العنوان | المؤلف | تاريخ النشر | الناشر | النوع |
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; Mohammad, Shaimaa A; Gamal, Radwa; Shi, Zumin; Mosailhy, Ahmed; Zaki, Osama K... more authors ... less authors | 2019 | Springer | Article |
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; Zaki, Osama K; Zayed, Hatem... more authors ... less authors | 2017 | Springer US | Article |
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; Ebnou, Maryam S A; Kumar D, Thirumal; Khalifa, Ola; Gamal, Radwa; El Abd, Heba S A; Nasr, Bilal N; Zayed, Hatem... more authors ... less authors | 2017 | Oxford 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; Zaki, Osama K; Zayed, Hatem... more authors ... less authors | 2020 | Elsevier | Article |
Novel mutation in an Egyptian patient with infantile Canavan disease.
| Zaki, Osama K; El Abd, Heba S; Mohamed, Shaimaa A; Zayed, Hatem | 2016 | Springer 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; Al Disi, Rana S; Nofal, Mariam Y; El Bekay, Rajaa; Ahmed, Khalid A; George Priya Doss, C; Zayed, Hatem... more authors ... less authors | 2017 | Springer US | Article |