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Saudi Medical Journal|January 1, 2015
Sirenomelia and severe caudal regression syndromeMohammed Z Seidahmed, Omer B Abdelbasit, Khalid A Alhussein, et al.
Saudi Medical Journal|March 15, 2006
Outcome of stroke in Saudi childrenMustafa A Salih, Abdel-Galil M Abdel-Gader, Ahmed A Al-Jarallah, et al.
Human Molecular Genetics|February 19, 2013
Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesisSalma Awad, Mohammed S Al-Dosari, Nadya Al-Yacoub, et al.
Human Genetics|April 24, 2016
A null mutation in TNIK defines a novel locus for intellectual disabilityShams Anazi, Hanan E Shamseldin, Dhekra AlNaqeb, et al.
Movement Disorders Clinical Practice|February 5, 2019
Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35Cecilia Marelli, Mustafa A Salih, Karine Nguyen, et al.
Neurogenetics|February 14, 2009
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's diseaseCécile Cazeneuve, Channkanira Sân, Salah A Ibrahim, et al.
The British Journal of Ophthalmology|February 14, 2014
Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulationArif O Khan, Abdulmajeed AlDrees, Salah A Elmalik, et al.
Ophthalmology|December 2, 2008
Ophthalmic features of Joubert syndromeArif O Khan, Darren T Oystreck, Mohamed Z Seidahmed, et al.
Neurosciences (Riyadh, Saudi Arabia)|February 2, 2021
Neurodevelopmental and epilepsy outcomes of patients with infantile spasms treated in a tertiary care centerFahad A Bashiri, Matar A Al-Sehemi, Muddathir H Hamad, et al.
BMC Medical Genetics|September 23, 2010
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlationKhaled K Abu-Amero, Ali M Hellani, Mustafa A Salih, et al.
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