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De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.
Cell Rep. 2014 Oct 9;9(1):16-23. doi: 10.1016/j.celrep.2014.08.068. Epub 2014 Oct 2.
Cell Rep. 2014.
PMID: 25284784
Free PMC article.
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy.
Novarino G, El-Fishawy P, Kayserili H, Meguid NA, Scott EM, Schroth J, Silhavy JL, Kara M, Khalil RO, Ben-Omran T, Ercan-Sencicek AG, Hashish AF, Sanders SJ, Gupta AR, Hashem HS, Matern D, Gabriel S, Sweetman L, Rahimi Y, Harris RA, State MW, Gleeson JG.
Novarino G, et al. Among authors: khalil ro.
Science. 2012 Oct 19;338(6105):394-7. doi: 10.1126/science.1224631. Epub 2012 Sep 6.
Science. 2012.
PMID: 22956686
Free PMC article.
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A study of blood serotonin and serotonin transporter promoter variant (5-HTTLPR) polymorphism in Egyptian autistic children.
Meguid NA, Gebril OH, Khalil RO.
Meguid NA, et al. Among authors: khalil ro.
Adv Biomed Res. 2015 May 11;4:94. doi: 10.4103/2277-9175.156658. eCollection 2015.
Adv Biomed Res. 2015.
PMID: 26015920
Free PMC article.
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Role of polyunsaturated fatty acids in the management of Egyptian children with autism.
Meguid NA, Atta HM, Gouda AS, Khalil RO.
Meguid NA, et al. Among authors: khalil ro.
Clin Biochem. 2008 Sep;41(13):1044-8. doi: 10.1016/j.clinbiochem.2008.05.013. Epub 2008 Jun 12.
Clin Biochem. 2008.
PMID: 18582451
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The Digital Era Heralds a Paradigm Shift in Dentistry: A Cross-Sectional Study.
Suganna M, Nayakar RP, Alshaya AA, Khalil RO, Alkhunaizi ST, Kayello KT, Alnassar LA.
Suganna M, et al. Among authors: khalil ro.
Cureus. 2024 Jan 31;16(1):e53300. doi: 10.7759/cureus.53300. eCollection 2024 Jan.
Cureus. 2024.
PMID: 38435915
Free PMC article.
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