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Brahim Tabarki

Showing results (61-70 of 99) with videos related to

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Neurology|December 28, 2012
Biotin-responsive basal ganglia disease revisited: clinical, radiologic, and genetic findingsBrahim Tabarki, Shatha Al-Shafi, Saad Al-Shahwan, et al.
Acta Epileptologica|May 9, 2025
Safety and effectiveness of vagus nerve stimulation in patients with drug-resistant epilepsy: a single center experienceEbtehal Alwazna, Jamal Abdullah, Hanin Alsini, et al.
Clinical Genetics|February 22, 2019
A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasiaZafer Yüksel, Florian Vogel, Amal M Alhashem, 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.
La Tunisie Medicale|February 28, 2004
[Cardiovascular manifestations of Kawasaki syndrome. Value of echocardiography in diagnosis and progression]Abdallah Mahdhaoui, Brahim Tabarki, Hatem Bouraoui, et al.
American Journal of Human Genetics|November 27, 2015
RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in HumansHanan Shamseldin, Anas M Alazami, Melanie Manning, et al.
Molecular Genetics and Metabolism Reports|June 4, 2026
POLG-related disorders: Clinical and molecular Spectrum in the Saudi populationFuad Al Mutairi, Faisal Joueidi, Ziyad A Al Mutairi, et al.
Annals of Neurology|September 1, 2017
Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictorsJuan Darío Ortigoza-Escobar, Majid Alfadhel, Marta Molero-Luis, 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.
Human Genetics|December 20, 2022
CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopmentDaphne J Smits, Jordy Dekker, Rachel Schot, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
Neurology|December 28, 2012
Biotin-responsive basal ganglia disease revisited: clinical, radiologic, and genetic findingsBrahim Tabarki, Shatha Al-Shafi, Saad Al-Shahwan, et al.
Acta Epileptologica|May 9, 2025
Safety and effectiveness of vagus nerve stimulation in patients with drug-resistant epilepsy: a single center experienceEbtehal Alwazna, Jamal Abdullah, Hanin Alsini, et al.
Clinical Genetics|February 22, 2019
A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasiaZafer Yüksel, Florian Vogel, Amal M Alhashem, 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.
La Tunisie Medicale|February 28, 2004
[Cardiovascular manifestations of Kawasaki syndrome. Value of echocardiography in diagnosis and progression]Abdallah Mahdhaoui, Brahim Tabarki, Hatem Bouraoui, et al.
American Journal of Human Genetics|November 27, 2015
RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in HumansHanan Shamseldin, Anas M Alazami, Melanie Manning, et al.
Molecular Genetics and Metabolism Reports|June 4, 2026
POLG-related disorders: Clinical and molecular Spectrum in the Saudi populationFuad Al Mutairi, Faisal Joueidi, Ziyad A Al Mutairi, et al.
Annals of Neurology|September 1, 2017
Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictorsJuan Darío Ortigoza-Escobar, Majid Alfadhel, Marta Molero-Luis, 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.
Human Genetics|December 20, 2022
CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopmentDaphne J Smits, Jordy Dekker, Rachel Schot, et al.
Pageof 10