Salah A. Elmalik
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 11 publications
Electrophysiology of ataxia-telangiectasia-like disorder 1.
Journal: Sudanese journal of paediatrics
Published: December 20, 2020
Descriptive Patterns of Deafness Among Pre-School Saudi Children Aged Two to Five Years Visiting Neurology Clinic From 2012 to 2017.
Journal: Cureus
Published: November 16, 2020
Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15).
Journal: BMC neurology
Published: February 05, 2020
Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report.
Journal: BMC neurology
Published: May 17, 2018
SLC25A22 is a novel gene for migrating partial seizures in infancy.
Journal: Annals of neurology
Published: March 06, 2014
Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulation.
Journal: The British journal of ophthalmology
Published: February 14, 2014
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.
Journal: PloS one
Published: May 11, 2013
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.
Journal: American journal of human genetics
Published: June 28, 2012
A newly recognized autosomal recessive syndrome affecting neurologic function and vision.
Journal: American journal of medical genetics. Part A
Published: March 31, 2012
The neurology of carbonic anhydrase type II deficiency syndrome.
Journal: Brain : a journal of neurology
Published: November 29, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026