Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Elie, Abdelnour"'
Autor:
Ashley R. Helseth, Arsen S. Hunanyan, Syed Adil, Molly Linabarger, Monisha Sachdev, Elie Abdelnour, Eric Arehart, Marlee Szabo, Jordan Richardson, William C. Wetsel, Ute Hochgeschwender, Mohamad A. Mikati
Publikováno v:
Neurobiology of Disease, Vol 119, Iss , Pp 100-112 (2018)
De novo mutations causing dysfunction of the ATP1A3 gene, which encodes the α3 subunit of Na+/K+-ATPase pump expressed in neurons, result in alternating hemiplegia of childhood (AHC). AHC manifests as paroxysmal episodes of hemiplegia, dystonia, beh
Externí odkaz:
https://doaj.org/article/66f13110be214ed7ba820e4483357442
Publikováno v:
Mo Med
The prevalence of Attention Deficit Hyperactivity Disorder (ADHD) has seen a consistent rise in recent years. These numbers spark a debate over the reason for the observed trends, with some concerned about over diagnosis and over prescription of stim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ac38060ceea7d1008e29ac9d8e8a218
https://pubmed.ncbi.nlm.nih.gov/36337990
https://pubmed.ncbi.nlm.nih.gov/36337990
Autor:
Milton Pratt, Melanie J. Bonner, Julie Uchitel, Geraldine Dawson, April Boggs, Lyndsey Prange, Joan Jasien, Mohamad A. Mikati, Tavis Abrahamsen, Elie Abdelnour
Publikováno v:
Developmental Medicine & Child Neurology. 62:820-826
AIM To evaluate presence and severity of social impairments in alternating hemiplegia of childhood (AHC) and determine factors that are associated with social impairments. METHOD This was a retrospective analysis of 34 consecutive patients with AHC (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fceb8152520bdd51bfde4a9c5b58af26
https://doi.org/10.1111/dmcn.14473
https://doi.org/10.1111/dmcn.14473
Autor:
Eric Arehart, Monisha Sachdev, Molly Linabarger, Syed M Adil, Ute Hochgeschwender, Jordan Richardson, Ashley Helseth, Elie Abdelnour, William C. Wetsel, Arsen S. Hunanyan, Marlee Szabo, Mohamad A. Mikati
Publikováno v:
Neurobiology of Disease, Vol 119, Iss, Pp 100-112 (2018)
De novo mutations causing dysfunction of the ATP1A3 gene, which encodes the α3 subunit of Na+/K+-ATPase pump expressed in neurons, result in alternating hemiplegia of childhood (AHC). AHC manifests as paroxysmal episodes of hemiplegia, dystonia, beh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d262c1fdc5ce01b722bb1817a4e01aae
http://www.sciencedirect.com/science/article/pii/S0969996118303504
http://www.sciencedirect.com/science/article/pii/S0969996118303504
Autor:
Scott D. Moore, Monisha Sachdev, Qiang Li, Melanie Masoud, Mohamad A. Mikati, Elie Abdelnour, Jordan Richardson, Arsen S. Hunanyan, Leeyup Chung, J. Victor Nadler, Ashley Helseth, Bassil Kherallah
Publikováno v:
Epilepsia. 59:1455-1468
Objective Na+ /K+ -ATPase dysfunction, primary (mutation) or secondary (energy crisis, neurodegenerative disease) increases neuronal excitability in the brain. To evaluate the mechanisms underlying such increased excitability we studied mice carrying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcd6a65b8d80b115a35f024a6b6f1c0e
https://doi.org/10.1111/epi.14441
https://doi.org/10.1111/epi.14441
Autor:
Roger E. McLendon, Mohamad A. Mikati, Eric Arehart, Rodney A. Radtke, Edward C. Smith, Elie Abdelnour, Sujay Kansagra, Carolyn Pizoli, William Gallentine, Anthony Pecoraro
Publikováno v:
Epilepsy & Behavior. 73:137-141
Objectives To describe the characteristics of epilepsy in patients with Neurofibromatosis type 1 (NF1). Methods Analysis of a cohort of consecutive NF1 patients seen in our NF1 clinic during a three-year period. Results Of the 184 NF1 patients seen d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe801839a6e7c726a583a20956004c7c
https://doi.org/10.1016/j.yebeh.2017.05.011
https://doi.org/10.1016/j.yebeh.2017.05.011
Autor:
Melissa McLean, Ryan Ghusayni, Tavis Abrahamsen, Mohamad A. Mikati, Allen W. Song, Jeffrey R. Petrella, Lyndsey Prange, Elie Abdelnour, Jordan Richardson, Julie Uchitel
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 26
Quantitative MRI is increasingly being used as a biomarker in neurological disorders. Cerebellar atrophy occurs in some Alternating Hemiplegia of Childhood (AHC) patients. However, it is not known if cerebellar atrophy can be a potential biomarker in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b089267dab3c7aae1d2146931f407e3e
https://pubmed.ncbi.nlm.nih.gov/32376083
https://pubmed.ncbi.nlm.nih.gov/32376083
Autor:
Arsen S, Hunanyan, Ashley R, Helseth, Elie, Abdelnour, Bassil, Kherallah, Monisha, Sachdev, Leeyup, Chung, Melanie, Masoud, Jordan, Richardson, Qiang, Li, J Victor, Nadler, Scott D, Moore, Mohamad A, Mikati
Publikováno v:
Epilepsia. 59(7)
NaWe performed extracellular recordings, as well as whole-cell patch clamp recordings from pyramidal cells and interneurons, in the CA1 region on hippocampal slices. We also performed immunohistochemistry from hippocampal sections to count CA1 pyrami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ee210ebf316e1093dd93f74d0507217
https://pubmed.ncbi.nlm.nih.gov/29889309
https://pubmed.ncbi.nlm.nih.gov/29889309
Autor:
Rosanna Forteza, Demet Toprak, Ye Cui, Hilary J. Goldberg, Souheil El-Chemaly, Ivan O. Rosas, Hao Wang, Elie Abdelnour, Emmanuel D’Agostino, Gary A. Visner, Mark A. Perrella, Robert F. Padera, Gautam George, Kaifeng Liu, Maria E. Monzon-Medina
Publikováno v:
Journal of Clinical Investigation. 125:4255-4268
Lung transplantation is the only viable option for patients suffering from otherwise incurable end-stage pulmonary diseases such as chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. Despite aggressive immunosuppression, acute r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f0aec4fc57cbf222856c8759211cb2
https://doi.org/10.1172/jci79693
https://doi.org/10.1172/jci79693