Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Ruba Benini"'
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 38, Iss 1, Pp 449-459 (2024)
Abstract Background Juvenile idiopathic epilepsy (JIE) is categorized as a generalized epilepsy. Epilepsy classification entails electrocortical characterization and localization of epileptic discharges (ED) using electroencephalography (EEG). Hypoth
Externí odkaz:
https://doaj.org/article/7148cfc089d04c72a39d6ae10f1022c6
Autor:
Tatiana Vinardell, Sami Elestwani, Camilla Jamieson, Ejaz Karim, Matthew Robin, Sarah Glynn, Ruba Benini, Monica Aleman
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 37, Iss 3, Pp 1209-1215 (2023)
Abstract Background A standardized protocol for electroencephalography (EEG) under standing sedation for the investigation of epilepsy in foals is needed. Hypothesis/Objectives To evaluate a modified standardized EEG protocol under standing sedation
Externí odkaz:
https://doaj.org/article/e48857bc9d2c4ca68c391e75a1fcca85
Publikováno v:
Neurobiology of Disease, Vol 87, Iss , Pp 1-10 (2016)
We obtained field, K+ selective and “sharp” intracellular recordings from the rat entorhinal (EC) and perirhinal (PC) cortices in an in vitro brain slice preparation to identify the events occurring at interictal-to-ictal transition during 4-amin
Externí odkaz:
https://doaj.org/article/eb453226e9a94b6ba7ada5056c9b062e
Publikováno v:
Neurobiology of Disease, Vol 67, Iss , Pp 97-106 (2014)
Mesial temporal lobe epilepsy (MTLE) is characterized in humans and in animal models by a seizure-free latent phase that follows an initial brain insult; this period is presumably associated to plastic changes in temporal lobe excitability and connec
Externí odkaz:
https://doaj.org/article/00730c7bbda54feea6400e6929670bff
Autor:
Abeer Fadda, Mohamed Alsabbagh, Dhanya Vasudeva, Amira Saeed, Sara Aglan, Satanay Z Hubrack, Ruba Benini, Bernice Lo, Khaled Zamel
Epilepsy is one of the most common neurological disorders. The cost to the health system and the impact on quality of life for patients with intractable epilepsies and associated comorbidities is significant. Disease etiology and pathogenesis are sti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a47f12a03da7f5228548f4265d72033
https://doi.org/10.21203/rs.3.rs-2358929/v1
https://doi.org/10.21203/rs.3.rs-2358929/v1
Autor:
Ali Al Wadei, Adel A H Mahmoud, Nahed Lubbad, Ruba Benini, Shoaa Al Enazi, Lamya Jad, Ali Dhohyan Al Otaibi, Sadia Tabassum
Publikováno v:
Pediatric neurology. 119
Background Levetiracetam is a relatively new-generation antiseizure drug approved for the treatment of focal and generalized seizures. Despite its favorable side effect profile and minimal drug-drug interactions, neuropsychiatric side effects are rep
Autor:
Abdulaziz Al-Saman, Mohammed Almannai, Matthew A. Lines, Amal Alhashem, Panagiotis Katsonis, Yaser I. Aljadhai, Julia Wang, Brahim Tabarki, Ayman W. El-Hattab, Mohammed A. Saleh, Adel A H Mahmoud, Ruba Benini, Dorothy K. Grange, Ali H Alwadei, Eissa Faqeih, Lee-Jun C. Wong, Hongzheng Dai, Ali Al Asmari, Olivier Lichtarge
Publikováno v:
Molecular Genetics and Metabolism. 125:281-291
An increasing number of mitochondrial diseases are found to be caused by pathogenic variants in nuclear encoded mitochondrial aminoacyl-tRNA synthetases. FARS2 encodes mitochondrial phenylalanyl-tRNA synthetase (mtPheRS) which transfers phenylalanine
Publikováno v:
Neurobiology of Disease, Vol 67, Iss, Pp 97-106 (2014)
Mesial temporal lobe epilepsy (MTLE) is characterized in humans and in animal models by a seizure-free latent phase that follows an initial brain insult; this period is presumably associated to plastic changes in temporal lobe excitability and connec
Publikováno v:
European Journal of Paediatric Neurology. 18:301-307
Aim The fetal neuroinflammatory response has been linked to the development of brain injury in newborns and subsequent neurologic impairment. We aimed to explore the maternal and child factors associated with histologic chorioamnionitis in cerebral p
Autor:
Ali H Alwadei, Majid Alfadhel, Ali Alasmari, Adel A H Mahmoud, Ruba Benini, Erik-Jan Kamsteeg
Publikováno v:
Developmental Medicine & Child Neurology, 58, 1317-1322
Developmental Medicine & Child Neurology, 58, 12, pp. 1317-1322
Developmental Medicine & Child Neurology, 58, 12, pp. 1317-1322
Item does not contain fulltext Inherited aberrancies in intracellular vesicular transport are associated with a variety of neurological and non-neurological diseases. RUSC2 is a gene found on chromosome 9p13.3 that codes for iporin, a ubiquitous prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7121e4fded97144bed4185136518341a
https://doi.org/10.1111/dmcn.13250
https://doi.org/10.1111/dmcn.13250