Zobrazeno 1 - 10
of 204
pro vyhledávání: '"sleep-related hypermotor epilepsy"'
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Sleep-related hypermotor epilepsy (SHE) is a focal epilepsy syndrome characterized by a variable age of onset and heterogeneous etiology. Current literature suggests a prevalence rate of approximately 1.8 per 100,000 persons. The discovery of additio
Externí odkaz:
https://doaj.org/article/1c220c90563b49c28f8a79624bdaf700
Publikováno v:
Epilepsy & Behavior Reports, Vol 25, Iss , Pp 100650- (2024)
We consider the disorders of arousal and sleep-related hypermotor epilepsy as genetic twin-conditions, one without, one with epilepsy. They share an augmented arousal-activity during NREM sleep with sleep-wake dissociations, culminating in sleep terr
Externí odkaz:
https://doaj.org/article/8b3ad471d9d44b2097e4e796c621f7f6
Publikováno v:
Archives of Epilepsy, Vol 29, Iss 2, Pp 62-67 (2023)
Sleep-related hypermotor epilepsy (SHE) should be differentiated from NREM parasomnias in terms of a similar clinical presentation. The lack of ictal and/or interictal epileptic encephalographic (EEG) features in SHE complicates the differential diag
Externí odkaz:
https://doaj.org/article/df82bc10ba1a45a9a2b3465464f61f7a
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Differentiating between non-rapid eye movement (NREM) parasomnias and sleep-related hypermotor epilepsy (SHE) is challenging, as they exhibit similar episodes during sleep. A relatively high prevalence of NREM parasomnias has been detected in familie
Externí odkaz:
https://doaj.org/article/66e06dcd65244bbe805f3a504c903549
Publikováno v:
Translational Neuroscience, Vol 13, Iss 1, Pp 240-245 (2022)
Autosomal dominant sleep-related hypermotor epilepsy (ADSHE) is characterized by severe sleep-related rigid hypermotor seizures. The pathogenic genes of ADSHE include genes encoding subunits of the neuronal nicotinic acetylcholine receptor, KCNT1, DE
Externí odkaz:
https://doaj.org/article/3a0dbbbebd714f4882ef7f19385faed7
Publikováno v:
Archives of Epilepsy, Vol 28, Iss 4, Pp 169-171 (2022)
Sleep-related hypermotor epilepsy is a subgroup of sleep-related epilepsies and is very rare among focal epilepsies. It is a type of epilepsy that can be confused with the primary diseases of sleep and is diagnosed late. Here, we present a case diagn
Externí odkaz:
https://doaj.org/article/93be9b4c9d2f4944b06f5cc827e4f115
Publikováno v:
Pharmacological Research, Vol 189, Iss , Pp 106698- (2023)
Despite recent advances in understanding the causes of epilepsy, especially the genetic, comprehending the biological mechanisms that lead to the epileptic phenotype remains difficult. A paradigmatic case is constituted by the epilepsies caused by al
Externí odkaz:
https://doaj.org/article/324ff2a230da4b78ab7abe2e65f0d09a
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Sleep Science and Practice, Vol 3, Iss 1, Pp 1-11 (2019)
Abstract Sleep-related hypermotor epilepsy (SHE), formerly known as Nocturnal Frontal Lobe Epilepsy is a focal epilepsy characterized by seizures with complex hyperkinetic automatisms and/or asymmetric tonic/dystonic posturing occurring mostly during
Externí odkaz:
https://doaj.org/article/df21bb0391004ed9a1f05227d971aeef
Autor:
Carlotta Mutti, Giorgia Bernabè, Noemi Barozzi, Rosario Ciliento, Irene Trippi, Giuseppe Pedrazzi, Nicoletta Azzi, Liborio Parrino
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Introduction: Differential diagnosis between disorders of arousal (DoA) and sleep-related hypermotor epilepsy (SHE) often represents a clinical challenge. The two conditions may be indistinguishable from a semiological point of view and the scalp vid
Externí odkaz:
https://doaj.org/article/40c7232c196f45aba7d146761ab8c449