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Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.
Ghedira N, Lagarde A, Ben Ameur K, Elouej S, Sakka R, Kerkeni E, Chioukh FZ, Olschwang S, Desvignes JP, Abdelhak S, Delague V, Lévy N, Monastiri K, De Sandre-Giovannoli A. Ghedira N, et al. Among authors: monastiri k. BMC Pediatr. 2018 Aug 29;18(1):286. doi: 10.1186/s12887-018-1259-8. BMC Pediatr. 2018. PMID: 30157809 Free PMC article.
Molecular characterization of piebaldism in a Tunisian family.
Kerkeni E, Boubaker S, Sfar S, Bizid M, Besbes H, Bouaziz S, Ghedira N, Amara A, Manoubi W, Gribaa M, Monastiri K. Kerkeni E, et al. Among authors: monastiri k. Pathol Biol (Paris). 2015 Jun;63(3):113-6. doi: 10.1016/j.patbio.2015.03.004. Epub 2015 Apr 21. Pathol Biol (Paris). 2015. PMID: 25910686
Sanjad-Sakati syndrome in a Tunisian child.
Kerkeni E, Sakka R, Sfar S, Bouaziz S, Ghedira N, Ben Ameur K, Ben Hmida H, Chioukh FZ, Ghédira ES, Gribaa M, Monastiri K. Kerkeni E, et al. Among authors: monastiri k. Arch Pediatr. 2015 Sep;22(9):951-5. doi: 10.1016/j.arcped.2015.06.003. Epub 2015 Jul 29. Arch Pediatr. 2015. PMID: 26231322
Comorbidity in the Tunisian population.
Romdhane L, Messaoud O, Bouyacoub Y, Kerkeni E, Naouali C, Cherif Ben Abdallah L, Tiar A, Charfeddine C, Monastiri K, Chabchoub I, Hachicha M, Tadmouri GO, Romeo G, Abdelhak S. Romdhane L, et al. Among authors: monastiri k. Clin Genet. 2016 Mar;89(3):312-9. doi: 10.1111/cge.12616. Epub 2015 Jun 10. Clin Genet. 2016. PMID: 26010040
[Neonatal hyperthyroidism and maternal Graves disease].
Ben Ameur K, Chioukh FZ, Marmouch H, Ben Hamida H, Bizid M, Monastiri K. Ben Ameur K, et al. Among authors: monastiri k. Arch Pediatr. 2015 Apr;22(4):387-9. doi: 10.1016/j.arcped.2015.01.006. Epub 2015 Feb 26. Arch Pediatr. 2015. PMID: 25727474 French.
77 results