Saad A - Search Results

1

Novel human pathological mutations. Gene symbol: SRY. Disease: XY sex reversal.

Ravel C, Lakhal B, Elghezal H, Braham R, Saad A, Bashamboo A, Siffroi JP, McElreavey K, Christin-Maitre S. Ravel C, et al. Among authors: saad a. Hum Genet. 2009 Aug;126(2):333. Hum Genet. 2009. PMID: 19694000 No abstract available.

2

Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.

Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, Elghezal H, Philibert P, Saâd A, Sultan C, Fellous M, Veitia RA. Laissue P, et al. Among authors: saad a. J Med Genet. 2009 Jul;46(7):455-7. doi: 10.1136/jmg.2008.065086. Epub 2009 May 7. J Med Genet. 2009. PMID: 19429596 Free article.

3

Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients.

Lakhal B, Braham R, Berguigua R, Bouali N, Zaouali M, Chaieb M, Veitia RA, Saad A, Elghezal H. Lakhal B, et al. Among authors: saad a. Clin Genet. 2010 Aug;78(2):181-5. doi: 10.1111/j.1399-0004.2009.01359.x. Epub 2009 Dec 2. Clin Genet. 2010. PMID: 20345472

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: saad a. Clin Genet. 2016 May;89(5):608-13. doi: 10.1111/cge.12750. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26848058

5

[Place of pelvic ultrasonography using transabdominal technique in the investigation of premature ovarian failure].

Braham R, Hidar S, Chaieb M, Trimeche S, Zaouali M, Lakhal B, Saâd A, Ach K, Chaieb L, Elghezal H. Braham R, et al. Among authors: saad a. Ann Endocrinol (Paris). 2010 Sep;71(4):286-90. doi: 10.1016/j.ando.2010.03.008. Epub 2010 Jun 2. Ann Endocrinol (Paris). 2010. PMID: 20627259 French.

6

Semen processing by density gradient centrifugation is useful in selecting sperm with higher double-strand DNA integrity.

Brahem S, Mehdi M, Elghezal H, Saad A. Brahem S, et al. Among authors: saad a. Andrologia. 2011 Jun;43(3):196-202. doi: 10.1111/j.1439-0272.2010.01050.x. Epub 2011 Jan 19. Andrologia. 2011. PMID: 21486399

7

Study of aneuploidy rate and sperm DNA fragmentation in large-headed, multiple-tailed spermatozoa.

Brahem S, Mehdi M, Elghezal H, Saad A. Brahem S, et al. Among authors: saad a. Andrologia. 2012 Apr;44(2):130-5. doi: 10.1111/j.1439-0272.2010.01115.x. Epub 2011 Jun 30. Andrologia. 2012. PMID: 21714801

8

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

9

Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX.

Ben Hamouda H, Mkacher N, Elghezal H, Bannour H, Kamoun M, Soua H, Saad A, Souissi MM, Sfar MT. Ben Hamouda H, et al. Among authors: saad a. J Gynecol Obstet Biol Reprod (Paris). 2009 Nov;38(7):599-603. doi: 10.1016/j.jgyn.2009.08.003. Epub 2009 Sep 16. J Gynecol Obstet Biol Reprod (Paris). 2009. PMID: 19762167 Free article.

10

Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man.

Hannachi H, Mougou-Zerelli S, BenAbdallah I, Mama N, Hamdi I, Labalme A, Elghezal H, Sanlaville D, Saad A. Hannachi H, et al. Among authors: saad a. Cytogenet Genome Res. 2011;135(2):102-10. doi: 10.1159/000330880. Epub 2011 Aug 26. Cytogenet Genome Res. 2011. PMID: 21876345

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