Hadj Kacem H - Search Results

1

Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.

Moalla M, Safi W, Babiker Mansour M, Hadj Kacem M, Mahfood M, Abid M, Kammoun T, Hachicha M, Mnif-Feki M, Hadj Kacem F, Hadj Kacem H. Moalla M, et al. Among authors: hadj kacem m, hadj kacem f, hadj kacem h. Front Endocrinol (Lausanne). 2021 Jul 29;12:684018. doi: 10.3389/fendo.2021.684018. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34393998 Free PMC article. Review.

2

Polymorphisms of HLA DQB1 CAR1/CAR2 and TNFalpha IR2/IR4 microsatellite markers in patients affected with Graves disease.

Maalej A, Hadj Kacem H, Bellassoued M, Abid M, Makni H, Ayadi H. Maalej A, et al. Among authors: hadj kacem h. Clin Immunol. 2000 Aug;96(2):91-3. doi: 10.1006/clim.2000.4881. Clin Immunol. 2000. PMID: 10900155

3

CTLA-4 gene polymorphisms in Tunisian patients with Graves' disease.

Hadj Kacem H, Bellassoued M, Bougacha-Elleuch N, Abid M, Ayadi H. Hadj Kacem H, et al. Clin Immunol. 2001 Dec;101(3):361-5. doi: 10.1006/clim.2001.5121. Clin Immunol. 2001. PMID: 11726229

4

PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study.

Hadj Kacem H, Rebai A, Kaffel N, Masmoudi S, Abid M, Ayadi H. Hadj Kacem H, et al. J Clin Endocrinol Metab. 2003 May;88(5):2274-80. doi: 10.1210/jc.2002-021460. J Clin Endocrinol Metab. 2003. PMID: 12727986

5

Evidence for linkage and association between autoimmune thyroid diseases and the 18q12-q21 region in a large Tunisian family.

Hadj Kacem H, Rebai A, Kaffel N, Abid M, Ayadi H. Hadj Kacem H, et al. Int J Immunogenet. 2006 Feb;33(1):25-32. doi: 10.1111/j.1744-313X.2005.00554.x. Int J Immunogenet. 2006. PMID: 16426239

6

Association and linkage studies of the 20q11.2 region (GRD-2 locus) with Graves' disease in the Tunisian population.

Makni K, Hadj Kacem H, Rebaï A, Abid M, Ayadi H. Makni K, et al. Among authors: hadj kacem h. Ann Hum Biol. 2007 Sep-Oct;34(5):566-72. doi: 10.1080/03014460701479580. Ann Hum Biol. 2007. PMID: 17786592 Free article.

7

Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD).

Belguith-Maalej S, Hadj Kacem H, Rebai A, Mnif M, Abid M, Ayadi H. Belguith-Maalej S, et al. Among authors: hadj kacem h. Immunobiology. 2008;213(7):577-83. doi: 10.1016/j.imbio.2008.01.004. Epub 2008 Mar 4. Immunobiology. 2008. PMID: 18656705

8

Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseases.

Belguith-Maalej S, Hadj-Kacem H, Rebuffat SA, Mnif-Feki M, Nguyen B, Abid M, Gross R, Ayadi H, Peraldi-Roux S. Belguith-Maalej S, et al. Among authors: hadj kacem h. Clin Lab. 2010;56(7-8):335-43. Clin Lab. 2010. PMID: 20857898

9

Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay.

Kallel-Bouattour R, Belguith-Maalej S, Zouari-Bradai E, Mnif M, Abid M, Hadj Kacem H. Kallel-Bouattour R, et al. Among authors: hadj kacem h. Gene. 2017 Jul 15;620:10-14. doi: 10.1016/j.gene.2017.03.043. Epub 2017 Apr 4. Gene. 2017. PMID: 28389359

10

Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.

Tlili A, Al Mutery A, Kamal Eddine Ahmad Mohamed W, Mahfood M, Hadj Kacem H. Tlili A, et al. Among authors: hadj kacem h. Genet Test Mol Biomarkers. 2017 Nov;21(11):686-691. doi: 10.1089/gtmb.2017.0130. Epub 2017 Oct 10. Genet Test Mol Biomarkers. 2017. PMID: 29016196

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