el-Awady M - Search Results

1

Haplotypes and mutations of the PAH locus in Egyptian families with PKU.

Effat L, Kuzmin A, Kasem N, Meguid NA, Kotb S, Eisensmith RC, Temtamy SA, Rushdi S, Woo S, el-Awady M. Effat L, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):259-62. doi: 10.1038/sj.ejhg.5200270. Eur J Hum Genet. 1999. PMID: 10196714

2

Molecular analysis of androgen resistance syndromes in Egyptian patients.

Essawi M, Gad YZ, el-Rouby O, Temtamy SA, Sabour YA, el-Awady MK. Essawi M, et al. Dis Markers. 1997 Apr;13(2):99-105. Dis Markers. 1997. PMID: 9160185

3

Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.

Effat LK, El-Harouni AA, Amr KS, El-Minisi TI, Abdel Meguid N, El-Awady M. Effat LK, et al. Dis Markers. 2000;16(3-4):125-9. doi: 10.1155/2000/437372. Dis Markers. 2000. PMID: 11381192 Free PMC article.

4

MTHFR genetic polymorphism as a risk factor in Egyptian mothers with Down syndrome children.

Meguid NA, Dardir AA, Khass M, Hossieny LE, Ezzat A, El Awady MK. Meguid NA, et al. Dis Markers. 2008;24(1):19-26. doi: 10.1155/2008/214027. Dis Markers. 2008. PMID: 18057532 Free PMC article.

5

Methylenetetrahydrofolate reductase gene polymorphisms and the risk of colorectal carcinoma in a sample of Egyptian individuals.

El Awady MK, Karim AM, Hanna LS, El Husseiny LA, El Sahar M, Menem HA, Meguid NA. El Awady MK, et al. Cancer Biomark. 2009;5(6):233-40. doi: 10.3233/CBM-2009-0108. Cancer Biomark. 2009. PMID: 20037199

6

Direct molecular analysis of the fragile X syndrome in a sample of Egyptian and German patients using non-radioactive PCR and Southern blot followed by chemiluminescent detection.

el-Aleem AA, Böhm I, Temtamy S, el-Awady M, Awadalla M, Schmidtke J, Stuhrmann M. el-Aleem AA, et al. Hum Genet. 1995 Nov;96(5):577-84. doi: 10.1007/BF00197414. Hum Genet. 1995. PMID: 8530006

7

Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot study.

Meguid NA, Ismail MF, El-Mahdy RS, Barakat MA, El-Awady MK. Meguid NA, et al. Acta Biochim Pol. 2014;61(2):259-63. Epub 2014 Jun 16. Acta Biochim Pol. 2014. PMID: 24936518

8

The milder phenotype of the dystrophin gene double deletions.

El-Harouni AA, Amr KS, Effat LK, Eassawi ML, Ismail S, Gad YZ, El-Awady MK. El-Harouni AA, et al. Acta Neurol Scand. 2003 Jun;107(6):400-4. doi: 10.1034/j.1600-0404.2003.00072.x. Acta Neurol Scand. 2003. PMID: 12757471

9

Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells.

El-Awady MK, Gad YZ, Wen Y, Eassawi M, Effat L, Amr KS, Ismail S, Christ GJ. El-Awady MK, et al. World J Urol. 2001 Aug;19(4):263-6. doi: 10.1007/s003450100217. World J Urol. 2001. PMID: 11550787

10

Polymorphism in variable number of tandem repeats of dopamine d4 gene is a genetic risk factor in attention deficit hyperactive egyptian children: pilot study.

Shahin O, Meguid NA, Raafat O, Dawood RM, Doss M, Bader El Din NG, El Awady MK. Shahin O, et al. Biomark Insights. 2015 May 5;10:33-8. doi: 10.4137/BMI.S18519. eCollection 2015. Biomark Insights. 2015. PMID: 25983551 Free PMC article.

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