobes on single photon emission tomography (SPECT) (CERETECR ...
Schwerdt, K   +4 more
core   +1 more source

Kleine-levin syndrome: A rare case and review

open access: yesAnnals of Indian Psychiatry, 2019
Kleine–Levin syndrome (KLS), also known as sleeping beauty syndrome, is a rare disorder with unknown etiology. The syndrome is characterized by hypersomnolence and may be associated with hypersexuality, hyperphagia and cognitive or mood changes.
Falguni B Patel   +3 more
doaj   +1 more source

Periodic hypersomnia, congenital ectodermal disorders and multiple exostosis

open access: yesArquivos de Neuro-Psiquiatria, 1989
A case of periodic hypersomnia in an 11-year-old female with the unique features of mental deficiency, incontinentia pigmenti, acanthosis nigricans and hereditary multiple exostosis (diaphysial aclasis) is reported.
Rubens Reimão, Aron Diament
doaj   +1 more source

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