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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 1
2007 3
2008 1
2009 1
2010 3
2011 3
2012 1
2013 4
2014 4
2016 1
2018 2
2021 2
2022 3
2023 6
2024 2

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Page 1
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Moalla M, Safi W, Babiker Mansour M, Hadj Kacem M, Mahfood M, Abid M, Kammoun T, Hachicha M, Mnif-Feki M, Hadj Kacem F, Hadj Kacem H. Moalla M, et al. Among authors: kammoun t. Front Endocrinol (Lausanne). 2021 Jul 29;12:684018. doi: 10.3389/fendo.2021.684018. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34393998 Free PMC article. Review.
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation.
Maalej M, Sfaihi L, Ammar M, Frikha F, Kharrat M, Alila-Fersi O, Mkaouar-Rebai E, Tlili A, Kammoun T, Fakhfakh F. Maalej M, et al. Among authors: kammoun t. Neurogenetics. 2022 Oct;23(4):257-270. doi: 10.1007/s10048-022-00696-3. Epub 2022 Jul 11. Neurogenetics. 2022. PMID: 35819538
Hypoparathyroidism in children: a study of eight cases.
Maaloul I, Aloulou H, Kmiha S, Belfitouri Y, Kamoun H, Fakhfakh F, Chabchoub I, Kammoun T, Hachicha M. Maaloul I, et al. Among authors: kammoun t. Tunis Med. 2018 Aug-Sep;96(8-9):472-476. Tunis Med. 2018. PMID: 30430523
A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.
Aguech A, Sfaihi L, Alila-Fersi O, Kolsi R, Tlili A, Kammoun T, Fendri A, Fakhfakh F. Aguech A, et al. Among authors: kammoun t. Metab Brain Dis. 2023 Dec;38(8):2665-2678. doi: 10.1007/s11011-023-01276-6. Epub 2023 Sep 1. Metab Brain Dis. 2023. PMID: 37656370
31 results