Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Faisal Al Azri

Showing results (21-30 of 27) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 27 results.
Dementia and Geriatric Cognitive Disorders Extra|September 10, 2014
Cognitive profiles in patients with multi-infarct dementia: an omani studySamir Al-Adawi, Nady Braidy, Musthafa Essa, et al.
Sultan Qaboos University Medical Journal|September 1, 2023
Identification of Asymptomatic Severe Acute Respiratory Syndrome Coronavirus 2 Infections Among Healthcare Workers at Sultan Qaboos University Hospital, OmanAmal Al Shibli, Mahmood Al Jufaili, Awatif Al Alawi, et al.
BMC Neurology|November 25, 2016
A regional consensus recommendation on brain atrophy as an outcome measure in multiple sclerosisRaed Alroughani, Dirk Deleu, Khalid El Salem, et al.
Open Forum Infectious Diseases|March 4, 2015
Varicella zoster virus pneumonitis and brainstem encephalitis without skin rash in an immunocompetent adultRamachandiran Nandhagopal, Nelly Khmeleva, B Jayakrishnan, et al.
Oman Medical Journal|October 28, 2020
"Virtual Interdisciplinary COVID-19 Team": A Hospital Pandemic Preparedness ApproachAbdullah Balkhair, Mahmoud Al Jufaili, Khalifa Al Wahaibi, et al.
Brain : a Journal of Neurology|January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesisMustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
Acta Neuropathologica|December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseasesElena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Dementia and Geriatric Cognitive Disorders Extra|September 10, 2014
Cognitive profiles in patients with multi-infarct dementia: an omani studySamir Al-Adawi, Nady Braidy, Musthafa Essa, et al.
Sultan Qaboos University Medical Journal|September 1, 2023
Identification of Asymptomatic Severe Acute Respiratory Syndrome Coronavirus 2 Infections Among Healthcare Workers at Sultan Qaboos University Hospital, OmanAmal Al Shibli, Mahmood Al Jufaili, Awatif Al Alawi, et al.
BMC Neurology|November 25, 2016
A regional consensus recommendation on brain atrophy as an outcome measure in multiple sclerosisRaed Alroughani, Dirk Deleu, Khalid El Salem, et al.
Open Forum Infectious Diseases|March 4, 2015
Varicella zoster virus pneumonitis and brainstem encephalitis without skin rash in an immunocompetent adultRamachandiran Nandhagopal, Nelly Khmeleva, B Jayakrishnan, et al.
Oman Medical Journal|October 28, 2020
"Virtual Interdisciplinary COVID-19 Team": A Hospital Pandemic Preparedness ApproachAbdullah Balkhair, Mahmoud Al Jufaili, Khalifa Al Wahaibi, et al.
Brain : a Journal of Neurology|January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesisMustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
Acta Neuropathologica|December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseasesElena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
Pageof 3