Ola A. Khalifa
Cairo, C, Egypt
Last Updated: 09/26/2026
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Found 18 publications
The effects of a self-learning package on mothers' knowledge and practices towards caring for their children with phenylketonuria.
Journal: Journal of medicine and life
Published: October 03, 2022
Genotype-phenotype correlation of 33 patients with maple syrup urine disease.
Journal: American journal of medical genetics. Part A
Published: February 15, 2020
Optic neuropathy in classical methylmalonic acidemia.
Journal: Ophthalmic genetics
Published: July 05, 2019
Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1.
Journal: Metabolic brain disease
Published: February 08, 2019
The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients.
Journal: Molecular genetics and metabolism reports
Published: November 29, 2017
Molecular autopsy in maternal-fetal medicine.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 17, 2017
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
Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
Journal: American journal of medical genetics. Part A
Published: July 02, 2016
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue.
Journal: Human genetics
Published: December 31, 2015
Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families.
Journal: International journal of dermatology
Published: October 21, 2015
Last Updated: 09/26/2026