Kahloul N - Search Results

1

[Idiopathic steroid-resistant nephrotic syndrome in child : study of 20 cases].

Chemli J, Boussetta S, Krid S, Kahloul N, Hassayoun S, Zakhama A, Abroug S, Hachicha M, Amri F, Guediche MN, Sfar MT, Essoussi AS, Harbi A. Chemli J, et al. Among authors: kahloul n. Tunis Med. 2011 Jun;89(6):522-8. Tunis Med. 2011. PMID: 21681713 Review. French.

2

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.

Ben Charfeddine I, Riepe FG, Clauser E, Ayedi A, Makni S, Sfar MT, Sboui H, Kahloul N, Ben Hamouda H, Chouchane S, Trimech S, Zouari N, M'Rabet S, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: kahloul n. Gene. 2012 Oct 1;507(1):20-6. doi: 10.1016/j.gene.2012.07.027. Epub 2012 Jul 25. Gene. 2012. PMID: 22841790

3

[Pseudohypoparathyroidism revealed by Fahr syndrome].

Kahloul N, Chaari W, Boughamoura L, Charfeddine L, Khammeri S, Amri F. Kahloul N, et al. Arch Pediatr. 2009 May;16(5):444-8. doi: 10.1016/j.arcped.2009.02.017. Epub 2009 Apr 1. Arch Pediatr. 2009. PMID: 19339164 French.

4

[Esophageal cervical duplication revealed by stridor: a case report].

Kahloul N, Mabrouk S, Boughamoura L, Bouguezzi R, Amri F. Kahloul N, et al. Arch Pediatr. 2009 Aug;16(8):1129-32. doi: 10.1016/j.arcped.2009.04.010. Arch Pediatr. 2009. PMID: 19482460 French.

5

[Fetus in fetu: a case report].

Kahloul N, Adouani M, Khattat N, Allani H, Krichen I, Zakhama A, Amri F. Kahloul N, et al. Arch Pediatr. 2010 Mar;17(3):249-52. doi: 10.1016/j.arcped.2009.10.028. Epub 2010 Jan 29. Arch Pediatr. 2010. PMID: 20116220 French.

6

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family.

Ben Charfeddine I, Riepe FG, Kahloul N, Kulle AE, Adala L, Mamaï O, Amara A, Mili A, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: kahloul n. Gen Comp Endocrinol. 2012 Feb 1;175(3):514-8. doi: 10.1016/j.ygcen.2011.12.017. Epub 2011 Dec 22. Gen Comp Endocrinol. 2012. PMID: 22210247

7

[Coronary artery aneurysm in Kawasaki disease and its risk factors : a retrospective study about 65 Tunisian children].

Ajmi H, Ghorbel S, Ezzi O, Mabrouk S, Mansour K, Kahloul N, Chemli J, Zouari N, Mejaouel H, Boughammoura L, Abroug S. Ajmi H, et al. Among authors: kahloul n. Ann Cardiol Angeiol (Paris). 2022 Apr;71(2):86-89. doi: 10.1016/j.ancard.2021.10.011. Epub 2021 Nov 7. Ann Cardiol Angeiol (Paris). 2022. PMID: 34753596 French.

8

Molecular and phenotypic characterization of ring chromosome 22 in two unrelated patients.

Hannachi H, Mougou S, Benabdallah I, Soayh N, Kahloul N, Gaddour N, Le Lorc'h M, Sanlaville D, El Ghezal H, Saad A. Hannachi H, et al. Among authors: kahloul n. Cytogenet Genome Res. 2013;140(1):1-11. doi: 10.1159/000350785. Epub 2013 Apr 27. Cytogenet Genome Res. 2013. PMID: 23635516

9

Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population.

Aloui C, Chakroun T, Granados V, Jemni-Yacoub S, Fagan J, Khelif A, Kahloul N, Hammami S, Chkioua L, Barlier C, Cognasse F, Laradi S, Garraud O. Aloui C, et al. Among authors: kahloul n. Blood Coagul Fibrinolysis. 2018 Dec;29(8):689-696. doi: 10.1097/MBC.0000000000000779. Blood Coagul Fibrinolysis. 2018. PMID: 30325339

10

Beyens A, Moreno-Artero E, Bodemer C, Cox H, Gezdirici A, Yilmaz Gulec E, Kahloul N, Khau Van Kien P, Ogur G, Harroche A, Vasse M, Salhi A, Symoens S, Hadj-Rabia S, Callewaert B. Beyens A, et al. Among authors: kahloul n. Exp Dermatol. 2019 Oct;28(10):1142-1145. doi: 10.1111/exd.13723. Epub 2018 Aug 20. Exp Dermatol. 2019. PMID: 29952037

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