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Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases.
Mol Genet Genomic Med. 2018 Nov;6(6):1041-1052. doi: 10.1002/mgg3.480. Epub 2018 Oct 7.
Mol Genet Genomic Med. 2018.
PMID: 30293248
Free PMC article.
Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation.
Corbani S, Chouery E, Fayyad J, Fawaz A, El Tourjuman O, Badens C, Lacoste C, Delague V, Megarbane A.
Corbani S, et al. Among authors: el tourjuman o.
J Intellect Disabil Res. 2012 Apr;56(4):415-20. doi: 10.1111/j.1365-2788.2011.01479.x. Epub 2011 Sep 29.
J Intellect Disabil Res. 2012.
PMID: 21954873
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Hyperventilation-induced high-amplitude rhythmic slowing: A mimicker of absence seizures in children.
Nasreddine W, Fakhredin M, Makke Y, Hmaimess G, Sabbagh S, Beaini S, El Tourjuman O, Beydoun A.
Nasreddine W, et al. Among authors: el tourjuman o.
Epilepsy Behav. 2020 Feb;103(Pt A):106510. doi: 10.1016/j.yebeh.2019.106510. Epub 2019 Oct 20.
Epilepsy Behav. 2020.
PMID: 31645312
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When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospective Trial.
Hourani R, Nasreddine W, Dirani M, Hmaimess G, Sabbagh S, El Tourjuman O, Wazne J, Toufaili H, AlArab N, El Dassouki M, Beydoun A.
Hourani R, et al. Among authors: el tourjuman o.
AJNR Am J Neuroradiol. 2021 Sep;42(9):1695-1701. doi: 10.3174/ajnr.A7193. Epub 2021 Jul 8.
AJNR Am J Neuroradiol. 2021.
PMID: 34244128
Free PMC article.
Clinical Trial.
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[Bilateral frontal polymicrogyria and Ehlers-Danlos syndrome].
Ezzeddine H, Sabouraud P, Eschard C, El Tourjuman O, Bednarek N, Motte J.
Ezzeddine H, et al. Among authors: el tourjuman o.
Arch Pediatr. 2005 Feb;12(2):173-5. doi: 10.1016/j.arcped.2004.11.021.
Arch Pediatr. 2005.
PMID: 15694543
French.
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