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Afnan Alhakeem

Showing results (1-10 of 5) with videos related to

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Neurosciences (Riyadh, Saudi Arabia)|September 26, 2014
Antiepileptic drugsAfnan Alhakeem, Brahim Tabarki
Brain & Development|June 14, 2018
Extending the use of stiripentol to SLC13A5-related epileptic encephalopathyAfnan Alhakeem, Faisal Alshibani, Brahim Tabarki
Pediatric Neurology|July 16, 2022
Hereditary Hyperekplexia in Saudi ArabiaAmal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2019
Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathyRené G Feichtinger, Bettina E Mucha, Holger Hengel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotoniaAlison M Muir, Jennifer F Gardner, Richard H van Jaarsveld, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Neurosciences (Riyadh, Saudi Arabia)|September 26, 2014
Antiepileptic drugsAfnan Alhakeem, Brahim Tabarki
Brain & Development|June 14, 2018
Extending the use of stiripentol to SLC13A5-related epileptic encephalopathyAfnan Alhakeem, Faisal Alshibani, Brahim Tabarki
Pediatric Neurology|July 16, 2022
Hereditary Hyperekplexia in Saudi ArabiaAmal Aldhilan, Afnan Alhakeem, Sumayah Al Hajjaj, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2019
Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathyRené G Feichtinger, Bettina E Mucha, Holger Hengel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotoniaAlison M Muir, Jennifer F Gardner, Richard H van Jaarsveld, et al.
Pageof 1