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Khalid Hundallah

Showing results (11-20 of 25) with videos related to

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European Journal of Pediatrics|March 17, 2023
Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature reviewMusaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, et al.
BMC Neurology|July 7, 2023
Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitisRaid Hommady, Abdullah Alsohibani, Ruba Alayed, et al.
Seizure|May 5, 2019
The landscape of early infantile epileptic encephalopathy in a consanguineous populationMarwan Nashabat, Xena S Al Qahtani, Salwa Almakdob, et al.
Frontiers in Pediatrics|March 8, 2021
Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 PandemicAhmed K Bamaga, Fouad Alghamdi, Nahla Alshaikh, et al.
American Journal of Medical Genetics. Part A|July 26, 2017
Congenital disorders of glycosylation: The Saudi experienceSarah Alsubhi, Amal Alhashem, Eissa Faqeih, et al.
Brain Communications|September 24, 2021
Homozygous missense <i>WIPI2</i> variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease courseReza Maroofian, Andrea Gubas, Rauan Kaiyrzhanov, et al.
Journal of Medical Genetics|August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Seizure|March 3, 2024
Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statementFahad A Bashiri, Khalid Hundallah, Raidah Al-Baradie, et al.
Journal of Child Neurology|December 1, 2025
Clinical and Genetic Spectrum of <i>SCN8A</i>-Related Disorders: A Retrospective Study From the Gulf RegionOsama Muthaffar, Mashael Alsubhan, Ali Mir, et al.
Pediatric Neurology|July 16, 2022
Hereditary Hyperekplexia in Saudi ArabiaAmal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
European Journal of Pediatrics|March 17, 2023
Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature reviewMusaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, et al.
BMC Neurology|July 7, 2023
Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitisRaid Hommady, Abdullah Alsohibani, Ruba Alayed, et al.
Seizure|May 5, 2019
The landscape of early infantile epileptic encephalopathy in a consanguineous populationMarwan Nashabat, Xena S Al Qahtani, Salwa Almakdob, et al.
Frontiers in Pediatrics|March 8, 2021
Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 PandemicAhmed K Bamaga, Fouad Alghamdi, Nahla Alshaikh, et al.
American Journal of Medical Genetics. Part A|July 26, 2017
Congenital disorders of glycosylation: The Saudi experienceSarah Alsubhi, Amal Alhashem, Eissa Faqeih, et al.
Brain Communications|September 24, 2021
Homozygous missense <i>WIPI2</i> variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease courseReza Maroofian, Andrea Gubas, Rauan Kaiyrzhanov, et al.
Journal of Medical Genetics|August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Seizure|March 3, 2024
Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statementFahad A Bashiri, Khalid Hundallah, Raidah Al-Baradie, et al.
Journal of Child Neurology|December 1, 2025
Clinical and Genetic Spectrum of <i>SCN8A</i>-Related Disorders: A Retrospective Study From the Gulf RegionOsama Muthaffar, Mashael Alsubhan, Ali Mir, et al.
Pediatric Neurology|July 16, 2022
Hereditary Hyperekplexia in Saudi ArabiaAmal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, et al.
Pageof 3