TitleAuthorPublication DatePublisherType
    Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1.  Zayed, Hatem; El Khayat, Hamed; Tomoum, Hoda; Khalifa, Ola; Siddiq, Ehab; ... more authors 2019SpringerArticle
    Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I  Mosaeilhy, Ahmed; Mohamed, Magdy M; C, George Priya Doss; El Abd, Heba S A; Gamal, Radwa; ... more authors 2017Springer USArticle
    Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.  Zaki, Osama K; Priya Doss C, George; Ali, Salsabil A; Murad, Ghadeer G; Elashi, Shaima A; ... more authors 2017Oxford University Press (OUP)Article
    Investigating the structural impacts of a novel missense variant identified with whole exome sequencing in an Egyptian patient with propionic acidemia  Ibrahim, Ali Zaki; Thirumal Kumar, D; Abunada, Taghreed; Younes, Salma; George Priya Doss, C; ... more authors 2020ElsevierArticle
    Novel mutation in an Egyptian patient with infantile Canavan disease.  Zaki, Osama K; El Abd, Heba S; Mohamed, Shaimaa A; Zayed, Hatem2016Springer Verlag (Germany)Article
    Two patients with Canavan disease and structural modeling of a novel mutation.  Zaki, Osama K; Krishnamoorthy, Navaneethakrishnan; El Abd, Heba S; Harche, Soumaya A; Mattar, Reem A; ... more authors 2017Springer USArticle