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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Jellouli NK, Hadj Salem I, Ellouz E, Kamoun Z, kamoun F, tlili A, Kaabachi N, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation study. Jellouli NK, et al. J Hum Genet. 2014 Apr;59(4):216-22. doi: 10.1038/jhg.2014.4. Epub 2014 Feb 27. J Hum Genet. 2014. PMID: 24573090
Male hypogonadism and metabolic syndrome.
Naifar M, Rekik N, Messedi M, Chaabouni K, Lahiani A, Turki M, Abid M, Ayedi F, Jamoussi K. Naifar M, et al. Among authors: turki m. Andrologia. 2015 Jun;47(5):579-86. doi: 10.1111/and.12305. Epub 2014 Jul 9. Andrologia. 2015. PMID: 25040289
[TAFRO syndrome and monoclonal gammapathy: Uncommon association!].
Naifar M, Messedi M, Elleuch A, Snoussi M, Gouiaa N, Turki M, Lahiani A, Boudawara T, Bahloul Z, Ayedi F. Naifar M, et al. Among authors: turki m. Curr Res Transl Med. 2016 Jan-Mar;64(1):43-7. doi: 10.1016/j.retram.2016.01.001. Epub 2016 Feb 12. Curr Res Transl Med. 2016. PMID: 27140598 French.
169 results