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Items: 1 to 20 of 48

1.

A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma.

Khabou B, Trigui A, Boudawara TS, Keskes L, Kamoun H, Barbu V, Fakhfakh F.

Clin Chim Acta. 2019 Jun 7;495:598-605. doi: 10.1016/j.cca.2019.06.007. [Epub ahead of print]

PMID:
31181191
2.

Hypoparathyroidism in children: a study of eight cases.

Maaloul I, Aloulou H, Kmiha S, Belfitouri Y, Kamoun H, Fakhfakh F, Chabchoub I, Kammoun T, Hachicha M.

Tunis Med. 2018 Aug - Sep;96(8-9):472-476.

3.

Altered three-dimensional organization of sperm genome in DPY19L2-deficient globozoospermic patients.

Abdelhedi F, Chalas C, Petit JM, Abid N, Mokadem E, Hizem S, Kamoun H, Keskes L, Dupont JM.

J Assist Reprod Genet. 2019 Jan;36(1):69-77. doi: 10.1007/s10815-018-1342-y. Epub 2018 Oct 25.

PMID:
30362053
4.

Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene.

Abdelwahed M, Hilbert P, Ahmed A, Mahfoudh H, Bouomrani S, Dey M, Hachicha J, Kamoun H, Keskes-Ammar L, Belguith N.

Gene. 2018 May 31. pii: S0378-1119(18)30623-1. doi: 10.1016/j.gene.2018.05.112. [Epub ahead of print]

PMID:
29860066
5.

A novel TBX1 missense mutation in patients with syndromic congenital heart defects.

Jaouadi A, Tabebi M, Abdelhedi F, Abid D, Kamoun F, Chabchoub I, Maatoug S, Doukali H, Belghuith N, Ksentini MA, Keskes LA, Triki C, Hachicha M, Kamoun S, Kamoun H.

Biochem Biophys Res Commun. 2018 May 15;499(3):563-569. doi: 10.1016/j.bbrc.2018.03.190. Epub 2018 Mar 28.

PMID:
29596833
6.

Association study of apoptosis gene polymorphisms in mitochondrial diabetes: A potential role in the pathogenicity of MD.

Tabebi M, Khabou B, Boukadi H, Ben Hamad M, Ben Rhouma B, Tounsi S, Maalej A, Kamoun H, Keskes-Ammar L, Abid M, Mnif M, Fakhfakh F.

Gene. 2018 Jan 10;639:18-26. doi: 10.1016/j.gene.2017.09.063. Epub 2017 Oct 4.

PMID:
28987347
7.

Cytogenetic monitoring of hospital staff exposed to ionizing radiation: optimize protocol considering DNA repair genes variability.

Doukali H, Ben Salah G, Ben Rhouma B, Hajjaji M, Jaouadi A, Belguith-Mahfouth N, Masmoudi ML, Ammar-Keskes L, Kamoun H.

Int J Radiat Biol. 2017 Nov;93(11):1283-1288. doi: 10.1080/09553002.2017.1377361. Epub 2017 Sep 21.

PMID:
28880740
8.

Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiation.

Doukali H, Ben Salah G, Hamdaoui L, Hajjaji M, Tabebi M, Ammar-Keskes L, Masmoudi ME, Kamoun H.

Int J Radiat Biol. 2017 Jul;93(7):697-704. doi: 10.1080/09553002.2017.1305132. Epub 2017 Apr 11.

PMID:
28287017
9.

Oral care in ventilated intensive care unit patients: Observing nursing behavior through standardization of oral hygiene tool placement.

Diaz TL, Zanone SJ, Charmo-Smith C, Kamoun H, Barrais AI.

Am J Infect Control. 2017 May 1;45(5):559-561. doi: 10.1016/j.ajic.2016.12.008. Epub 2017 Jan 23.

PMID:
28126261
10.

Abstracts of the Communications of the Sixteenth Francophone Allergology Meetings Hammamet, 4-7 October 2017.

Abdelghani A, Abouda M, Adelmoulah K, Aichaouia C, Ajmi N, Akad A, Akrout I, Ammar J, Amouri Z, Aouadi S, Aouina H, Aounallah A, Atitallah S, Ayadi H, Ayadi N, Ayadi S, Azzabi S, Baccar MA, Bahloul N, Bdira B, Bejar D, Beji M, Belajouza C, Belhadj I, Belhaja R, Ben Abdelghaffar H, Ben Amar J, Ben Jemia E, Ben Mahmoud L, Ben Mansour A, Ben Romdhane M, Ben Saad A, Ben Saad H, Ben Saad S, Ben Salah N, Ben Salem N, Ben Tkhayat A, Benzarti M, Berraïes A, Besma H, Bouakkez H, Bouhoula M, Boussetta K, Boussoffara L, Bouzekri H, Brahem A, Brini I, Chaouech N, Charfeddine I, Charfi MR, Charrad R, Chatti S, Cheikh R, Cheikh M'hamed S, Cheikh Rouhou S, Cherif H, Cherif J, Dabboussi S, Daghfous H, Daghfous J, Dahmouni A, Denguezli M, Dhahri B, Djaman Allico J, Douik El Gharbi L, El Gharbi L, El Guedr S, El Kamel A, El Maalel O, Elfekih L, Essalah M, Fahem N, Fessi R, Fki W, Gammoudi R, Garrouch A, Ghariani N, Gharsalli H, Ghedira H, Ghorbel A, Ghozzi H, Ghrairi N, Greb D, Gribaa Y, Guedri S, Gueriani A, Guermazi E, Habouria C, Hadj Hassine S, Hajjej S, Hamdi B, Hamdia B, Hammami A, Hamouda S, Hamzaoui A, Hamzaoui K, Hassen H, Hayouni M, Hedhli A, Houaneb Marghli Y, Jdidi S, Joober S, Kaabachi W, Kacem I, Kaddoussi R, Kalboussi H, Kallel N, Kallel S, Kammoun S, Kamoun H, Kchouk H, Ketata W, Khadhraoui M, Khalsi F, Khattab A, Khbou A, Khessain Z, Khessari Z, Khmekhem R, Khouaja I, Khouani H, Khssairi Z, Kpan Sea E, Kwas H, Lahmer O, Loued L, Louhaichi S, Louzir B, M'saad S, Maalej S, Maazaoui S, Maoua M, Masmoudi D, Mbarek NH, Megdiche ML, Mehiri N, Mejri I, Mhamdi S, Mjid M, Mkaouar N, Moatemri Z, Mokni S, Mrizak N, N'guessan JD, Nouira R, Ouahchi Y, Oujani S, Raies S, Rouatbi S, Rouetbi N, Rouis H, Sakka D, Salhi M, Slama M, Smadhi H, Snene H, Souissi N, Tabboubi A, Tinsa F, Toujeni S, Trigui G, Triki M, Tritar F, Yalaoui S, Yangui F, Yangui I, Yapo-Crezoit C, Zaibi H, Zaim A, Zayani I, Zayen K, Zendah I.

