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Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 15, 2010
Congenital myasthenic syndrome due to homozygous CHRNE mutations: report of patients in ArabiaMustafa A Salih, Darren T Oystreck, Yasser H Al-Faky, et al.
American Journal of Medical Genetics. Part A|December 20, 2024
Sodium Oxybate-Treated Familial Myoclonus-Dystonia Syndrome Due to Novel SGCE VariantMalak Ali Alghamdi, Muddathir H Hamad, Isra Alghamdi, et al.
Saudi Medical Journal|March 15, 2006
Cardiac diseases as a risk factor for stroke in Saudi childrenMustafa A Salih, Abdullah S Al-Jarallah, Abdel-Galil M Abdel-Gader, et al.
Ophthalmic Genetics|February 15, 2013
Ophthalmologic observations in a patient with partial mosaic trisomy 8Khaled K Abu-Amero, Altaf A Kondkar, Mustafa A Salih, et al.
American Journal of Medical Genetics. Part A|May 2, 2013
A newly recognized autosomal recessive syndrome affecting neurologic function and visionMustafa A Salih, Andreas Tzschach, Darren T Oystreck, et al.
BMC Neurology|October 30, 2012
A novel syndrome of lethal familial hyperekplexia associated with brain malformationMohammed Zein Seidahmed, Mustafa A Salih, Omer B Abdulbasit, et al.
Neurogenetics|April 15, 2019
Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556Edmund S Cauley, Ahlam Hamed, Inaam N Mohamed, et al.
BMC Neurology|February 19, 2021
A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case reportAshraf Yahia, Zhefan Stephen Chen, Ammar E Ahmed, et al.
Brain : a Journal of Neurology|September 10, 2010
Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxiaMirna Assoum, Mustafa A Salih, Nathalie Drouot, et al.
Saudi Medical Journal|March 15, 2006
Congenital and genetic cerebrovascular anomalies as risk factors for stroke in Saudi childrenMustafa A Salih, Waleed R Murshid, Jihad N Zahraa, et al.
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