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

Mohammed M Jan

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Saudi Journal of Biological Sciences|October 26, 2020
Next generation sequencing reveals novel homozygous frameshift in <i>PUS7</i> and splice acceptor variants in <i>AASS</i> gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephalyMuhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Mohammed M Jan, et al.
Neurosciences (Riyadh, Saudi Arabia)|June 17, 2011
Pediatric electroencephalography. Parent`s knowledge and experienceZaitoon M Shivji, Marwa M Al-Baharna, Ghada A Kadi, et al.
Journal of the Neurological Sciences|November 23, 2016
A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi familyMuhammad Imran Naseer, Mahmood Rasool, Mohammed M Jan, et al.
Neurosciences (Riyadh, Saudi Arabia)|October 22, 2013
Parents` knowledge and attitudes toward children with epilepsyLama E Zainy, Daniah M Atteyah, Walaa M Aldisi, et al.
Neurosciences (Riyadh, Saudi Arabia)|July 16, 2018
Treatment of infantile spasms in Saudi ArabiaMaryam A Alqassas, Osama Y Muthaffar, Anan A Aljawi, et al.
Seizure|January 22, 2014
Primary school teacher's knowledge and attitudes toward children with epilepsyAlbaraa S Abulhamail, Fahad E Al-Sulami, Mouneeb A Alnouri, et al.
Pediatric Neurology|February 11, 2014
Intravenous methylprednisolone for intractable childhood epilepsyKholoud H Almaabdi, Rawan O Alshehri, Areej A Althubiti, et al.
BMC Genomics|April 30, 2015
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi ArabiaMuhammad Imran Naseer, Muhammad Faheem, Adeel G Chaudhary, et al.
BMC Genomics|October 22, 2016
Copy number variations in Saudi family with intellectual disability and epilepsyMuhammad I Naseer, Adeel G Chaudhary, Mahmood Rasool, et al.
Pediatric Health, Medicine and Therapeutics|December 21, 2018
Parental perceptions of dental health and need for treatment in children with epilepsy: a multicenter cross-sectional studyAhmed Hussein Subki, Abdel Moniem Mukhtar, Omar M Saggaf, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Saudi Journal of Biological Sciences|October 26, 2020
Next generation sequencing reveals novel homozygous frameshift in <i>PUS7</i> and splice acceptor variants in <i>AASS</i> gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephalyMuhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Mohammed M Jan, et al.
Neurosciences (Riyadh, Saudi Arabia)|June 17, 2011
Pediatric electroencephalography. Parent`s knowledge and experienceZaitoon M Shivji, Marwa M Al-Baharna, Ghada A Kadi, et al.
Journal of the Neurological Sciences|November 23, 2016
A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi familyMuhammad Imran Naseer, Mahmood Rasool, Mohammed M Jan, et al.
Neurosciences (Riyadh, Saudi Arabia)|October 22, 2013
Parents` knowledge and attitudes toward children with epilepsyLama E Zainy, Daniah M Atteyah, Walaa M Aldisi, et al.
Neurosciences (Riyadh, Saudi Arabia)|July 16, 2018
Treatment of infantile spasms in Saudi ArabiaMaryam A Alqassas, Osama Y Muthaffar, Anan A Aljawi, et al.
Seizure|January 22, 2014
Primary school teacher's knowledge and attitudes toward children with epilepsyAlbaraa S Abulhamail, Fahad E Al-Sulami, Mouneeb A Alnouri, et al.
Pediatric Neurology|February 11, 2014
Intravenous methylprednisolone for intractable childhood epilepsyKholoud H Almaabdi, Rawan O Alshehri, Areej A Althubiti, et al.
BMC Genomics|April 30, 2015
Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi ArabiaMuhammad Imran Naseer, Muhammad Faheem, Adeel G Chaudhary, et al.
BMC Genomics|October 22, 2016
Copy number variations in Saudi family with intellectual disability and epilepsyMuhammad I Naseer, Adeel G Chaudhary, Mahmood Rasool, et al.
Pediatric Health, Medicine and Therapeutics|December 21, 2018
Parental perceptions of dental health and need for treatment in children with epilepsy: a multicenter cross-sectional studyAhmed Hussein Subki, Abdel Moniem Mukhtar, Omar M Saggaf, et al.
Pageof 7