Zayed H - Search Results

1

Investigating the structural impacts of a novel missense variant identified with whole exome sequencing in an Egyptian patient with propionic acidemia.

Ibrahim AZ, Thirumal Kumar D, Abunada T, Younes S, George Priya Doss C, Zaki OK, Zayed H. Ibrahim AZ, et al. Among authors: zayed h. Mol Genet Metab Rep. 2020 Sep 17;25:100645. doi: 10.1016/j.ymgmr.2020.100645. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 32995289 Free PMC article.

2

Propionic acidemia in the Arab World.

Zayed H. Zayed H. Gene. 2015 Jun 15;564(2):119-24. doi: 10.1016/j.gene.2015.04.019. Epub 2015 Apr 9. Gene. 2015. PMID: 25865301 Review.

3

Novel mutation in an Egyptian patient with infantile Canavan disease.

Zaki OK, El Abd HS, Mohamed SA, Zayed H. Zaki OK, et al. Among authors: zayed h. Metab Brain Dis. 2016 Jun;31(3):573-7. doi: 10.1007/s11011-015-9772-z. Epub 2015 Nov 28. Metab Brain Dis. 2016. PMID: 26613958

4

Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene.

Moseilhy A, Hassan MM, El Abd HS, Mohammad SA, El Bekay R, Abdel-Motal UM, Ouhtit A, Zaki OK, Zayed H. Moseilhy A, et al. Among authors: zayed h. Metab Brain Dis. 2017 Feb;32(1):35-40. doi: 10.1007/s11011-016-9879-x. Epub 2016 Aug 1. Metab Brain Dis. 2017. PMID: 27476540

5

Two patients with Canavan disease and structural modeling of a novel mutation.

Zaki OK, Krishnamoorthy N, El Abd HS, Harche SA, Mattar RA, Al Disi RS, Nofal MY, El Bekay R, Ahmed KA, George Priya Doss C, Zayed H. Zaki OK, et al. Among authors: zayed h. Metab Brain Dis. 2017 Feb;32(1):171-177. doi: 10.1007/s11011-016-9896-9. Epub 2016 Aug 17. Metab Brain Dis. 2017. PMID: 27531131

6

Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation.

Ali SK, Sneha P, Priyadharshini Christy J, Zayed H, George Priya Doss C. Ali SK, et al. Among authors: zayed h. J Biomol Struct Dyn. 2017 Sep;35(12):2714-2724. doi: 10.1080/07391102.2016.1229634. Epub 2016 Sep 27. J Biomol Struct Dyn. 2017. PMID: 27677677

7

Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I.

Mosaeilhy A, Mohamed MM, C GPD, El Abd HSA, Gamal R, Zaki OK, Zayed H. Mosaeilhy A, et al. Among authors: zayed h. Metab Brain Dis. 2017 Oct;32(5):1417-1426. doi: 10.1007/s11011-017-0006-4. Epub 2017 Apr 7. Metab Brain Dis. 2017. PMID: 28389991

8

Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.

Zaki OK, Priya Doss C G, Ali SA, Murad GG, Elashi SA, Ebnou MSA, Kumar D T, Khalifa O, Gamal R, El Abd HSA, Nasr BN, Zayed H. Zaki OK, et al. Among authors: zayed h. Hum Mol Genet. 2017 Aug 15;26(16):3105-3115. doi: 10.1093/hmg/ddx195. Hum Mol Genet. 2017. PMID: 28535199

9

Comparative computational assessment of the pathogenicity of mutations in the Aspartoacylase enzyme.

George Priya Doss C, Zayed H. George Priya Doss C, et al. Among authors: zayed h. Metab Brain Dis. 2017 Dec;32(6):2105-2118. doi: 10.1007/s11011-017-0090-5. Epub 2017 Sep 6. Metab Brain Dis. 2017. PMID: 28879565

10

A profound computational study to prioritize the disease-causing mutations in PRPS1 gene.

Agrahari AK, Sneha P, George Priya Doss C, Siva R, Zayed H. Agrahari AK, et al. Among authors: zayed h. Metab Brain Dis. 2018 Apr;33(2):589-600. doi: 10.1007/s11011-017-0121-2. Epub 2017 Oct 18. Metab Brain Dis. 2018. PMID: 29047041

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