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Brahim Tabarki

Showing results (11-20 of 99) with videos related to

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Saudi Medical Journal|October 6, 2016
Comparison of inhaled nebulised adrenaline with salbutamol in acute asthmaFaouzia Khaldi, Brahim Tabarki, Nejla Salem
Epilepsy Research and Treatment|October 1, 2013
Epileptic encephalopathies in childrenBrahim Tabarki, Giangennaro Coppola, Elaine Wirrell
Neurosciences (Riyadh, Saudi Arabia)|April 5, 2021
Unilateral Lennox-Gastaut syndrome associated with Klippel-Trénaunay syndromeBrahim Tabarki, Khaled Hundallah, Nabil Biary
Archives of Disease in Childhood|February 2, 2019
Distinct neuroimaging features of <i>DDHD2</i> gene-related spastic paraplegia, a mimicker of cerebral palsyFarah Thabet, Kalthoum Tlili-Graiess, Brahim Tabarki
Pediatric Neurology|November 17, 2018
Embryopathy Associated With a Vitamin TherapyBrahim Tabarki, Amal AlHashem, Kalthoum Tlili-Graiess
Neurosciences (Riyadh, Saudi Arabia)|April 18, 2018
Neurometabolic disorders and congenital malformations of the central nervous systemAhmed Y BoAli, Majid Alfadhel, Brahim Tabarki
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 28, 2016
Severe early-onset epileptic encephalopathy due to mutations in the KCNA2 gene: Expansion of the genotypic and phenotypic spectrumKhaled Hundallah, Asma'a Alenizi, Amal AlHashem, et al.
Molecular Genetics and Metabolism|September 5, 2024
CIC variants and folinic acid-responsive seizuresMeshal Almutair, Farah Thabet, Khalid Hundallah, et al.
Experimental Biology and Medicine (Maywood, N.J.)|November 23, 2014
The fragile site WWOX gene and the developing brainBrahim Tabarki, Fuad Al Mutairi, Amal Al Hashem
Journal of Child Neurology|October 8, 2013
A wide clinical phenotype spectrum in patients with ATP1A2 mutationsBashaer Al-Bulushi, Amal Al-Hashem, Brahim Tabarki
Pageof 10

Showing results (11-20 of 99) with videos related to

Sort By:
Pageof 10
Saudi Medical Journal|October 6, 2016
Comparison of inhaled nebulised adrenaline with salbutamol in acute asthmaFaouzia Khaldi, Brahim Tabarki, Nejla Salem
Epilepsy Research and Treatment|October 1, 2013
Epileptic encephalopathies in childrenBrahim Tabarki, Giangennaro Coppola, Elaine Wirrell
Neurosciences (Riyadh, Saudi Arabia)|April 5, 2021
Unilateral Lennox-Gastaut syndrome associated with Klippel-Trénaunay syndromeBrahim Tabarki, Khaled Hundallah, Nabil Biary
Archives of Disease in Childhood|February 2, 2019
Distinct neuroimaging features of <i>DDHD2</i> gene-related spastic paraplegia, a mimicker of cerebral palsyFarah Thabet, Kalthoum Tlili-Graiess, Brahim Tabarki
Pediatric Neurology|November 17, 2018
Embryopathy Associated With a Vitamin TherapyBrahim Tabarki, Amal AlHashem, Kalthoum Tlili-Graiess
Neurosciences (Riyadh, Saudi Arabia)|April 18, 2018
Neurometabolic disorders and congenital malformations of the central nervous systemAhmed Y BoAli, Majid Alfadhel, Brahim Tabarki
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 28, 2016
Severe early-onset epileptic encephalopathy due to mutations in the KCNA2 gene: Expansion of the genotypic and phenotypic spectrumKhaled Hundallah, Asma'a Alenizi, Amal AlHashem, et al.
Molecular Genetics and Metabolism|September 5, 2024
CIC variants and folinic acid-responsive seizuresMeshal Almutair, Farah Thabet, Khalid Hundallah, et al.
Experimental Biology and Medicine (Maywood, N.J.)|November 23, 2014
The fragile site WWOX gene and the developing brainBrahim Tabarki, Fuad Al Mutairi, Amal Al Hashem
Journal of Child Neurology|October 8, 2013
A wide clinical phenotype spectrum in patients with ATP1A2 mutationsBashaer Al-Bulushi, Amal Al-Hashem, Brahim Tabarki
Pageof 10