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Brahim Tabarki

Showing results (31-40 of 99) with videos related to

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Journal of Child Neurology|December 14, 2011
Further magnetic resonance imaging (MRI) brain delineation of 49,XXXXY syndromeBrahim Tabarki, Shatha Al Shafi, Nawal Al Adwani, et al.
Frontiers in Neurology|September 24, 2021
Editorial: Pediatric Neurometabolic DisordersBrahim Tabarki, Juan Dario Ortigoza-Escobar, Wang-Tso Lee, et al.
Pediatric Neurology|May 18, 2023
Acute Flaccid Myelitis in a Pediatric Patient With Coronavirus Disease 2019Farah Thabet, Abir Daya, Seifeddine Zayani, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 23, 2015
Treatment of biotin-responsive basal ganglia disease: Open comparative study between the combination of biotin plus thiamine versus thiamine aloneBrahim Tabarki, Majid Alfadhel, Saad AlShahwan, et al.
Brain & Development|July 10, 2022
Beyond the caudate nucleus: Early atypical neuroimaging findings in biotin-thiamine- responsive basal ganglia diseaseHanin Alsini, Aisha Alnozha, Zeeshan Asmat, et al.
American Journal of Medical Genetics. Part A|September 9, 2015
Severe CNS involvement in WWOX mutations: Description of five new casesBrahim Tabarki, Amal AlHashem, Saad AlShahwan, et al.
Frontiers in Neurology|March 22, 2021
Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and ManagementBrahim Tabarki, Wejdan Hakami, Nader Alkhuraish, et al.
Journal of Child Neurology|April 16, 2003
Familial spastic paraplegia as the presenting manifestation in patients with purine nucleoside phosphorylase deficiencyBrahim Tabarki, Moncef Yacoub, Kalthoum Tlili, et al.
European Journal of Pediatrics|April 20, 2006
ANCA-associated diffuse alveolar hemorrhage due to benzylthiouracilFarah Thabet, Rim Sghiri, Brahim Tabarki, et al.
Pediatric Neurology|November 28, 2018
Novel Homozygous Mutation of the AIMP1 Gene: A Milder Neuroimaging Phenotype With Preservation of the Deep White MatterAhmed BoAli, Kalthoum Tlili-Graiess, Amal AlHashem, et al.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
Journal of Child Neurology|December 14, 2011
Further magnetic resonance imaging (MRI) brain delineation of 49,XXXXY syndromeBrahim Tabarki, Shatha Al Shafi, Nawal Al Adwani, et al.
Frontiers in Neurology|September 24, 2021
Editorial: Pediatric Neurometabolic DisordersBrahim Tabarki, Juan Dario Ortigoza-Escobar, Wang-Tso Lee, et al.
Pediatric Neurology|May 18, 2023
Acute Flaccid Myelitis in a Pediatric Patient With Coronavirus Disease 2019Farah Thabet, Abir Daya, Seifeddine Zayani, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 23, 2015
Treatment of biotin-responsive basal ganglia disease: Open comparative study between the combination of biotin plus thiamine versus thiamine aloneBrahim Tabarki, Majid Alfadhel, Saad AlShahwan, et al.
Brain & Development|July 10, 2022
Beyond the caudate nucleus: Early atypical neuroimaging findings in biotin-thiamine- responsive basal ganglia diseaseHanin Alsini, Aisha Alnozha, Zeeshan Asmat, et al.
American Journal of Medical Genetics. Part A|September 9, 2015
Severe CNS involvement in WWOX mutations: Description of five new casesBrahim Tabarki, Amal AlHashem, Saad AlShahwan, et al.
Frontiers in Neurology|March 22, 2021
Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and ManagementBrahim Tabarki, Wejdan Hakami, Nader Alkhuraish, et al.
Journal of Child Neurology|April 16, 2003
Familial spastic paraplegia as the presenting manifestation in patients with purine nucleoside phosphorylase deficiencyBrahim Tabarki, Moncef Yacoub, Kalthoum Tlili, et al.
European Journal of Pediatrics|April 20, 2006
ANCA-associated diffuse alveolar hemorrhage due to benzylthiouracilFarah Thabet, Rim Sghiri, Brahim Tabarki, et al.
Pediatric Neurology|November 28, 2018
Novel Homozygous Mutation of the AIMP1 Gene: A Milder Neuroimaging Phenotype With Preservation of the Deep White MatterAhmed BoAli, Kalthoum Tlili-Graiess, Amal AlHashem, et al.
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