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Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.
Hassan FA, El-Mougy F, Sharaf SA, Mandour I, Morgan MF, Selim LA, Hassan SA, Salem F, Oraby A, Girgis MY, Mahmoud IG, El-Badawy A, El-Nekhely I, Moharam N, Mehaney DA, Elmonem MA. Hassan FA, et al. Among authors: mandour i. J Med Screen. 2016 Sep;23(3):124-9. doi: 10.1177/0969141315618229. Epub 2016 Jan 20. J Med Screen. 2016. PMID: 26790708
Gene mutations in Wilson disease in Egyptian children: report on two novel mutations.
El-Mougy FA, Sharaf SA, Elsharkawy MM, Mandour IA, El-Essawy RA, Eldin AM, Helmy HM, Soliman DH, Selim LH, Sharafeldin HM, Mogahed EA, El-Karaksy HM. El-Mougy FA, et al. Among authors: mandour ia. Arab J Gastroenterol. 2014 Sep-Dec;15(3-4):114-8. doi: 10.1016/j.ajg.2014.10.005. Epub 2014 Nov 21. Arab J Gastroenterol. 2014. PMID: 25465132
13 results