el-Awady M - Search Results

1

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

2

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

3

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

4

Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism.

el-Awady MK, Temtamy SA, Salam MA, Gad YZ. el-Awady MK, et al. Hum Hered. 1987;37(1):36-40. doi: 10.1159/000153675. Hum Hered. 1987. PMID: 3557461

5

Deficient 5 alpha-reductase due to mutant enzyme with reduced affinity to steroid substrate.

el Awady MK, Salam MA, Temtamy SA. el Awady MK, et al. Enzyme. 1984;32(2):116-25. doi: 10.1159/000469461. Enzyme. 1984. PMID: 6333981

6

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

7

Assay for hepatitis C virus in peripheral blood mononuclear cells enhances sensitivity of diagnosis and monitoring of HCV-associated hepatitis.

El-Awady MK, Ismail SM, El-Sagheer M, Sabour YA, Amr KS, Zaki EA. El-Awady MK, et al. Clin Chim Acta. 1999 May;283(1-2):1-14. doi: 10.1016/s0009-8981(99)00007-8. Clin Chim Acta. 1999. PMID: 10404726 Clinical Trial.

8

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.

9

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.

10

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

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