El-Kotoury A - Search Results

1

Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I.

Abdel-Salam GM, Abdel-Hamid MS, Issa M, Magdy A, El-Kotoury A, Amr K. Abdel-Salam GM, et al. Among authors: el kotoury a. Am J Med Genet A. 2012 Jun;158A(6):1455-61. doi: 10.1002/ajmg.a.35356. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581640

2

Growth charts of Egyptian children with Down syndrome (0-36 months).

Meguid NA, El-Kotoury AI, Abdel-Salam GM, El-Ruby MO, Afifi HH. Meguid NA, et al. Among authors: el kotoury ai. East Mediterr Health J. 2004 Jan-Mar;10(1-2):106-15. East Mediterr Health J. 2004. PMID: 16201715 Free article.

3

The most encountered groups of genetic disorders in Giza Governorate, Egypt.

Afifi HH, El-Ruby MO, El-Bassyouni HT, Ismail SI, Aglan MS, El-Harouni AA, Mazen IM, Zaki MS, Bassiouni RI, Hosny LA, El-Kamah GY, El-Kotoury AI, Ashour AM, Abdel-Salam GM, El-Gammal MA, Hamed K, Kamal RM, El-Nekhely I, Temtamy SA. Afifi HH, et al. Among authors: el kotoury ai. Bratisl Lek Listy. 2010;111(2):62-9. Bratisl Lek Listy. 2010. PMID: 20429316

4

Mutational analysis of the PTPN11 gene in Egyptian patients with Noonan syndrome.

Essawi ML, Ismail MF, Afifi HH, Kobesiy MM, El Kotoury A, Barakat MM. Essawi ML, et al. Among authors: el kotoury a. J Formos Med Assoc. 2013 Nov;112(11):707-12. doi: 10.1016/j.jfma.2012.06.002. Epub 2012 Aug 1. J Formos Med Assoc. 2013. PMID: 24183200 Free article.

5

Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt.

Eid OM, Abdel Hady S, El-Kotoury A, Said KA, Rafat K, El-Bassyouni HT. Eid OM, et al. Among authors: el kotoury a. Ophthalmic Genet. 2017 Sep-Oct;38(5):418-421. doi: 10.1080/13816810.2016.1247460. Epub 2017 Jan 20. Ophthalmic Genet. 2017. PMID: 28107085

6

Prevalence of Congenital Ocular Anomalies among Children with Genetic Disorders: An Egyptian Study.

Tomairek RH, Amin MM, Raafat K, Abdel Hady S, Elkotoury A. Tomairek RH, et al. Semin Ophthalmol. 2018;33(5):613-619. doi: 10.1080/08820538.2017.1375124. Epub 2017 Oct 9. Semin Ophthalmol. 2018. PMID: 28991511

7

Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development.

Tantawy S, Mazen I, Soliman H, Anwar G, Atef A, El-Gammal M, El-Kotoury A, Mekkawy M, Torky A, Rudolf A, Schrumpf P, Grüters A, Krude H, Dumargne MC, Astudillo R, Bashamboo A, Biebermann H, Köhler B. Tantawy S, et al. Among authors: el kotoury a. Eur J Endocrinol. 2014 Apr 10;170(5):759-67. doi: 10.1530/EJE-13-0965. Print 2014 May. Eur J Endocrinol. 2014. PMID: 24591553

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