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Plos One|October 21, 2014
Triple test screening for Down syndrome: an Egyptian-tailored studyHazem S Abou-Youssef, Manal M Kamal, Dina A MehaneyClinical Biochemistry|November 22, 2015
Association of chitotriosidase enzyme activity and genotype with the risk of nephropathy in type 2 diabetesMohamed A Elmonem, Hanan S Amin, Riham A El-Essawy, et al.Journal of Advanced Research|February 17, 2015
Profile of cystic fibrosis in a single referral center in EgyptMona M El-Falaki, Walaa A Shahin, Noussa R El-Basha, et al.Plos One|June 24, 2016
Serum Vitamin D and Vitamin D Receptor Gene Polymorphism in Mycosis Fungoides Patients: A Case Control StudyHoda Rasheed, Rehab A Hegazy, Heba I Gawdat, et al.Plos One|June 11, 2014
Analysis of oxidative stress status, catalase and catechol-O-methyltransferase polymorphisms in Egyptian vitiligo patientsDina A Mehaney, Hebatallah A Darwish, Rehab A Hegazy, et al.Journal of the Neurological Sciences|September 23, 2016
Interleukins 17 and 10 in a sample of Egyptian relapsing remitting multiple sclerosis patientsTarek Z Tawfik, Adel H Gad, Dina A Mehaney, et al.Cardiology in the Young|October 5, 2020
Genetic study of pediatric hypertrophic cardiomyopathy in EgyptRania K Darwish, Alireza Haghighi, Zeinab S Seliem, et al.Cardiology in the Young|May 26, 2021
Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian childrenDina A Mehaney, Alireza Haghighi, Amira K Embaby, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|January 7, 2023
Organic acidurias in Egyptian children: The urge for high-risk screeningDina A Mehaney, Zeinab S Seliem, Laila A Selim, et al.Indian Journal of Pediatrics|February 3, 2016
Lysosomal Storage Disorders in Egyptian ChildrenMohamed A Elmonem, Iman G Mahmoud, Dina A Mehaney, et al.Pageof 2