Landolsi H - 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: landolsi h. 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

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: landolsi h. 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

3

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: landolsi h. Urology. 2011 Oct;78(4):792-6. doi: 10.1016/j.urology.2011.05.049. Epub 2011 Aug 2. Urology. 2011. PMID: 21813165

4

Cytogenetic and molecular aspects of absolute teratozoospermia: comparison between polymorphic and monomorphic forms.

Brahem S, Elghezal H, Ghédir H, Landolsi H, Amara A, Ibala S, Gribaa M, Saad A, Mehdi M. Brahem S, et al. Among authors: landolsi h. Urology. 2011 Dec;78(6):1313-9. doi: 10.1016/j.urology.2011.08.064. Urology. 2011. PMID: 22137696

5

The usefulness of p57(KIP2) immunohistochemical staining and genotyping test in the diagnosis of the hydatidiform mole.

Landolsi H, Missaoui N, Brahem S, Hmissa S, Gribaa M, Yacoubi MT. Landolsi H, et al. Pathol Res Pract. 2011 Aug 15;207(8):498-504. doi: 10.1016/j.prp.2011.06.004. Epub 2011 Jul 20. Pathol Res Pract. 2011. PMID: 21767919

6

NLRP7 mutation analysis in sporadic hydatidiform moles in Tunisian patients: NLRP7 and sporadic mole.

Landolsi H, Rittore C, Philibert L, Hmissa S, Gribaa M, Touitou I, Yacoubi MT. Landolsi H, et al. Arch Pathol Lab Med. 2012 Jun;136(6):646-51. doi: 10.5858/arpa.2011-0399-OA. Arch Pathol Lab Med. 2012. PMID: 22646272 Free article.

7

Screening for NLRP7 mutations in familial and sporadic recurrent hydatidiform moles: report of 2 Tunisian families.

Landolsi H, Rittore C, Philibert L, Missaoui N, Hmissa S, Touitou I, Gribaa M, Yacoubi MT. Landolsi H, et al. Int J Gynecol Pathol. 2011 Jul;30(4):348-53. doi: 10.1097/PGP.0b013e31820dc3b0. Int J Gynecol Pathol. 2011. PMID: 21623199

8

Assessment of the role of histopathology and DNA image analysis in the diagnosis of molar and non-molar abortion: a study of 89 cases in the center of Tunisia.

Landolsi H, Missaoui N, Yacoubi MT, Trabelsi A, Rammeh-Rommani S, Hidar S, Gribaa M, Hmissa S, Mokni M. Landolsi H, et al. Pathol Res Pract. 2009;205(11):789-96. doi: 10.1016/j.prp.2009.05.013. Epub 2009 Aug 7. Pathol Res Pract. 2009. PMID: 19665315

9

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.

Parry DA, Logan CV, Hayward BE, Shires M, Landolsi H, Diggle C, Carr I, Rittore C, Touitou I, Philibert L, Fisher RA, Fallahian M, Huntriss JD, Picton HM, Malik S, Taylor GR, Johnson CA, Bonthron DT, Sheridan EG. Parry DA, et al. Among authors: landolsi h. Am J Hum Genet. 2011 Sep 9;89(3):451-8. doi: 10.1016/j.ajhg.2011.08.002. Epub 2011 Sep 1. Am J Hum Genet. 2011. PMID: 21885028 Free PMC article.

10

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.

Reddy R, Akoury E, Phuong Nguyen NM, Abdul-Rahman OA, Dery C, Gupta N, Daley WP, Ao A, Landolsi H, Ann Fisher R, Touitou I, Slim R. Reddy R, et al. Among authors: landolsi h. Eur J Hum Genet. 2013 Sep;21(9):957-64. doi: 10.1038/ejhg.2012.274. Epub 2012 Dec 12. Eur J Hum Genet. 2013. PMID: 23232697 Free PMC article.

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