Braham R - Search Results

1

Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype.

Ojeda D, Lakhal B, Fonseca DJ, Braham R, Landolsi H, Mateus HE, Restrepo CM, Elghezal H, Saâd A, Laissue P. Ojeda D, et al. Among authors: braham r. Fertil Steril. 2011 Jun 30;95(8):2658-60.e1. doi: 10.1016/j.fertnstert.2011.04.045. Epub 2011 May 14. Fertil Steril. 2011. PMID: 21575944 Free article.

2

Screening for mutations of the FOXO4 gene in premature ovarian failure patients.

Fonseca DJ, Garzón E, Lakhal B, Braham R, Ojeda D, Elghezal H, Saâd A, Restrepo CM, Laissue P. Fonseca DJ, et al. Among authors: braham r. Reprod Biomed Online. 2012 Mar;24(3):339-41. doi: 10.1016/j.rbmo.2011.11.017. Epub 2011 Dec 2. Reprod Biomed Online. 2012. PMID: 22285440

3

CITED2 mutations potentially cause idiopathic premature ovarian failure.

Fonseca DJ, Ojeda D, Lakhal B, Braham R, Eggers S, Turbitt E, White S, Grover S, Warne G, Zacharin M, Nevin Lam A, Landolsi H, Elghezal H, Saâd A, Restrepo CM, Fellous M, Sinclair A, Koopman P, Laissue P. Fonseca DJ, et al. Among authors: braham r. Transl Res. 2012 Nov;160(5):384-8. doi: 10.1016/j.trsl.2012.05.006. Epub 2012 Jun 16. Transl Res. 2012. PMID: 22709740

4

A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure.

Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: braham r. Clin Endocrinol (Oxf). 2009 Nov;71(5):752-3. doi: 10.1111/j.1365-2265.2009.03571.x. Epub 2009 May 8. Clin Endocrinol (Oxf). 2009. PMID: 19486016 No abstract available.

5

Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure.

Lakhal B, Ben-Hadj-Khalifa S, Bouali N, Braham R, Hatem E, Saad A. Lakhal B, et al. Among authors: braham r. Gene. 2012 Nov 10;509(2):298-301. doi: 10.1016/j.gene.2012.08.007. Epub 2012 Aug 23. Gene. 2012. PMID: 22951804

6

BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: braham r. Clin Endocrinol (Oxf). 2010 Mar;72(3):425-6. doi: 10.1111/j.1365-2265.2009.03651.x. Epub 2009 Jun 8. Clin Endocrinol (Oxf). 2010. PMID: 19508678 No abstract available.

7

[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. 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.

8

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: braham r. 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.

9

Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders.

Elghezal H, Hidar S, Braham R, Denguezli W, Ajina M, Saâd A. Elghezal H, et al. Among authors: braham r. Fertil Steril. 2006 Dec;86(6):1792-5. doi: 10.1016/j.fertnstert.2006.04.041. Epub 2006 Oct 23. Fertil Steril. 2006. PMID: 17056042 Free article.

10

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: braham r. 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

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