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Page 1
Recurrent pneumococcal meningitis in children: Diagnostic dilemma.
Ben Belgacem H, Soyah N, Brahem D, Abdelbari M, Kebaili R, Tilouche S, Jaballah N, Tej A, Bouguila J, Boughamoura L. Ben Belgacem H, et al. Among authors: bouguila j. Tunis Med. 2024 Jul 5;102(7):377-378. Tunis Med. 2024. PMID: 38982959 No abstract available.
Effect of diabetes self-management education on health-related quality of life of Tunisian children with type1 diabetes mellitus and their parents: A randomized controlled trial.
Ben Abdesselem I, Kebaili R, Derbel K, Ben Said H, Boughammoura L, Rouatbi S, Bouguila J. Ben Abdesselem I, et al. Among authors: bouguila j. Tunis Med. 2024 Apr 5;102(4):205-211. doi: 10.62438/tunismed.v102i4.4846. Tunis Med. 2024. PMID: 38746959 Free PMC article. Clinical Trial. English.
Fulminant Encephalitis Caused by SARS-CoV-2 in a Two-Month-Old Infant.
Abdelbari M, Tilouche S, Hannachi S, Bouguila J, Hannachi N, Boughammoura L. Abdelbari M, et al. Among authors: bouguila j. Indian J Pediatr. 2023 Jan;90(1):101. doi: 10.1007/s12098-022-04404-9. Epub 2022 Nov 28. Indian J Pediatr. 2023. PMID: 36441385 Free PMC article. No abstract available.
Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
Alila OF, Rebai EM, Tabebi M, Tej A, Chamkha I, Tlili A, Bouguila J, Tilouche S, Soyah N, Boughamoura L, Fakhfakh F. Alila OF, et al. Among authors: bouguila j. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Jul;27(4):2873-80. doi: 10.3109/19401736.2015.1060417. Epub 2015 Aug 10. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26258512
Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.
Maalej M, Tej A, Bouguila J, Tilouche S, Majdoub S, Khabou B, Tabbebi M, Felhi R, Ammar M, Mkaouar-Rebai E, Keskes L, Boughamoura L, Fakhfakh F. Maalej M, et al. Among authors: bouguila j. Biochem Biophys Res Commun. 2018 Jan 8;495(2):1730-1737. doi: 10.1016/j.bbrc.2017.12.011. Epub 2017 Dec 5. Biochem Biophys Res Commun. 2018. PMID: 29217198
Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population.
Ben Charfeddine I, Ben Lazreg T, M'sakni A, Amara A, Mlika A, Chaïeb A, Hlel K, Zouari N, Zbidi F, Bouguila J, Soyah N, Ayedi A, Ben Hamouda H, Abroug S, Boughamoura L, Saad A, Gribaa M. Ben Charfeddine I, et al. Among authors: bouguila j. Hemoglobin. 2015;39(4):251-5. doi: 10.3109/03630269.2015.1041605. Epub 2015 May 27. Hemoglobin. 2015. PMID: 26016902
Epidemiology and clinical profile of pathogens responsible for the hospitalization of children in Sousse area, Tunisia.
Brini I, Guerrero A, Hannachi N, Bouguila J, Orth-Höller D, Bouhlel A, Boughamoura L, Hetzer B, Borena W, Schiela B, Von Laer D, Boukadida J, Stoiber H. Brini I, et al. Among authors: bouguila j. PLoS One. 2017 Nov 17;12(11):e0188325. doi: 10.1371/journal.pone.0188325. eCollection 2017. PLoS One. 2017. PMID: 29149199 Free PMC article.
78 results