Zayed H - Search Results

1

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

2

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

3

Structural modeling of p.V31F variant in the aspartoacylase gene.

Krishnamoorthy N, Zayed H. Krishnamoorthy N, et al. Among authors: zayed h. Metab Brain Dis. 2016 Jun;31(3):723-6. doi: 10.1007/s11011-016-9796-z. Epub 2016 Jan 21. Metab Brain Dis. 2016. PMID: 26797702

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

Structural Analysis of G1691S Variant in the Human Filamin B Gene Responsible for Larsen Syndrome: A Comparative Computational Approach.

P S, D KT, Tanwar H, R S, C GPD, Zayed H. P S, et al. Among authors: zayed h. J Cell Biochem. 2017 Jul;118(7):1900-1910. doi: 10.1002/jcb.25920. Epub 2017 Mar 27. J Cell Biochem. 2017. PMID: 28145583

7

Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.

P S, D TK, C GPD, R S, Zayed H. P S, et al. Among authors: zayed h. PLoS One. 2017 Apr 14;12(4):e0174953. doi: 10.1371/journal.pone.0174953. eCollection 2017. PLoS One. 2017. PMID: 28410371 Free PMC article.

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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