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Brahim Tabarki

Showing results (41-50 of 99) with videos related to

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Child Neurology Open|January 27, 2018
PRUNE Syndrome Is a New Neurodevelopmental Disorder: Report and ReviewMajid Alfadhel, Marwan Nashabat, Khalid Hundallah, et al.
Archives of Disease in Childhood. Education and Practice Edition|September 9, 2020
Problem-solving in clinical practice: breathing difficulty and muscle weakness following allogeneic haematopoietic stem cell transplantationBashaer Albulushi, Farah Thabet, Saad Alshahwan, et al.
Molecular Genetics and Metabolism|February 11, 2026
Exploring the clinical, neuroimaging, and genetic spectrum of PLPBP deficiency: multicenter case series and systematic reviewHanin Alsini, Ali Al-Otaibi, Imran Ali Khan, et al.
Pediatrics|November 14, 2012
Pyridoxine-dependent epilepsy with elevated urinary α-amino adipic semialdehyde in molybdenum cofactor deficiencyEduard Alexander Struys, Benjamin Nota, Abdellatif Bakkali, et al.
Brain & Development|July 27, 2012
Acute necrotizing encephalopathy associated with enterovirus infectionBrahim Tabarki, Farah Thabet, Shatha Al Shafi, et al.
Neurogenetics|January 19, 2024
Bi-allelic variants in HCRT cause autosomal recessive narcolepsyWejdan Hakami, Farah Thabet, Amal Alhashem, et al.
Pediatric Neurology|April 29, 2017
Recessive AFG3L2 Mutation Causes Progressive Microcephaly, Early Onset Seizures, Spasticity, and Basal Ganglia InvolvementAlaa Eskandrani, Amal AlHashem, El-Sayed Ali, et al.
Journal of Child Neurology|July 31, 2003
Acute transverse myelitis in children: clinical course and prognostic factorsPierre Defresne, Henri Hollenberg, Béatrice Husson, et al.
Human Genetics|November 9, 2021
Mitochondrial "dysmorphology" in variant classificationHanan E Shamseldin, Amal Alhashem, Brahim Tabarki, et al.
Neurology. Genetics|July 13, 2022
A Biallelic Variant in <i>FRA10AC1</i> Is Associated With Neurodevelopmental Disorder and Growth RetardationNorah Alsaleh, Amal Alhashem, Brahim Tabarki, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
Child Neurology Open|January 27, 2018
PRUNE Syndrome Is a New Neurodevelopmental Disorder: Report and ReviewMajid Alfadhel, Marwan Nashabat, Khalid Hundallah, et al.
Archives of Disease in Childhood. Education and Practice Edition|September 9, 2020
Problem-solving in clinical practice: breathing difficulty and muscle weakness following allogeneic haematopoietic stem cell transplantationBashaer Albulushi, Farah Thabet, Saad Alshahwan, et al.
Molecular Genetics and Metabolism|February 11, 2026
Exploring the clinical, neuroimaging, and genetic spectrum of PLPBP deficiency: multicenter case series and systematic reviewHanin Alsini, Ali Al-Otaibi, Imran Ali Khan, et al.
Pediatrics|November 14, 2012
Pyridoxine-dependent epilepsy with elevated urinary α-amino adipic semialdehyde in molybdenum cofactor deficiencyEduard Alexander Struys, Benjamin Nota, Abdellatif Bakkali, et al.
Brain & Development|July 27, 2012
Acute necrotizing encephalopathy associated with enterovirus infectionBrahim Tabarki, Farah Thabet, Shatha Al Shafi, et al.
Neurogenetics|January 19, 2024
Bi-allelic variants in HCRT cause autosomal recessive narcolepsyWejdan Hakami, Farah Thabet, Amal Alhashem, et al.
Pediatric Neurology|April 29, 2017
Recessive AFG3L2 Mutation Causes Progressive Microcephaly, Early Onset Seizures, Spasticity, and Basal Ganglia InvolvementAlaa Eskandrani, Amal AlHashem, El-Sayed Ali, et al.
Journal of Child Neurology|July 31, 2003
Acute transverse myelitis in children: clinical course and prognostic factorsPierre Defresne, Henri Hollenberg, Béatrice Husson, et al.
Human Genetics|November 9, 2021
Mitochondrial "dysmorphology" in variant classificationHanan E Shamseldin, Amal Alhashem, Brahim Tabarki, et al.
Neurology. Genetics|July 13, 2022
A Biallelic Variant in <i>FRA10AC1</i> Is Associated With Neurodevelopmental Disorder and Growth RetardationNorah Alsaleh, Amal Alhashem, Brahim Tabarki, et al.
Pageof 10