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Page 1
Opsoclonus myoclonus induced by lamotrigine toxicity.
Zouari R, Bouchaala W, Nsir SB, Kamoun F, Triki C. Zouari R, et al. Among authors: kamoun f. Seizure. 2021 Oct;91:247-250. doi: 10.1016/j.seizure.2021.06.021. Epub 2021 Jun 29. Seizure. 2021. PMID: 34243055 Free article. No abstract available.
[Schimmelpenning-Feuerstein-Mims syndrome: a case report].
Bahloul E, Abid I, Masmoudi A, Makni S, Kamoun F, Boudawara T, Triki C, Turki H. Bahloul E, et al. Among authors: kamoun f. Arch Pediatr. 2015 Nov;22(11):1157-62. doi: 10.1016/j.arcped.2015.07.013. Epub 2015 Aug 29. Arch Pediatr. 2015. PMID: 26320679 French.
A Novel Mutation in the MAP7D3 Gene in Two Siblings with Severe Intellectual Disability and Autistic Traits: Concurrent Assessment of BDNF Functional Polymorphism, X-Inactivation and Oxidative Stress to Explain Disease Severity.
Kharrat M, Issa AB, Tlili A, Jallouli O, Alila-Fersi O, Maalej M, Chouchen J, Ghouylia Y, Kamoun F, Triki C, Fakhfakh F. Kharrat M, et al. Among authors: kamoun f. J Mol Neurosci. 2023 Oct;73(9-10):853-864. doi: 10.1007/s12031-023-02163-6. Epub 2023 Oct 10. J Mol Neurosci. 2023. PMID: 37817054
[Unilateral to bilateral pleurisy: Pleural tuberculosis?].
Ben Ameur S, Smaoui S, Kamoun F, Chabchoub I, Kamoun T, Messaadi F, Aloulou H, Hachicha M. Ben Ameur S, et al. Among authors: kamoun f. Arch Pediatr. 2016 Apr;23(4):385-8. doi: 10.1016/j.arcped.2016.01.014. Epub 2016 Feb 26. Arch Pediatr. 2016. PMID: 26922570 French.
MRI features in 17 patients with l2 hydroxyglutaric aciduria.
Fourati H, Ellouze E, Ahmadi M, Chaari D, Kamoun F, Hsairi I, Triki C, Mnif Z. Fourati H, et al. Among authors: kamoun f. Eur J Radiol Open. 2016 Sep 27;3:245-250. doi: 10.1016/j.ejro.2016.09.001. eCollection 2016. Eur J Radiol Open. 2016. PMID: 27709120 Free PMC article.
Knowledge and attitudes toward epilepsy among people in Sfax region, Tunisia.
Charfi Triki C, Mguidich T, Bouchaala W, Ben Ncir S, Chaari H, Fourati E, Ketata S, Kallel R, Kamoun F. Charfi Triki C, et al. Among authors: kamoun f. Epilepsy Behav. 2021 Sep;122:108151. doi: 10.1016/j.yebeh.2021.108151. Epub 2021 Jun 30. Epilepsy Behav. 2021. PMID: 34217034
Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy.
Ben Said M, Jallouli O, Ben Aissa A, Souissi A, Kamoun F, Fakhfakh F, Masmoudi S, Ben Ayed I, Charfi Triki C. Ben Said M, et al. Among authors: kamoun f. Epilepsia Open. 2024 Oct;9(5):1697-1709. doi: 10.1002/epi4.12848. Epub 2024 Jul 25. Epilepsia Open. 2024. PMID: 37867425 Free PMC article.
68 results