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Items: 1 to 20 of 23

1.

Molecular analysis in a GALNS study cohort of 15 Tunisian patients: description of a novel mutation.

Chkioua L, Khedhiri S, Hafsi H, Grissa O, Ben Turkia H, Miled A, Laradi S, Froissart R, Alif N.

Diagn Pathol. 2016 Jun 17;11(1):51. doi: 10.1186/s13000-016-0498-y.

2.

Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene.

Chkioua L, Khedhiri S, Grissa O, Aloui C, Turkia HB, Ferchichi S, Miled A, Froissart R, Acquaviva C, Laradi S.

Meta Gene. 2015 Jul 25;5:144-9. doi: 10.1016/j.mgene.2015.07.003.

3.

Mutations and polymorphisms in N-acetylgalactosamine-6-sulfate sulfatase gene in Turkish Morquio A patients.

Khedhiri S, Chkioua L, Elcioglu N, Laradi S, Miled A.

Pathol Biol (Paris). 2014 Feb;62(1):38-40. doi: 10.1016/j.patbio.2013.10.001.

PMID:
24411403
4.

Low erythrocyte catalase enzyme activity is correlated with high serum total homocysteine levels in Tunisian patients with acute myocardial infarction.

Noichri Y, Chalghoum A, Chkioua L, Baudin B, Ernez S, Ferchichi S, Miled A.

Diagn Pathol. 2013 Apr 30;8:68. doi: 10.1186/1746-1596-8-68.

5.

[Metabolic interactions between the hyperhomocysteinemia and angiotensin-1 converting enzyme activity in Tunisian patients with coronary heart disease].

Chalghoum A, Noichri Y, Chkioua L, Gammoudi I, Dandana A, Khelil S, Jeridi G, Baudin B, Ferchichi S, Miled A.

Ann Biol Clin (Paris). 2012 Oct 1;70(5):599-604. doi: 10.1684/abc.2012.0749. French.

PMID:
23047907
6.

Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease.

Hrira MY, Chkioua L, Slimani A, Chahed H, Mosbah H, Khaldoun HB, Ferchichi S, Addad F, Miled A.

Diagn Pathol. 2012 Jul 26;7(1):88. doi: 10.1186/1746-1596-7-88.

7.

Mucopolysaccharidosis IVA within Tunisian patients: Confirmation of the two novel GALNS gene mutations.

Khedhiri S, Chkioua L, Bouzidi H, Dandana A, Ferchichi S, Ben Turkia H, Miled A, Laradi S.

Pathol Biol (Paris). 2012 Jun;60(3):190-2. doi: 10.1016/j.patbio.2011.03.001.

PMID:
22078177
8.

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population.

Chkioua L, Khedhiri S, Ben Turkia H, Chahed H, Ferchichi S, Ben Dridi MF, Laradi S, Miled A.

Diagn Pathol. 2011 Nov 10;6:113. doi: 10.1186/1746-1596-6-113.

9.

[Morquio A disease: clinical and molecular study of Tunisian patients].

Khedhiri S, Chkioua L, Ferchichi S, Miled A, Laradi S.

Ann Biol Clin (Paris). 2011 Jul-Aug;69(4):425-9. doi: 10.1684/abc.2011.0593. French.

10.

Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients.

Chkioua L, Khedhiri S, Turkia HB, Tcheng R, Froissart R, Chahed H, Ferchichi S, Ben Dridi MF, Vianey-Saban C, Laradi S, Miled A.

Diagn Pathol. 2011 Jun 3;6:47. doi: 10.1186/1746-1596-6-47.

11.

Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II.

Chkioua L, Khedhiri S, Ferchichi S, Tcheng R, Chahed H, Froissart R, Vianey-Saban C, Laradi S, Miled A.

Diagn Pathol. 2011 May 23;6:42. doi: 10.1186/1746-1596-6-42.

12.

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms.

Chkioua L, Khedhiri S, Kassab A, Bibi A, Ferchichi S, Froissart R, Vianey-Saban C, Laradi S, Miled A.

Diagn Pathol. 2011 Apr 26;6:39. doi: 10.1186/1746-1596-6-39.

13.

[Study of the intronic polymorphism of the angiotensin 1 converting enzyme among coronary Tunisians].

Chalghoum A, Noichri Y, Chkioua L, Gammoudi I, Dandana A, Chahed H, Khelil S, Jeridi G, Baudin B, Ferchichi S, Miled A.

Ann Cardiol Angeiol (Paris). 2011 Jun;60(3):135-40. doi: 10.1016/j.ancard.2010.12.019. French.

PMID:
21277558
14.

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: implication in Morquio A disease.

Khedhiri S, Chkioua L, Ferchichi S, Miled A, Laradi S.

Diagn Pathol. 2011 Jan 20;6:11. doi: 10.1186/1746-1596-6-11.

15.

Mucopolysaccharidoses type I and IVA: clinical features and consanguinity in Tunisia.

Khedhiri S, Chkioua L, Bouzidi H, Dandana A, Ben Turkia H, Miled A, Laradi S.

Pathol Biol (Paris). 2009 Jul;57(5):392-7. doi: 10.1016/j.patbio.2008.05.005.

PMID:
18584975
16.

[Molecular analysis of the p.Asn 370 Ser mutation in Gaucher disease].

Dandana A, Ferchichi S, Ben Khelifa S, Jaidane Z, Monastiri K, Chkioua L, Maire I, Froissart R, Bonnet V, Laradi S, Miled A.

Pathol Biol (Paris). 2008 Mar;56(2):88-93. doi: 10.1016/j.patbio.2007.09.029. French.

PMID:
18178337
17.

[Biochemical and molecular diagnosis of Gaucher disease in Tunisia].

Dandana A, Ferchichi S, Khedhiri S, Chkioua L, Jaidane Z, Monastiri K, Ben Khelifa S, Ben Mansour R, Maire I, Froissart R, Bonnet V, Laradi S, Miled A.

Ann Biol Clin (Paris). 2007 Nov-Dec;65(6):647-52. French.

18.

[Mucopolysaccharidosis type I: identification of alpha-L-iduronidase mutations in Tunisian families].

Chkioua L, Khedhiri S, Jaidane Z, Ferchichi S, Habib S, Froissart R, Bonnet V, Chaabouni M, Dandana A, Jrad T, Limem H, Maire I, Abdelhedi M, Laradi S.

Arch Pediatr. 2007 Oct;14(10):1183-9. French.

PMID:
17728118
19.

[Diagnostic strategy of mucopolysaccharidosis type I in Tunisia].

Chkioua L, Ferchichi S, Khedhiri S, Laradi S, Bibi A, Amira D, Dandana A, Ben Mansour R, Ben Limam H, Chaabouni M, Froissart R, Maire I, Miled A.

Ann Biol Clin (Paris). 2007 Mar-Apr;65(2):175-9. French.

20.

[Clinical, biologic and molecular characteristics of two Tunisian MPS IV A patients].

Khedhiri S, Chkioua L, Ferchichi S, Bouzidi H, Haj Khelil A, Ben Mansour R, Kassab A, M'dallah S, Chaabouni M, Jrad T, Ben Chibani J, Miled A, Laradi S.

Ann Biol Clin (Paris). 2007 Jan-Feb;65(1):59-63. French.

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