Mougou S[au] - Search Results

Year	Number of Results
2004	1
2007	2
2011	1
2012	3
2013	3
2014	1
2015	3
2016	1
2017	1
2022	1
2023	3
2024	0

1

[Bilateral microphthalmos and colobomatous cyst of the orbit in a young adult].

Oueslati M, Ghachem M, Tlili T, Mougou S, Knani L. Oueslati M, et al. Among authors: mougou s. J Fr Ophtalmol. 2023 Jan;46(1):e18-e20. doi: 10.1016/j.jfo.2022.06.016. Epub 2022 Dec 7. J Fr Ophtalmol. 2023. PMID: 36496295 French. No abstract available.

2

Factors associated with anxiety and depression in men undergoing fertility investigations: a cross-sectional study.

Kooli R, Sallem A, Chebil D, Boussabbeh M, Mohamed BB, Ajina T, Boughzela I, Mougou S, Mehdi M. Kooli R, et al. Among authors: mougou s. BMC Psychol. 2023 Sep 30;11(1):299. doi: 10.1186/s40359-023-01330-z. BMC Psychol. 2023. PMID: 37777800 Free PMC article.

3

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

4

NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.

Bouali N, Francou B, Bouligand J, Lakhal B, Malek I, Kammoun M, Warszawski J, Mougou S, Saad A, Guiochon-Mantel A. Bouali N, et al. Among authors: mougou s. Clin Genet. 2016 May;89(5):608-13. doi: 10.1111/cge.12750. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26848058

5

New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family.

Bouali N, Francou B, Bouligand J, Imanci D, Dimassi S, Tosca L, Zaouali M, Mougou S, Young J, Saad A, Guiochon-Mantel A. Bouali N, et al. Among authors: mougou s. Fertil Steril. 2017 Oct;108(4):694-702. doi: 10.1016/j.fertnstert.2017.07.015. Epub 2017 Aug 30. Fertil Steril. 2017. PMID: 28863940 Free article.

6

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.

7

Assessment of MYCN amplification status in Tunisian neuroblastoma: CISH and MLPA combining approach.

H'Mida Ben Brahim D, Trabelsi S, Chabchoub I, Gargouri I, Harrabi I, Moussa A, Chourabi M, Haddaji M, Sassi S, Mougou S, Gribaa M, Ben Ahmed S, Zakhama A, Nouri A, Saad A. H'Mida Ben Brahim D, et al. Among authors: mougou s. Tunis Med. 2015 Aug-Sep;93(8-9):527-31. Tunis Med. 2015. PMID: 26815518 Free article.

8

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

9

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

10

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

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