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Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment.
Khabou B, Kallabi F, Abdelaziz RB, Maaloul I, Aloulou H, Chehida AB, Kammoun T, Barbu V, Boudawara TS, Fakhfakh F, Khemakhem B, Sahnoun OS. Khabou B, et al. Among authors: aloulou h. Ann Hum Genet. 2024 May;88(3):194-211. doi: 10.1111/ahg.12542. Epub 2023 Dec 18. Ann Hum Genet. 2024. PMID: 38108658
[Rheumatic cardiopathies and its risk factors: about 50 cases].
Maaloul I, Bouzidi N, Kolsi R, Ameur SB, Abid L, Aloulou H, Kamoun T. Maaloul I, et al. Among authors: aloulou h. Ann Cardiol Angeiol (Paris). 2024 Feb;73(1):101676. doi: 10.1016/j.ancard.2023.101676. Epub 2023 Nov 20. Ann Cardiol Angeiol (Paris). 2024. PMID: 37988890 French.
[General practitioners' management of childhood asthma in Sfax, Tunisia].
Ben Ameur S, Elasmar K, Jdidi J, Belhadj R, Aloulou H, Maaloul I, Damak J, Kammoun T. Ben Ameur S, et al. Among authors: aloulou h. Rev Mal Respir. 2022 Dec;39(10):839-847. doi: 10.1016/j.rmr.2022.09.006. Epub 2022 Oct 20. Rev Mal Respir. 2022. PMID: 36272855 French.
Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys.
Said MB, Ayed IB, Elloumi I, Hasnaoui M, Souissi A, Idriss N, Aloulou H, Chabchoub I, Maâlej B, Driss D, Masmoudi S. Said MB, et al. Among authors: aloulou h. Mol Genet Genomic Med. 2022 Feb;10(2):e1868. doi: 10.1002/mgg3.1868. Epub 2022 Jan 8. Mol Genet Genomic Med. 2022. PMID: 34997822 Free PMC article.
72 results