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Journal of Child Neurology
|
December 9, 2020
Identifying Clinical Clues in Children With Global Developmental Delay / Intellectual Disability With Abnormal Brain Magnetic Resonance Imaging (MRI)
Abdullah Alamri, Yaser I Aljadhai, Abdullah Alrashed, et al.
Frontiers in Pediatrics
|
January 30, 2025
Neuropsychiatric profile in tuberous sclerosis complex patients with epilepsy
Mahmoud Fawzi Osman, Faisal Hadid, Tawfeg Ben Omran, et al.
International Journal of Molecular Sciences
|
April 17, 2025
Novel <i>SCYL2</i> Mutations and Arthrogryposis Multiplex Congenita 4: Case Report and Review of the Literature
Khaled Zamel, Abdulrahman Ahmed Al-Subaiey, Mohamed Alsabbagh, et al.
Pediatric Neurology
|
April 6, 2021
Amelioration of Levetiracetam-Induced Behavioral Side Effects by Pyridoxine. A Randomized Double Blind Controlled Study
Adel Mahmoud, Sadia Tabassum, Shoaa Al Enazi, et al.
AJNR. American Journal of Neuroradiology
|
March 16, 2026
Aicardi-Goutières Syndrome: Insights from a Middle Eastern Case Series
Osamah Alwalid, Marwa Al Subhi, Ala Aldeen Al Serhan, et al.
International Journal of Molecular Sciences
|
June 26, 2025
The Complex Etiology of Epilepsy: Genetic Analysis and HLA Association in Patients in the Middle East
Abeer Fadda, Mohamed Alsabbagh, Dhanya Vasudeva, et al.
Epilepsy Research
|
February 26, 2026
EEG practices and discontinuation of anti-seizure medications in people with epilepsy: A cross-sectional survey in the Eastern Mediterranean region
Leen Alkalbani, Ruba Benini, Khaled Zamel, et al.
Epilepsy Research
|
May 8, 2022
Landscape of childhood epilepsies - A multi-ethnic population-based study
Ruba Benini, Nadine Asir, Ahmad Yasin, et al.
Case Reports in Genetics
|
December 29, 2025
Rare Presentation of Homozygous S<i>LC20A2</i> Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
Laila Baker, Faisal Hadid, Sara Salahaldeen Irshaidat, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Biallelic Loss-of-Function Variant in <i>MINPP1</i> Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder
Aljazi Al-Maraghi, Rulan Shaath, Katherine Ford, et al.
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Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Journal of Child Neurology
|
December 9, 2020
Identifying Clinical Clues in Children With Global Developmental Delay / Intellectual Disability With Abnormal Brain Magnetic Resonance Imaging (MRI)
Abdullah Alamri, Yaser I Aljadhai, Abdullah Alrashed, et al.
Frontiers in Pediatrics
|
January 30, 2025
Neuropsychiatric profile in tuberous sclerosis complex patients with epilepsy
Mahmoud Fawzi Osman, Faisal Hadid, Tawfeg Ben Omran, et al.
International Journal of Molecular Sciences
|
April 17, 2025
Novel <i>SCYL2</i> Mutations and Arthrogryposis Multiplex Congenita 4: Case Report and Review of the Literature
Khaled Zamel, Abdulrahman Ahmed Al-Subaiey, Mohamed Alsabbagh, et al.
Pediatric Neurology
|
April 6, 2021
Amelioration of Levetiracetam-Induced Behavioral Side Effects by Pyridoxine. A Randomized Double Blind Controlled Study
Adel Mahmoud, Sadia Tabassum, Shoaa Al Enazi, et al.
AJNR. American Journal of Neuroradiology
|
March 16, 2026
Aicardi-Goutières Syndrome: Insights from a Middle Eastern Case Series
Osamah Alwalid, Marwa Al Subhi, Ala Aldeen Al Serhan, et al.
International Journal of Molecular Sciences
|
June 26, 2025
The Complex Etiology of Epilepsy: Genetic Analysis and HLA Association in Patients in the Middle East
Abeer Fadda, Mohamed Alsabbagh, Dhanya Vasudeva, et al.
Epilepsy Research
|
February 26, 2026
EEG practices and discontinuation of anti-seizure medications in people with epilepsy: A cross-sectional survey in the Eastern Mediterranean region
Leen Alkalbani, Ruba Benini, Khaled Zamel, et al.
Epilepsy Research
|
May 8, 2022
Landscape of childhood epilepsies - A multi-ethnic population-based study
Ruba Benini, Nadine Asir, Ahmad Yasin, et al.
Case Reports in Genetics
|
December 29, 2025
Rare Presentation of Homozygous S<i>LC20A2</i> Mutations Causing Intra-Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
Laila Baker, Faisal Hadid, Sara Salahaldeen Irshaidat, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Biallelic Loss-of-Function Variant in <i>MINPP1</i> Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder
Aljazi Al-Maraghi, Rulan Shaath, Katherine Ford, et al.
Page
of 4