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Journal of Child Neurology|July 24, 2014
MEGDEL Syndrome in a Child From Palestine: Report of a Novel Mutation in SERAC1 GeneImad M Dweikat, Samer Abdelrazeq, Suhail Ayesh, et al.
BMC Medical Genomics|July 2, 2025
Molecular characterization, clinical phenotype, and neurological outcome of twelve Palestinian children with beta-ketothiolase deficiency: report of two novel variants in the ACAT1 geneImad M Dweikat, Hamza A Abdul-Hafez, Alaa Zayed, et al.
Brain & Development|July 17, 2010
Propionic acidemia mimicking diabetic ketoacidosisImad M Dweikat, Enas N Naser, Abdulsalam I Abu Libdeh, et al.
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