Tunis Med. 2017 Aug - Sep;95(8-9):806-836. No abstract available.

11.

Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.

Tabebi M, Charfi N, Kallabi F, Alila-Fersi O, Ben Mahmoud A, Tlili A, Keskes-Ammar L, Kamoun H, Abid M, Mnif M, Fakhfakh F.

J Diabetes Complications. 2017 Jan;31(1):253-259. doi: 10.1016/j.jdiacomp.2016.06.028. Epub 2016 Jul 1.

PMID:
27422531
12.

Splicing Defects in the AAAS Gene Leading to both Exon Skipping and Partial Intron Retention in a Tunisian Patient with Allgrove Syndrome.

Kallabi F, Ben Rhouma B, Baklouti S, Ghorbel R, Felhi R, Keskes L, Kamoun H.

Horm Res Paediatr. 2016;86(2):90-93. Epub 2016 Jul 15.

PMID:
27414811
13.

A de-novo large deletion of 2.8 kb produced in the ABCD1 gene causing adrenoleukodystrophy disease.

Kallabi F, Ben Salah G, Ben Chehida A, Tabebi M, Felhi R, Ben Turkia H, Tebib N, Keskes L, Kamoun H.

Biochem Cell Biol. 2016 Jun;94(3):265-9. doi: 10.1139/bcb-2015-0168. Epub 2016 Mar 18.

PMID:
27248780
14.

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.

Kallabi F, Belghuith N, Aloulou H, Kammoun T, Ghorbel S, Hajji M, Gallas S, Chemli J, Chabchoub I, Azzouz H, Ben Chehida A, Sfaihi L, Makni S, Amouri A, Keskes L, Tebib N, Ben Becher S, Hachicha M, Kamoun H.

Arch Med Res. 2016 Feb;47(2):105-10. doi: 10.1016/j.arcmed.2016.04.004. Epub 2016 Apr 28.

PMID:
27133709
15.

Histopathological, oxidative damage, biochemical, and genotoxicity alterations in hepatic rats exposed to deltamethrin: modulatory effects of garlic (Allium sativum).

Ncir M, Ben Salah G, Kamoun H, Makni Ayadi F, Khabir A, El Feki A, Saoudi M.

Can J Physiol Pharmacol. 2016 Jun;94(6):571-8. doi: 10.1139/cjpp-2015-0477. Epub 2015 Dec 17.

PMID:
26974685
16.

Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect.

Ben Rhouma B, Kallabi F, Mahfoudh N, Ben Mahmoud A, Engeli RT, Kamoun H, Keskes L, Odermatt A, Belguith N.

J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):86-94. doi: 10.1016/j.jsbmb.2016.03.007. Epub 2016 Mar 5.

PMID:
26956191
17.

Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.

Kallabi F, Ellouz E, Tabebi M, Ben Salah G, Kaabechi N, Keskes L, Triki C, Kamoun H.

Clin Chim Acta. 2016 Jan 30;453:141-6. doi: 10.1016/j.cca.2015.12.014. Epub 2015 Dec 12.

PMID:
26686776
18.

Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa.

Kallabi F, Ben Rebeh I, Felhi R, Sellami D, Masmoudi S, Keskes L, Kamoun H.

Horm Res Paediatr. 2016;85(1):18-21. doi: 10.1159/000441653. Epub 2015 Nov 24.

PMID:
26595337
19.

Isolation and characterization of starch from industrial fresh pasta by-product and its potential use in sugar-snap cookie making.

Ellouzi SZ, Driss D, Maktouf S, Neifar M, Kobbi A, Kamoun H, Chaabouni SE, Ghorbel RE.

J Food Sci Technol. 2015 Sep;52(9):5754-62. doi: 10.1007/s13197-014-1567-4. Epub 2014 Dec 6.

20.

Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient.

Kallabi F, Hadj Salem I, Ben Chehida A, Ben Salah G, Ben Turkia H, Tebib N, Keskes L, Kamoun H.

Neurosci Res. 2015 Aug;97:7-12. doi: 10.1016/j.neures.2015.03.005. Epub 2015 Mar 31.

PMID:
25835712

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