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Page 1
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS.
Huynh Cong E, Bizet AA, Boyer O, Woerner S, Gribouval O, Filhol E, Arrondel C, Thomas S, Silbermann F, Canaud G, Hachicha J, Ben Dhia N, Peraldi MN, Harzallah K, Iftene D, Daniel L, Willems M, Noel LH, Bole-Feysot C, Nitschké P, Gubler MC, Mollet G, Saunier S, Antignac C. Huynh Cong E, et al. Among authors: hachicha j. J Am Soc Nephrol. 2014 Nov;25(11):2435-43. doi: 10.1681/ASN.2013101126. Epub 2014 May 29. J Am Soc Nephrol. 2014. PMID: 24876116 Free PMC article.
Autosomal dominant Alport's syndrome: study of a large Tunisian family.
Kharrat M, Makni S, Makni K, Kammoun K, Charfeddine K, Azaeiz H, Jarraya F, Ben Hmida M, Gubler MC, Ayadi H, Hachicha J. Kharrat M, et al. Among authors: hachicha j. Saudi J Kidney Dis Transpl. 2006 Sep;17(3):320-5. Saudi J Kidney Dis Transpl. 2006. PMID: 16970251
Cancers after renal transplantation: multicenter experience.
Harzallah K, Abderrahim E, Chareffedine K, Yeich S, Belhadj R, Skhiri H, Younsi F, Abdallah TB, Abdelletif A, Hachicha J, Hmida J, El May M, Khedr A, Manaa J. Harzallah K, et al. Among authors: hachicha j. Saudi J Kidney Dis Transpl. 2008 Sep;19(5):825-30. Saudi J Kidney Dis Transpl. 2008. PMID: 18711309
Short- and long-term outcomes of kidney donors: a report from Tunisia.
Helal I, Abdallah TB, Ounissi M, Tahar G, Cherif M, Boubaker K, Karoui C, Hamida FB, Adberrahim E, El Younsi F, Kheder A, Sfaxi M, Derouiche A, Chebil M, Hachicha J, Mehiri MN, Skhiri H, Elmay M, Harzallah K, Elmanaa MJ, Hmida J. Helal I, et al. Among authors: hachicha j. Saudi J Kidney Dis Transpl. 2012 Jul;23(4):853-9. doi: 10.4103/1319-2442.98187. Saudi J Kidney Dis Transpl. 2012. PMID: 22805410
Crystalline Nephropathy in Renal Transplant: A Series of 4 Cases.
Mnif K, Yaich S, Mars M, Kammoun K, Fendri F, Charfeddine K, Jarraya F, Boudawara T, Hachicha J. Mnif K, et al. Among authors: hachicha j. Indian J Nephrol. 2018 Nov-Dec;28(6):472-476. doi: 10.4103/ijn.IJN_76_17. Indian J Nephrol. 2018. PMID: 30647504 Free PMC article.
[Immunohistochemistry contribution in Alport syndrome diagnosis].
Krichen Makni S, Kharrat M, Ben Hmida M, Chaker H, Gubler MC, Antignac C, Jlidi R, Hachicha J, Sellami Boudwara T. Krichen Makni S, et al. Among authors: hachicha j. Rev Med Interne. 2005 Jul;26(7):583-7. doi: 10.1016/j.revmed.2005.03.012. Rev Med Interne. 2005. PMID: 15936119 French.
A novel de novo splicing mutation c.1444-2A>T in the TSC2 gene causes exon skipping and premature termination in a patient with tuberous sclerosis syndrome.
Abdelwahed M, Touraine R, Ben-Rhouma B, Dhieb D, Mars M, Kammoun K, Hachicha J, Triki C, Kamoun H, Keskes-Ammar L, Belguith N. Abdelwahed M, et al. Among authors: hachicha j. IUBMB Life. 2019 Dec;71(12):1937-1945. doi: 10.1002/iub.2134. Epub 2019 Jul 18. IUBMB Life. 2019. PMID: 31317616 Free article.
115 results