Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Tarek El Halabi"'
Autor:
Tarek El Halabi, Maya Dirani, Wassim Nasreddine, Ghassan Hmaimess, Sandra El Sabbagh, Jaafar Wazne, Hassan Toufaili, Dana Hasbini, Ahmad Beydoun
Publikováno v:
Epilepsia Open, Vol 6, Iss 4, Pp 727-735 (2021)
Abstract Objective The aims of this study were to evaluate the frequency of paroxysmal spells of indeterminate nature (PSIN) in a large cohort of children and adults with suspected new‐onset seizures, to evaluate the reasons for including patients
Externí odkaz:
https://doaj.org/article/c101318a88324d1193e7f0d8850a05c0
Publikováno v:
Epilepsia Open, Vol 6, Iss 1, Pp 73-78 (2021)
Abstract Seizure threshold‐2 (SZT2) gene variants have been associated with a decrease in seizure threshold resulting in variable phenotypic expressions ranging from mild‐moderate intellectual disabilities without seizures, to an early‐onset ep
Externí odkaz:
https://doaj.org/article/1c9787ed998e4daa8e5929beb7c197c4
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Action myoclonus-renal failure syndrome (AMRF) is a rare, recessively inherited form of progressive myoclonus epilepsy (PME) caused by mutations in the SCARB2 gene and associated with end-stage renal failure. In addition to severe progressive myoclon
Externí odkaz:
https://doaj.org/article/9c6d0eb999d145e4a6bf84b7735a26f4
Autor:
Sahar Farhat, Tarek El Halabi, Achraf Makki, Samir F. Atweh, Wassim Nasreddine, Ahmad Beydoun
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Baclofen, a muscle relaxant prescribed for the alleviation of symptoms of spasticity acts primarily at the spinal level but with high doses, it penetrates the blood-brain barrier and can result in prominent central nervous depression. Baclofen toxici
Externí odkaz:
https://doaj.org/article/477c3d96df70403787cc47b13a0b4f63
Publikováno v:
Case Reports in Neurological Medicine, Vol 2020 (2020)
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is an inherited disorder caused by a mutation in the NOTCH 3 gene, characterized by early onset of subcortical lacunar infarcts in the absence of vas
Externí odkaz:
https://doaj.org/article/0be5d81316da47eaaee09b4d4f50dba1
Autor:
Najo Jomaa, Tarek El Halabi, Jawad Melhem, Georgette Dib, Youssef Ghosn, Mukbil Hourani, Wassim Nasreddine, Ahmad Beydoun
Publikováno v:
The Neurohospitalist. 12:371-376
Background: Coronavirus disease 2019 (COVID-19) has been associated with many neurological complications affecting the central nervous system. Purpose: Our aim was to describe a case of COVID-19 associated with a probable variant of acute necrotizing
Autor:
Nada R Chedid, Joseph E. Makzoumé, Wassim El-Khatib, Jean-Michel Saadé, Fadi El-Hage, Mohammad Tarek El-Halabi
Publikováno v:
Journal of Dental Education. 86:393-400
PURPOSE Self-assessment is increasingly implemented in medical professions' curricula. In this research, the authors measure the effects of self-assessment within a preclinical removable prosthodontics course among dental students in a private dental
Publikováno v:
Epilepsia Open, Vol 6, Iss 1, Pp 73-78 (2021)
Epilepsia Open
Epilepsia Open
Seizure threshold‐2 (SZT2) gene variants have been associated with a decrease in seizure threshold resulting in variable phenotypic expressions ranging from mild‐moderate intellectual disabilities without seizures, to an early‐onset epileptic e
Publikováno v:
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society. 39(5)
Hypoxic-ischemic brain injury is a well-known consequence of cardiac arrest and providing an accurate prognostication remains a challenge, especially in decisions related to withdrawal of care. Bilateral absence of the cortical response (N20 potentia
Publikováno v:
Pain Medicine. 22:1707-1709