Osama K. Zaki
Cairo, C, Egypt
Last Updated: 09/26/2026
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Found 15 publications
Interaction between apolipoprotein E genotyping, serum inflammatory biomarkers and cognitive functions in Egyptian elderly.
Journal: The Egyptian journal of immunology
Published: June 20, 2021
Investigating the structural impacts of a novel missense variant identified with whole exome sequencing in an Egyptian patient with propionic acidemia.
Journal: Molecular genetics and metabolism reports
Published: August 03, 2020
Genotype-phenotype correlation of 33 patients with maple syrup urine disease.
Journal: American journal of medical genetics. Part A
Published: February 15, 2020
Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1.
Journal: Metabolic brain disease
Published: February 08, 2019
Effect of Estrogen Receptor- Alpha Gene Polymorphism (IVS1-397 T>C) on Microvascular Complications of Type 1 Diabetes Mellitus.
Journal: Current diabetes reviews
Published: January 01, 2019
Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.
Journal: Human molecular genetics
Published: April 28, 2017
Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I.
Journal: Metabolic brain disease
Published: February 07, 2017
Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study.
Journal: Orphanet journal of rare diseases
Published: November 30, 2016
Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene.
Journal: Metabolic brain disease
Published: May 13, 2016
Two patients with Canavan disease and structural modeling of a novel mutation.
Journal: Metabolic brain disease
Published: May 12, 2016
The Use of Glycomacropeptide in Dietary Management of Phenylketonuria.
Journal: Journal of nutrition and metabolism
Published: January 01, 2016
Novel mutation in an Egyptian patient with infantile Canavan disease.
Journal: Metabolic brain disease
Published: October 03, 2015
Last Updated: 09/26/2026