Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jamal Al Ali"'
Autor:
Jamal Al Ali, Maureen Lacy, Mahesh Padmanaban, Widad Abou Chaar, Hannah Hagy, Peter C. Warnke, Tao Xie
Publikováno v:
Frontiers in Human Neuroscience, Vol 18 (2024)
IntroductionEssential tremor (ET) is a common neurological disease. Deep brain stimulation (DBS) to the thalamic ventral intermediate nucleus (VIM) or the adjacent structures, such as caudal zona incerta/ posterior subthalamic area (cZi/PSA), can be
Externí odkaz:
https://doaj.org/article/67eaa6a852864550861cdd3e1e3bec80
Autor:
Jamal Al Ali, Jessica Yang, Matthew S. Phillips, Joseph Fink, James Mastrianni, Kaitlin Seibert
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Fahr’s disease, or primary familial brain calcification (PFBC), is a rare genetic neurologic disease characterized by abnormal calcification of the basal ganglia, subcortical white matter and cerebellum. Common clinical features include parkinsonis
Externí odkaz:
https://doaj.org/article/76cc926dd14a436baa37f97f7a47fecd
Autor:
Joelle Makoukji, Fadi Saadeh, Karl Albert Mansour, Sally El‐Sitt, Jamal Al Ali, Nihar Kinarivala, Paul C. Trippier, Rose‐Mary Boustany
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 5, Iss 9, Pp 1089-1103 (2018)
Abstract Objective Neuronal Ceroid Lipofuscinoses (NCL) are fatal inherited neurodegenerative diseases with established neuronal cell death and increased ceramide levels in brain, hence, a need for disease‐modifying drug candidates, with potential
Externí odkaz:
https://doaj.org/article/e661f20a7f5146d8aa6824cfbddc37a8
Autor:
Sally El-Sitt, Jihane Soueid, Jamal Al Ali, Joelle Makoukji, Nadine J. Makhoul, Hayat Harati, Rose-Mary Boustany
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
CLN3 disease is a neurodevelopmental disease leading to early visual failure, motor decline, and death. CLN3 pathogenesis has been linked to dysregulation of ceramide, a key intracellular messenger impacting various biological functions. Ceramide is
Externí odkaz:
https://doaj.org/article/be0752e88674435ea5eeae9829ab80f5
Autor:
Jamal Al Ali, Jessica Yang, Matthew S. Phillips, Joseph Fink, James Mastrianni, Kaitlin Seibert
Publikováno v:
Sunday, April 23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcbb30cbebd24f6d78e12dda160c2c4d
https://doi.org/10.1212/wnl.0000000000202000
https://doi.org/10.1212/wnl.0000000000202000
Autor:
Hayat Harati, Bilal Asser, Daniel Daou, Nadine J. Makhoul, Katia Maalouf, Sally El-Sitt, Joelle Makoukji, Jamal Al Ali, Jihane Soueid, Rose-Mary Boustany
Publikováno v:
Annals of Neurology. 86:729-742
Objective CLN3 disease is the commonest of the neuronal ceroid lipofuscinoses, a group of pediatric neurodegenerative disorders. Functions of the CLN3 protein include antiapoptotic properties and facilitating anterograde transport of galactosylcerami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd26c7ec2971d03e8e50864772fb428
https://doi.org/10.1002/ana.25573
https://doi.org/10.1002/ana.25573
Autor:
Jihane Soueid, Jamal Al Ali, Nadine J. Makhoul, Sally El-Sitt, Joelle Makoukji, Rose-Mary Boustany, Hayat Harati
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Frontiers in Neurology
Frontiers in Neurology
CLN3 disease is a neurodevelopmental disease leading to early visual failure, motor decline, and death. CLN3 pathogenesis has been linked to dysregulation of ceramide, a key intracellular messenger impacting various biological functions. Ceramide is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9082ec9cf7529798ec43d7ce1bf11d29
https://doi.org/10.3389/fneur.2019.00128
https://doi.org/10.3389/fneur.2019.00128