Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mohamed Jailani"'
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
DeSanto-Shinawi syndrome is a rare genetic condition caused by loss-of-function mutation in WAC. It is characterized by dysmorphic features, intellectual disability, and behavioral abnormalities. In this case report, we describe the clinical features
Externí odkaz:
https://doaj.org/article/d802b00000344f298585e9b5a91e9a48
Autor:
Mohamed Jailani, Mohamed Mubarak, Mariam Sarkhouh, Ahmed Al Mahrezi, Habib Abdulnabi, Mohamed Naiser, Husain Alaradi, Abdulaziz Alabbad, Maram Hassan, Amer Kamal
Publikováno v:
Behavioral Sciences, Vol 10, Iss 2, p 43 (2020)
Introduction: Caffeine, an adenosine-receptor blocker, is believed to have neuronal excitatory effects, while Taurine, a mammalian amino acid, was shown to have neuroinhibitory effects. Aim: The aim of this study was to investigate the effects of acu
Externí odkaz:
https://doaj.org/article/a5c071d53f01426b8cd737e1fa76fce4
Autor:
Mahmoud Barbarawi, Owais Barbarawi, Mohamed Jailani, Ahmad Al-abdouh, Mahammed Mhanna, Peter Robinson
Publikováno v:
Coronary Artery Disease. 34:274-280
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8246ae5bbc1ce2dc60df4410b42d973
https://doi.org/10.1097/mca.0000000000001236
https://doi.org/10.1097/mca.0000000000001236
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d1843b1dd329e2c739214e5534b1480
https://doi.org/10.7759/cureus.32836
https://doi.org/10.7759/cureus.32836
Autor:
Mahmoud Barbarawi, Owais Barbarawi, Mohamed Jailani, Ahmad Al-abdouh, Mahammed Mhanna, Peter Robinson
Publikováno v:
JACC: Cardiovascular Interventions. 16:S44-S45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7ff62a27561eac00e9c1d5fe29219ca
https://doi.org/10.1016/j.jcin.2023.01.148
https://doi.org/10.1016/j.jcin.2023.01.148
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2020 (2020)
Case Reports in Pediatrics, Vol 2020 (2020)
DeSanto-Shinawi syndrome is a rare genetic condition caused by loss-of-function mutation in WAC. It is characterized by dysmorphic features, intellectual disability, and behavioral abnormalities. In this case report, we describe the clinical features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c15c3e47726ec8836d1b03114ef18dce
https://doi.org/10.1155/2020/8820966
https://doi.org/10.1155/2020/8820966
Autor:
Abdulaziz Alabbad, Mariam Sarkhouh, Maram Hassan, Ahmed Al Mahrezi, Mohamed Jailani, Mohamed Naiser, Husain Alaradi, Mohamed Mubarak, Habib Abdulnabi, Amer Kamal
Publikováno v:
Behavioral Sciences, Vol 10, Iss 2, p 43 (2020)
Behavioral Sciences
Volume 10
Issue 2
Behavioral Sciences
Volume 10
Issue 2
Introduction: Caffeine, an adenosine-receptor blocker, is believed to have neuronal excitatory effects, while Taurine, a mammalian amino acid, was shown to have neuroinhibitory effects. Aim: The aim of this study was to investigate the effects of acu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a989ea4ed8276900cc0fe43c8b0a84a
https://www.mdpi.com/2076-328X/10/2/43
https://www.mdpi.com/2076-328X/10/2/43
Autor:
Mohamed Jailani, Laila Ben Lamine, Wassim Y. Almawi, Sameh Sarray, Amira Turki, Touhami Mahjoub, Mohamed Ghorbel, Hagger B. Amor, Ghada Al-Khateeb, Nejla Sellami
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 128:319-324
Background To investigate the relationship between changes in circulating soluble CD40 ligand (sCD40L) levels and the presence and severity of type 2 diabetic retinopathy (DR). Subjects and methods sCD40L plasma concentrations were measured in 205 ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad2f088aa8b685324206c18eefbae65
https://doi.org/10.1055/a-0647-6860
https://doi.org/10.1055/a-0647-6860
Autor:
Halla F. Bakheit, Maram Atallah Alharbi, Bashayer H. Ebrahin, Mohamed Jailani, Ghada Al-Kafaji, Ahmad A. Farahat, Moiz Bakhiet
Publikováno v:
Neuromolecular medicine. 22(2)
The impaired mitochondrial function has been implicated in the pathogenicity of multiple sclerosis (MS), a chronic inflammatory, demyelinating, and neurodegenerative disease of the CNS. Circulating mtDNA copy number in body fluids has been proposed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7341a37fa41f3430211b2e9e3e51dcd0
https://pubmed.ncbi.nlm.nih.gov/31902116
https://pubmed.ncbi.nlm.nih.gov/31902116
Publikováno v:
Indian Journal of Public Health Research & Development. 10:633
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea011332f3c7d281434f087526e368d0
https://doi.org/10.5958/0976-5506.2019.00124.4
https://doi.org/10.5958/0976-5506.2019.00124.4