Mougou S - Search Results

1

Response to growth hormone therapy in ring chromosome 15: Review and evidence from a new case on possible beneficial effect in neurodevelopment.

Wannes S, El Ahmer I, Rjiba K, Jemmali N, Abdallah HH, Haj RB, Achour A, Bouzidi H, Saad A, Mougou S, Mahjoub B. Wannes S, et al. Among authors: mougou s. Growth Horm IGF Res. 2023 Aug;71:101550. doi: 10.1016/j.ghir.2023.101550. Epub 2023 Jul 25. Growth Horm IGF Res. 2023. PMID: 37531800

2

Large duplication 4q25-q34 with mild clinical effect.

Elghezal H, Sendi HS, Monastiri K, Lapierre JM, Romdhane SI, Mougou S, Saad A. Elghezal H, et al. Among authors: mougou s. Ann Genet. 2004 Oct-Dec;47(4):419-22. doi: 10.1016/j.anngen.2004.07.007. Ann Genet. 2004. PMID: 15581841

3

Prevalence of chromosomal abnormalities in couples with recurrent miscarriage.

Elghezal H, Hidar S, Mougou S, Khairi H, Saâd A. Elghezal H, et al. Among authors: mougou s. Fertil Steril. 2007 Sep;88(3):721-3. doi: 10.1016/j.fertnstert.2006.11.160. Epub 2007 Feb 23. Fertil Steril. 2007. PMID: 17320875 Free article.

4

Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.

Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A. Elghezal H, et al. Among authors: mougou s. Eur J Med Genet. 2007 Nov-Dec;50(6):441-5. doi: 10.1016/j.ejmg.2007.07.002. Epub 2007 Aug 6. Eur J Med Genet. 2007. PMID: 17851150

5

Semen parameters and sperm DNA fragmentation as causes of recurrent pregnancy loss.

Brahem S, Mehdi M, Landolsi H, Mougou S, Elghezal H, Saad A. Brahem S, et al. Among authors: mougou s. Urology. 2011 Oct;78(4):792-6. doi: 10.1016/j.urology.2011.05.049. Epub 2011 Aug 2. Urology. 2011. PMID: 21813165

6

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.

Ben-Abdallah-Bouhjar I, Hannachi H, Labalme A, Gmidène A, Mougou S, Soyah N, Gribaa M, Sanlaville D, Elghezal H, Saad A. Ben-Abdallah-Bouhjar I, et al. Among authors: mougou s. Eur J Med Genet. 2012 Aug-Sep;55(8-9):461-5. doi: 10.1016/j.ejmg.2012.04.011. Epub 2012 Jun 7. Eur J Med Genet. 2012. PMID: 22683462

7

A combination of micronucleus assay and fluorescence in situ hybridization analysis to evaluate the genotoxicity of formaldehyde.

Bouraoui S, Mougou S, Brahem A, Tabka F, Ben Khelifa H, Harrabi I, Mrizek N, Elghezal H, Saad A. Bouraoui S, et al. Among authors: mougou s. Arch Environ Contam Toxicol. 2013 Feb;64(2):337-44. doi: 10.1007/s00244-012-9828-6. Epub 2012 Nov 8. Arch Environ Contam Toxicol. 2013. PMID: 23132144

8

A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers.

Bouraoui S, Mougou S, Drira A, Tabka F, Bouali N, Mrizek N, Elghezal H, Saad A. Bouraoui S, et al. Among authors: mougou s. Int J Occup Med Environ Health. 2013 Mar;26(1):144-54. doi: 10.2478/s13382-013-0084-4. Epub 2013 Apr 4. Int J Occup Med Environ Health. 2013. PMID: 23559140 Free article.

9

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: mougou s. Cytogenet Genome Res. 2013;140(1):1-11. doi: 10.1159/000350785. Epub 2013 Apr 27. Cytogenet Genome Res. 2013. PMID: 23635516

10

Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor.

H'mida Ben-Brahim D, Hammami S, Haddaji Mastouri M, Trabelsi S, Chourabi M, Sassi S, Mougou S, Gribaa M, Zakhama A, Guédiche MN, Saad A. H'mida Ben-Brahim D, et al. Among authors: mougou s. Appl Transl Genom. 2014 Oct 15;4:1-3. doi: 10.1016/j.atg.2014.10.001. eCollection 2015 Mar. Appl Transl Genom. 2014. PMID: 26937341 Free PMC article.

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