Results 11 to 20 of about 7,855 (207)

Age at Onset and Delays in Diagnosis of Central Disorders of Hypersomnolence Over the Past 30 Years. [PDF]

J Sleep Res
ABSTRACT Patients with narcolepsy type 1 (NT1), type 2 (NT2), idiopathic hypersomnia (IH) usually suffer from symptoms for years, even decades, before being diagnosed. We aimed to assess age at onset, age at diagnosis and changes in the diagnostic delays of these patients from 1990 to 2020 in a single centre.
Zhang Z, Barateau L, Béziat S, Khatami R, Dauvilliers Y.   +4 more
europepmc   +2 more sources

The Genetics of Sleep Disorders in Children: A Narrative Review

Brain Sciences, 2021
Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them.
Greta Mainieri, Angelica Montini, Antonio Nicotera, Gabriella Di Rosa, Federica Provini, Giuseppe Loddo   +5 more
doaj   +1 more source

Pharmacological Treatments of Sleep–Wake Disorders: Update 2023

Clinical and Translational Neuroscience, 2023
Biological, environmental, behavioral, and social factors can influence sleep and lead to sleep disorders or diseases. Sleep disorders are common, numerous, and heterogeneous in terms of their etiology, pathogenesis, and symptomatology. The management of
Marcel S. Kallweit, Nayeli P. Kallweit, Ulf Kallweit   +2 more
doaj   +1 more source

Palliative Care in Europe: Safeguarding Compassion Amidst Changing End-of-Life Policies and Expanding Access to Medically Assisted Dying Position Statement on behalf of the European Academy of Neurology, the European Federation of Neurological Associations and OneNeurology. [PDF]

Eur J Neurol
European Journal of Neurology, Volume 33, Issue 4, April 2026.
Rukavina K, de Visser M, Moro E, Bhatia K, Boon P, Midelfart-Hoff J, Leonardi M, Rektorova I, Fink GR, Nasr N, Gonzalez-Martinez A, Bassetti CLA, Kallweit U, Crean M, Cras P, Vanopdenbosch L, Arnesen A, Jaarsma J, Kowski AB, Veronese S, Oliver D, European Academy of Neurology, the European Federation of Neurological Associations, OneNeurology.   +23 more
europepmc   +2 more sources

Are there sleep-specific phenotypes in patients with chronic fatigue syndrome? A cross-sectional polysomnography analysis [PDF]

, 2013
Objectives: Despite sleep disturbances being a central complaint in patients with chronic fatigue syndrome (CFS), evidence of objective sleep abnormalities from over 30 studies is inconsistent.
Deary, Vincent, Ellis, Jason, Gotts, Zoe, Newton, Julia   +3 more
core   +1 more source

Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1

Frontiers in Neurology, 2021
Myotonic dystrophy type 1 is the most common form of muscular dystrophy in adults, and is primarily characterized by muscle weakness and myotonia, yet some of the most disabling symptoms of the disease are cognitive and behavioral.
Jacob N. Miller, Alison Kruger, David J. Moser, Laurie Gutmann, Ellen van der Plas, Timothy R. Koscik, Sarah A. Cumming, Darren G. Monckton, Peggy C. Nopoulos, Peggy C. Nopoulos, Peggy C. Nopoulos   +10 more
doaj   +1 more source

Protocol of the SOMNIA project : an observational study to create a neurophysiological database for advanced clinical sleep monitoring [PDF]

, 2019
Introduction Polysomnography (PSG) is the primary tool for sleep monitoring and the diagnosis of sleep disorders. Recent advances in signal analysis make it possible to reveal more information from this rich data source.
Arsenali, Bruno, Bergmans, Jan W. M., Fonseca, Pedro, Haakma, Reinder, Hoondert, Bertram, Krijn, Roy, Lauwerijssen, Coen, Leufkens, Tim R., Maass, Henning, Overeem, Sebastiaan, Pevernagie, Dirk, Pillen, Sigrid, van den Heuvel, Leonie, van Dijk, Johannes P., van Gilst, Merel M., van Sloun, Ruud J. G., Vandenbussche, Nele   +16 more
core   +2 more sources

Identification of Additional Cases of Severe Neonatal GABA-Transaminase Deficiency. [PDF]

JIMD Rep
ABSTRACT GABA‐transaminase (GABA‐T) deficiency is a rare disorder of GABA metabolism characterized by neonatal encephalopathy, epilepsy, hypotonia and intellectual disability. It is caused by biallelic pathogenic variants in the ABAT gene. We report a case of a newborn female born to a G10P5 mother, with abnormal fetal movements and polyhydramnios in ...
Alammary D, Low T, Srinivasan G, Dery MC, Almutadares M, Marin S, Rafay MF, Rozovsky K, Frosk P.   +8 more
europepmc   +2 more sources

Narcolepsy with cataplexy after A/H1N1 vaccination – A case reported from Cuba

Sleep Science, 2014
Narcolepsy with cataplexy is a rare sleep disorder with a neurological basis which has been recently linked to H1N1 vaccination either in children or adults. Cases from Europe, United States and Brasil were registered. Authors describe a case report of a
Yaimi Rosales Mesa, Miguel Gonçalves Meira e Cruz   +1 more
doaj   +1 more source

Hypersomnolence in Wilson Disease [PDF]

Journal of Clinical Sleep Medicine, 2015
Wilson disease (WD) is an autosomal recessive disorder of copper metabolism resulting in copper accumulation in a number of organs including the liver, brain, and cornea, predominantly leading to hepatic, neurologic, and psychiatric manifestations. An association between WD and sleep problems is not commonly recognized, and sleep complaints are often ...
Valerie C, Amann, Neal K, Maru, Vivek, Jain   +2 more
openaire   +2 more sources